The DOI matches its Crossref record; 22 of the 22 references it cites were found in a registry or an index; 7 of the 15 sources its claims cite were checked for support.
Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression
Open accessAbstract
BACKGROUND: Psilocybin is being studied for use in treatment-resistant depression. METHODS: In this phase 2 double-blind trial, we randomly assigned adults with treatment-resistant depression to receive a single dose of a proprietary, synthetic formulation of psilocybin at a dose of 25 mg, 10 mg, or 1 mg (control), along with psychological support. The primary end point was the change from baseline to week 3 in the total score on the Montgomery-Åsberg Depression Rating Scale (MADRS; range, 0 to 60, with higher scores indicating more severe depression). Secondary end points included response at week 3 (≥50% decrease from baseline in the MADRS total score), remission at week 3 (MADRS total score ≤10), and sustained response at 12 weeks (meeting response criteria at week 3 and all subsequent visits). RESULTS: A total of 79 participants were in the 25-mg group, 75 in the 10-mg group, and 79 in the 1-mg group. The mean MADRS total score at baseline was 32 or 33 in each group. Least-squares mean changes from baseline to week 3 in the score were -12.0 for 25 mg, -7.9 for 10 mg, and -5.4 for 1 mg; the difference between the 25-mg group and 1-mg group was -6.6 (95% confidence interval [CI], -10.2 to -2.9; P<0.001) and between the 10-mg group and 1-mg group was -2.5 (95% CI, -6.2 to 1.2; P = 0.18). In the 25-mg group, the incidences of response and remission at 3 weeks, but not sustained response at 12 weeks, were generally supportive of the primary results. Adverse events occurred in 179 of 233 participants (77%) and included headache, nausea, and dizziness. Suicidal ideation or behavior or self-injury occurred in all dose groups. CONCLUSIONS: In this phase 2 trial involving participants with treatment-resistant depression, psilocybin at a single dose of 25 mg, but not 10 mg, reduced depression scores significantly more than a 1-mg dose over a period of 3 weeks but was associated with adverse effects. Larger and longer trials, including comparison with existing treatments, are required to determine the efficacy and safety of psilocybin for this disorder. (Funded by COMPASS Pathfinder; EudraCT number, 2017-003288-36; ClinicalTrials.gov number, NCT03775200.).
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Claims the paper makes
7 of 15 cited sources checked · 5 supported · 0 flagged · accuracy not yet measured
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Its potential antidepressant efficacy was suggested by preliminary studies involving patients with life-threatening cancer.[5][6][7]”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Abstract
What the sources say
- Not checked — no full text of the sourcecites [5] 5. Grob CS, Danforth AL, Chopra GS, et al. Pilot study of psilocybin treatment for anxiety in patients with advanced- stage cancer. Arch Gen Psychiatry 2011; 68: 71-8. source
- Supportedcites [6] 6. Ross S, Bossis A, Guss J, et al. Rapid and sustained symptom reduction follow- ing psilocybin treatment for anxiety and depression in patients with life-threaten- ing cancer: a randomized controlled trial. J Psychopharmacol 2016; 30: 1165-80. source
The Discussion (Primary outcomes) reports that psilocybin, given with psychotherapy, reduced depression in patients with life-threatening cancer. The Conclusions likewise describe rapid and sustained antidepressant effects while calling for further research to establish efficacy definitively. (LLM, conf=0.93)
- Supportedcites [7] 7. Griffiths RR, Johnson MW, Carducci MA, et al. Psilocybin produces substantial and sustained decreases in depression and anxiety in patients with life-threaten- ing cancer: a randomized double-blind trial. J Psychopharmacol 2016; 30: 1181-97. source
The Discussion reports that high-dose psilocybin decreased depressed mood in patients with a life-threatening cancer diagnosis. The Conclusions describe substantial, enduring decreases under psychologically supportive conditions, supporting the citing sentence’s cautious claim of potential antidepressant efficacy. (LLM, conf=0.94)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesThe cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Amelioration of symptomatic depression in pilot studies of major depressive disorder, including those that compared psilocybin with escitalopram 8,9 and that investigated its use in treatment-resistant depression, 10 has suggested therapeutic potential for this agent.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Abstract
What the sources say
- Partly supportedcites [8] 8. Davis AK, Barrett FS, May DG, et al. Effects of psilocybin-assisted therapy on major depressive disorder: a randomized clinical trial. JAMA Psychiatry 2021; 78: 481-9. sourceExperimental — accuracy not yet measured
The Discussion and Conclusions report reduced depressive symptoms following psilocybin-assisted therapy in patients with major depressive disorder, supporting its therapeutic potential. But the Methods describe a delayed-treatment control, not an escitalopram comparison. The Discussion identifies treatment-resistant depression as the subject of a previous study, not this trial. No page numbers are available in our copy. (LLM, conf=0.88)
- Not checked — no full text of the sourcecites [9] 9. Carhart-Harris R, Giribaldi B, Watts R, et al. Trial of psilocybin versus escital- opram for depression. N Engl J Med 2021; 384: 1402-11. source
- Supportedcites [10] 10. Carhart-Harris RL, Bolstridge M, Rucker J, et al. Psilocybin with psycho- logical support for treatment-resistant depression: an open-label feasibility study. Lancet Psychiatry 2016; 3: 619-27. source
Citation 10 is attached to the treatment-resistant depression study, not the escitalopram comparisons cited as 8 and 9. The paper’s “Added value of this research” section (page not supplied) reports enduring reductions in symptom severity and says psilocybin might have value for treatment-resistant depression. (LLM, conf=0.93)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Pharmacokinetic research has shown dose-dependent increases in receptor occupancy and subjective effects of psilocybin across the dose range of 3 to 30 mg. 18”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Discussion
What the sources say
- Supportedcites [18] 18. Madsen MK, Fisher PM, Burmester D, et al. Psychedelic effects of psilocybin correlate with serotonin 2A receptor oc- cupancy and plasma psilocin levels. Neu- ropsychopharmacology 2019; 44: 1328-34. source
The Discussion states that psilocybin doses of 3–30 mg were associated with dose-dependent cerebral 5-HT2A receptor occupancy. It also reports that subjective intensity ratings were positively correlated with receptor occupancy and plasma psilocin levels, supporting the paraphrase about subjective effects. (LLM, conf=0.88)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Supported
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Before the week 3 primary end-point assessment, initiation of treatment for depression was reported by 4 participants (5%) in the 25-mg group, 9 (12%) in the 10-mg group, and 14 (18%) in the 1-mg group.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > R esult s
Strength:plain· not yet calibratedn = 4Tests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“and the difference between the 10-mg group and the 1-mg group was -2.5 (95% CI, -6.2 to 1.2; P = 0.18)”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Efficacy
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Rests on an assumption: The 1-mg dose of psilocybin is an inactive control that does not itself produce antidepressant effects.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“No serious adverse events were reported from day 2 up to week 3 in the 1-mg group.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Safety
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“There were no serious adverse events reported on day 1.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Safety
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In this trial of psilocybin administered in a single session with psychological support, a 25-mg dose but not a 10-mg dose resulted in a significantly greater reduction (improvement) in MADRS total scores than a 1-mg dose at 3 weeks in participants with treatment-resistant depression but was associated with adverse events.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Discussion
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Rests on an assumption: The 1-mg dose of psilocybin is an inactive comparator that does not produce therapeutic effects.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“included a trial population in which more than 90% of the participants did not have previous exposure to psilocybin”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Discussion
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The confidence interval for the odds ratio for sustained response at week 12 for both the 25-mg dose and the 10-mg dose as compared with the 1-mg dose included 1.”
- Also stated in: § Discussion · plain
“The confidence interval for the odds ratio for sustained response at week 12 for the 25-mggroup as compared with the 1-mg group included 1.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Efficacy
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Also stated in: § Discussion · plain
- Probably not a substantial claim. 18
- It may state two separate claims as one. 30
The cited sources that could be checked couldn’t confirm or dispute this claim.
In the paper
“Patients with treatment-resistant depression have greater severity and duration of illness, disability, physical illness, incidences of hospitalization, risk of suicide, and economic costs than patients with treatment-responsive depression.[1][2][3]”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Abstract
What the sources say
- Not checked — no full text of the sourcecites [1] 1. Rush AJ, Trivedi MH, Wisniewski SR, et al. Acute and longer-term outcomes in depressed outpatients requiring one or several treatment steps: a STAR*D report. Am J Psychiatry 2006; 163: 1905-17. source
- Not checked — no full text of the sourcecites [2] 2. Warden D, Rush AJ, Trivedi MH, Fava M, Wisniewski SR. The STAR*D project results: a comprehensive review of find- ings. Curr Psychiatry Rep 2007; 9: 449-59. source
- Could not verifycites [3] 3. Pigott HE. The STAR*D trial: it is time to reexamine the clinical beliefs that guide the treatment of major depression. Can J Psychiatry 2015; 60: 9-13. sourceExperimental — accuracy not yet measured
The Methods passages discuss STAR*D remission, relapse, and treatment dropout, but do not compare treatment-resistant with treatment-responsive patients on illness burden. Searches for severity, disability, physical illness, hospitalization, suicide, and economic costs found no passage making the claimed comparison in our copy. (LLM, conf=0.74)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
Every source the paper cites for this claim was checked and supports it.
In the paper
“The Structured Interview Guide for the MADRS provided structured probes to ensure standardization of administration and comprehensive coverage of the 10 questions.15”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Efficacy End Points
What the sources say
- Supportedcites [15] 15. Williams JB, Kobak KA. Development and reliability of a structured interview guide for the Montgomery Asberg De- pression Rating Scale (SIGMA). Br J Psy- chiatry 2008; 192: 52-8. source
The ‘Development of SIGMA probes and conventions’ section explicitly says that SIGMA provides structured probes to standardise administration and ensure comprehensive coverage of the scale’s ten items. It also describes questions for each item. (LLM, conf=0.95)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“A total of 79 participants were assigned to the 25-mg group, 75 to the 10-mg group, and 79 to the 1-mg group (Fig. 1).”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > R esult s
Strength:plain· not yet calibratedn = 79Tests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The least-squares mean change from baseline to week 3 in the MADRS total score was -12.0 points in the 25-mg group, -7.9 in the 10-mg group, and -5.4 in the 1-mg group.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Efficacy
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The incidence of response at week 3 was 37% in the 25-mg group, 19% in the 10-mg group, and 18% in the 1-mg group (odds ratio in the 25-mg group vs. the 1-mg group, 2.9 [95% CI, 1.2 to 6.6]; odds ratio in the 10-mg group vs. the 1-mg group, 1.2 [95% CI, 0.5 to 3.0])”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Efficacy
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Rests on an assumption: The 1-mg dose of psilocybin is an inactive control that does not itself produce antidepressant effects.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“After week 3 and up to week 12, the number of participants initiating a treatment for depression was 26 (33%) in the 25-mg group, 18 (24%) in the 10-mg group, and 16 (20%) in the 1-mg group.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > R esult s
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The incidence of remission at week 3 was 29% in the 25-mg group, 9% in the 10-mg group, and 8% in the 1-mg group (odds ratio in the 25-mg group vs. the 1-mg group, 4.8 [95% CI, 1.8 to 12.8]; odds ratio in the 10-mg group vs. the 1-mg group, 1.2 [95% CI, 0.4 to 3.9]).”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Efficacy
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Rests on an assumption: The 1-mg dose of psilocybin is an inactive control that does not itself produce antidepressant effects.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“All three had a history of suicidal behavior or nonsuicidal self-injury before the trial and did not have a treatment response at week 3.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Safety
Tests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The incidence of sustained response at week 12 was 20% in the 25-mg group, 5% in the 10-mg group, and 10% in the 1-mg group (odds ratio in the 25-mg group vs. the 1-mg group, 2.2 [95% CI, 0.9 to 5.4];”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Efficacy
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Rests on an assumption: The 1-mg dose of psilocybin is an inactive control that does not itself produce antidepressant effects.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The serious adverse events in the 25-mg group were suicidal ideation (in two participants) and intentional self-injury (nonsuicidal self-injurious behavior) (in two participants) and in the 10-mg group were suicidal ideation (in two participants), intentional selfinjury (in one participant), and hospitalization (for severe depression, in one participant).”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Safety
Strength:plain· not yet calibratedn = 2Tests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“No clinically significant changes in vital signs, clinical laboratory tests, or 12-lead ECGs were observed during the trial (see the Supplementary Appendix).”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Safety
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The incidences of response and remission at 3 weeks were generally in the same direction as the primary end-point results; however, the analyses of these end points were ordered in the prespecified hierarchical test procedure after the significance testing had terminated, and no definite conclusions can be drawn from these results.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Discussion
Strength:hedged· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The serious adverse events in the 25-mg group were suicidal ideation (in two participants) and intentional self-injury (nonsuicidal self-injurious behavior) (in two participants) and in the 10-mg group were suicidal ideation (in two participants), intentional selfinjury (in one participant), and hospitalization (for severe depression, in one participant).”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Safety
Strength:plain· not yet calibratedn = 2Tests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Adverse events occurred in 179 of 233 participants (77%) and included headache, nausea, and dizziness.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“At the baseline visit, suicidal ideation (passive or active but with no intent or plan) was reported by 21 participants (27%) in the 25-mg group, 27 (36%) in the 10-mg group, and 19 (24%) in the 1-mg group.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Safety
Strength:plain· not yet calibratedn = 21Tests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“After week 3 and up to week 12 (end of trial), severe adverse events were reported by 3% of the participants in the 25-mg group, 4% of those in the 10-mg group, and no participants in the 1-mg group.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Safety
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The number of participants who showed worsening of suicidal state from baseline to week 3 were 11 (14%) in the 25-mg group, 13 (17%) in the 10-mg group, and 7 (9%) in the 1-mg group (Table S8).”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Safety
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Adverse events that were rated as severe on day 1 were reported by 4% of the participants in the 25-mg group, 8% of those in the 10-mg group, and 1% of those in the 1-mg group.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Safety
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Secondary end-point results generally supported the primary analysis with the exception of 12week sustained response, at which time point the observed numerical difference was not considered to be statistically significant.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Discussion
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Just one participant (in the 25-mg group) was treated with adjunctive medication (lorazepam for acute anxiety) on day 1.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Safety
Strength:plain· not yet calibratedSingle caseTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In addition to headache, nausea, dizziness, and fatigue, some participants had suicidal ideation or self-injurious behavior, and the proportions of these participants were numerically higher in the 25-mg and 10-mg groups than in the 1-mg group.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Discussion
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Adverse events occurred in 66 participants (84%) in the 25-mg group, 56 (75%) in the 10-mg group, and 57 (72%) in the 1-mg group.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Safety
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“Efficacy analyses were performed in the modified intention-to-treat analysis set, which included all randomly assigned participants who received treatment and had at least one postbaseline efficacy assessment.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Statistical Analysis
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“This was a phase 2 double-blind, dose-finding, parallel-group, randomized clinical trial.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Trial Oversight
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“The nonsignificant finding for the comparison between the 10-mg group and the 1-mg group terminated significance testing on the basis of the prespecified hierarchical test procedure, and all the subsequent key secondary efficacy end points are considered to be not significantly different between the 25-mg group or the 10-mg group and the 1-mg group.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Efficacy
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“All the therapists were unaware of the trial-group assignments, did not collect efficacy assessments, and were discouraged from speculating about doses.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Trial Design and Procedures
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“To control the overall type I error rate, a hierarchical test procedure was applied across the primary and three key secondary efficacy end points.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Statistical Analysis
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“Ran-domization was performed at a central location and stratified according to country and the participant's previous experience with psilocybin.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Trial Design and Procedures
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“By week 12, a total of 5 participants (6%) in the 25-mg group, 9 (12%) in the 10-mg group, and 10 (13%) in the 1-mg group had withdrawn from the trial.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > R esult s
Strength:plain· not yet calibratedn = 5Tests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“An independent contract research organization (MedAvante-ProPhase) was responsible for assessment of participants using the Montgomery-Åsberg Depression Rating Scale (MADRS), 12 performed by trained remote raters who were unaware of the details of the trial and the trial-group assign-ments.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Trial Oversight
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“These characteristics were similar to what has been observed in population studies involving persons with treatment-resistant depression, and the representativeness of the trial population is shown in Table S11.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > R esult s
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“All the participants provided written informed consent.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Trial Oversight
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“The incidence of response at week 3 of 37% in the 25-mg group in our trial was numerically lower than that described for first-line treatment of major depressive disorder in several large trials of citalopram, 1 nefazodone, and escitalopram, sertraline, or venlafaxine 17 but was higher than the incidences of response reported in the STAR*D trial for second-line treatments and beyond.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Discussion
What the sources say
- Not checked — no full text of the sourcecites [1] 1. Rush AJ, Trivedi MH, Wisniewski SR, et al. Acute and longer-term outcomes in depressed outpatients requiring one or several treatment steps: a STAR*D report. Am J Psychiatry 2006; 163: 1905-17. source
- Not checked — no full text of the sourcecites [17] 17. Saveanu R, Etkin A, Duchemin A-M, et al. The international Study to Predict Optimized Treatment in Depression (iSPOT-D): outcomes from the acute phase of antidepressant treatment. J Psy- chiatr Res 2015; 61: 1-12. source
Strength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The manualized, time-limited approach to preparation, support, and integration of the psychedelic experience ensured safety and is not a stand-alone psychotherapy.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Discussion
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✗ Based: failsProbably not a substantial claim. The paper’s conclusions may not depend on it. The paper may give no reason why it holds. It may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“Limitations of the current trial include the lack of an active comparator, the lack of an ethnically diverse participant sample, and the exclusion of persons judged to be at a clinically significant risk for suicide.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Discussion
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“We did not assess participants' ability to guess their dose assignment, and ensuring blinding is an inherent limitation of studies of drugs that produce psychedelic subjective effects.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Discussion
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“The trial was conducted in accordance with the International Council for Harmonisation (ICH) Good Clinical Practice guidelines and the ethical principles of the Declaration of Helsinki.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Trial Oversight
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In the 25-mg group, the incidences of response and remission at 3 weeks, but not sustained response at 12 weeks, were generally supportive of the primary results.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Rests on an assumption: The 1-mg dose of psilocybin is an inactive control that does not itself produce antidepressant effects.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“The trial protocol was approved by independent ethics committees or institutional review boards at each participating site.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Trial Oversight
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In this phase 2 trial involving participants with treatment-resistant depression, psilocybin at a single dose of 25 mg, but not 10 mg, reduced depression scores significantly more than a 1-mg dose over a period of 3 weeks but was associated with adverse effects.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Rests on an assumption: The 1-mg dose of psilocybin is an inactive control that does not itself produce antidepressant effects.
- Rests on an assumption: Participants remained unaware of their trial-group assignment (dose) during the trial.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“These findings may explain the differences in efficacy between the groups in the current trial.”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Discussion
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“used remote raters who were unaware of the details of the trial and the trial-group assignments to determine the primary end-point measure (MADRS total score).”
§ Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression > Discussion
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
The paper relies on this without support.
The 1-mg dose of psilocybin is an inactive control that does not itself produce antidepressant effects.
“1 mg (control)”
The paper relies on this without support.
Participants remained unaware of their trial-group assignment (dose) during the trial.
“This was a phase 2 double-blind, dose-finding, parallel-group, randomized clinical trial.”
The paper relies on this without support.
The 1-mg dose of psilocybin is an inactive comparator that does not produce therapeutic effects.
“The change from baseline to week 3 in the MADRS total score (primary end point) was significantly better with a 25-mg dose than with a 1-mg dose; there was not significant difference between the 10-mg dose and the 1-mg dose.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source doesn’t support the claim as written.
In the citing paper
“Among outpatient participants administered psilocybin, 3 of 553 participants (0.5%) experienced worsening suicidal ideation, with 1 such episode starting on the day of dosing.28”
From Adverse Events in Studies of Classic Psychedelics: A Systematic Review and Meta-Analysis (2024) · cites this paper as [28]
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The 8% rate of severe adverse events in participants receiving psilocybin was similar to the 10% rate reported in the study by Goodwin et al in participants with TRD treated with a single 25-mg dose of psilocybin.14”
From Single-Dose Psilocybin Treatment for Major Depressive Disorder: A Randomized Clinical Trial (2023) · cites this paper as [14]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Psychedelic-assisted therapy (PAT) with psilocybin and lysergic acid diethylamide (LSD) has demonstrated efficacy in the treatment of depression, anxiety, and some other neuropsychiatric disorders”
From Naturalistic psychedelic therapy: The role of relaxation and subjective drug effects in antidepressant response (2024) · cites this paper as Goodwin et al., 2022
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Eleven of these 23 (47.8%) had treatment-resistant depression and experienced a total of 17 SAEs over 12 weeks of follow-up, including suicidal ideation (5 events), suicidal behavior (3 events), nonsuicidal intentional self-injury (4 events), adjustment disorder (2 events), worsening depression (1 event), codeine withdrawal syndrome (1 event), and hospitalization (1 event).28”
From Adverse Events in Studies of Classic Psychedelics: A Systematic Review and Meta-Analysis (2024) · cites this paper as [28]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Participants receiving the 25 mg dose, but not the 10 mg dose, exhibited a significantly greater least- squares mean change from baseline to week 3 compared with the 1 mg dose.”
From Treatment‐resistant depression: definition, prevalence, detection, management, and investigational interventions (2023) · cites this paper as [274]
The cited source says what the claim attributes to it.
In the citing paper
“The response and remission rates for the participants receiving the 25 mg dose were 37% and 29%, respectively 274 .”
From Treatment‐resistant depression: definition, prevalence, detection, management, and investigational interventions (2023) · cites this paper as [274]
The cited source says what the claim attributes to it.
In the citing paper
“Larger recent studies have addressed these issues to various degrees, but report primary end points of short duration, 14,15 leaving open the question of the long-term clinical utility of psilocybin for an often chronic condition such as MDD.”
From Single-Dose Psilocybin Treatment for Major Depressive Disorder: A Randomized Clinical Trial (2023) · cites this paper as [14]
The cited source says what the claim attributes to it.
In the citing paper
“Second, the use of niacin as active placebo may have increased believability of the comparator condition and enhanced the placebo response, given that placebo response rates in the current study were equivalent to those seen in response to a low-dose psilocybin comparator in participants with TRD and larger than the effect of an inactive placebo in a recent study in participants with MDD.14,15”
From Single-Dose Psilocybin Treatment for Major Depressive Disorder: A Randomized Clinical Trial (2023) · cites this paper as [14]
The cited source says what the claim attributes to it.
In the citing paper
“Second, the use of niacin as active placebo may have increased believability of the comparator condition and enhanced the placebo response, given that placebo response rates in the current study were equivalent to those seen in response to a low-dose psilocybin comparator in participants with TRD and larger than the effect of an inactive placebo in a recent study in participants with MDD.14,15”
From Single-Dose Psilocybin Treatment for Major Depressive Disorder: A Randomized Clinical Trial (2023) · cites this paper as [14]
The cited source says what the claim attributes to it.
In the citing paper
“Studies have used inactive placebos (e.g., [17, 35]), active placebos whose effects considerably differ from the acute effects of serotonergic psychedelics (e.g., [15, 36, 37]), or doses of psilocybin presumably too low to maintain blinding (e.g., [38, 39])”
The cited source says what the claim attributes to it.
In the citing paper
“which would theoretically not induce significant clinical benefits (e.g., [38] observed a significant decrease in depression symptomatology in participants with treatment-resistant depression after a single 25 mg dose relative to a 1 mg dose, but not with a 10 mg dose)”
The cited source says what the claim attributes to it.
In the citing paper
“Contemporary clinical studies have involved one to three dosing sessions (e.g., [38, 39, 117])”
The cited source says what the claim attributes to it.
In the citing paper
“Controlled clinical trials with psilocybin, as well as other psychedelics, have occasionally reported increases in suicidality after treatment, sometimes with extremely brief information about treatment-relatedness (Breeksema et al., 2022; Goodwin et al., 2022).”
From Naturalistic psychedelic therapy: The role of relaxation and subjective drug effects in antidepressant response (2024) · cites this paper as Goodwin et al., 2022
The cited source says what the claim attributes to it.
In the citing paper
“Research on MDD, anxiety and depressive symptoms associated with life-threatening cancer, and TRD showed the most robust evidence, supported by a non-randomized study 72 and several RCTs. 26,31-33,60,73-77”
From The revival of psilocybin between scientific excitement, evidence of efficacy, and real-world challenges (2024) · cites this paper as [75]
The cited source says what the claim attributes to it.
In the citing paper
“Blinding procedures were not consistently robust, 26,32,60,72-76 and comparison with placebo or standard treatments was lacking in many studies. 25,26,31-33,39,57,60,72,73,75-81”
From The revival of psilocybin between scientific excitement, evidence of efficacy, and real-world challenges (2024) · cites this paper as [75]
The cited source says what the claim attributes to it.
In the citing paper
“Psilocybin (4-phosphryloxy-N,N-dimethyltryptamine) is a serotonergic classic psychedelic (19–25) that has been examined in combination with psychological support as a promising treatment option in clinical trials for various disorders (26–28).”
In the citing paper
“Psychedelics such as psilocybin and lysergic acid diethylamide (LSD) are also novel therapeutics for MDD that show promise in clinical trials [124-126].”
From Beyond the serotonin deficit hypothesis: Communicating a neuroplasticity framework of major depressive disorder (2024) · cites this paper as [125]
Citations
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Self-citationTrial of Psilocybin versus Escitalopram for Depression
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Self-citationEffects of Psilocybin-Assisted Therapy on Major Depressive Disorder: A Randomized Clinical Trial
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Pilot Study of Psilocybin Treatment for Anxiety in Patients With Advanced-Stage Cancer
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McIntyre, R. S., Alsuwaidan, M., Baune, B. T., Berk, M., Demyttenaere, K., Goldberg, J. F., Gorwood, P., Ho, R., Kasper, S., Kennedy, S. H., et al. (2023) · World Psychiatry · doi:10.1002/wps.21120 · Cited by 836
Self-citationNovel and emerging treatments for major depression
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Self-citationSingle-Dose Psilocybin Treatment for Major Depressive Disorder: A Randomized Clinical Trial
Raison, C. L., Sanacora, G., Woolley, J., Heinzerling, K., Dunlop, B. W., Brown, R. T., Kakar, R., Hassman, M., Trivedi, R. P., Robison, R., et al. (2023) · JAMA · doi:10.1001/jama.2023.14530 · Cited by 545
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Psilocybin desynchronizes the human brain
Siegel, J. S., Subramanian, S., Perry, D., Kay, B. P., Gordon, E. M., Laumann, T. O., Reneau, T. R., Metcalf, N. V., Chacko, R. V., Gratton, C., et al. (2024) · Nature · doi:10.1038/s41586-024-07624-5 · Cited by 308
Self-citationHuman brain effects of DMT assessed via EEG-fMRI
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Self-citationMust Psilocybin Always “Assist Psychotherapy”?
Goodwin, G. M., Malievskaia, E., Fonzo, G. A., & Nemeroff, C. B. (2023) · American Journal of Psychiatry · doi:10.1176/appi.ajp.20221043 · Cited by 195
Self-citationExtended difficulties following the use of psychedelic drugs: A mixed methods study
Evans, J., Robinson, O. C., Argyri, E. K., Suseelan, S., Murphy-Beiner, A., McAlpine, R. G., Luke, D. P., Michelle, K., & Prideaux, E. (2023) · PLoS ONE · doi:10.1371/journal.pone.0293349 · Cited by 220
“However, McNamee et al. [12] point to evidence from trials using MDMA and psilocybin [22] showing increases of suicidal ideation and self-injury in over 7% of participants.”
Psilocybin for treatment resistant depression in patients taking a concomitant SSRI medication
Goodwin, G. M., Croal, M., Feifel, D., Kelly, J. R., Marwood, L., Mistry, S., O’Keane, V., Peck, S. K., Simmons, H., Sisa, C., et al. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-023-01648-7 · Cited by 187
“The resulting safety profile is comparable to that of psilocybin monotherapy in an open-label or controlled design [5, 47] and suggests that the safety of psilocybin in this context is Table 2.”
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Self-citationAdverse Events in Studies of Classic Psychedelics: A Systematic Review and Meta-Analysis
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Anhedonia and Depressive Disorders
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“now focusing on psilocybin, which has the further benefit of one point administration [91].”
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“A recent phase II trial 34 administering psilocybin for treatment-resistant depression funded by a pharmaceutical company registered their primary outcome on clinicaltrials. gov for the time frame ‘up to 12 weeks’, which allows for degrees of freedom in obtaining statistically significant results…”
BackgroundPsilocybin-assisted therapy for depression: A systematic review and meta-analysis
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Self-citation5-HT2ARs Mediate Therapeutic Behavioral Effects of Psychedelic Tryptamines
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Self-citationCanalization and plasticity in psychopathology
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Self-citationAcute Adverse Effects of Therapeutic Doses of Psilocybin
Yerubandi, A., Thomas, J. E., Bhuiya, N. M. M. A., Harrington, C. A., Zapata, L. V., & Caballero, J. (2024) · JAMA Network Open · doi:10.1001/jamanetworkopen.2024.5960 · Cited by 111
Beyond the 5-HT2AReceptor: Classic and Nonclassic Targets in Psychedelic Drug Action
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Psilocybin’s lasting action requires pyramidal cell types and 5-HT2A receptors
Shao, L.-X., Liao, C., Davoudian, P. A., Savalia, N. K., Jiang, Q., Wojtasiewicz, C., Tan, D., Nothnagel, J. D., Liu, R., Woodburn, S. C., et al. (2025) · Nature · doi:10.1038/s41586-025-08813-6 · Cited by 115
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“These findings suggest psilocybin may have a time-limited window of antidepressant effects, consistent with clinical trial data (14, 15, 61), and imply that some individuals may require repeated psilocybin dosing for continued antidepressant benefits.”
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Efficacy of psilocybin for treating symptoms of depression: systematic review and meta-analysis
Metaxa, A.-M., & Clarke, M. J. (2024) · BMJ · doi:10.1136/bmj-2023-078084 · Cited by 107
“Although some studies used low dose psychedelics as comparators to deal with this problem (eg, Carhart-Harris et al, 63 Goodwin et al, 18 Griffiths et al 14 ) or used a niacin placebo that can induce effects similar to those of psilocybin (eg, Grob et al, 15 Ross et al 17 ), the extent to which…”
BackgroundMethodInfluentialCardiac Roles of Serotonin (5-HT) and 5-HT-Receptors in Health and Disease
Neumann, J., Hofmann, B., Dhein, S., & Gergs, U. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054765 · Cited by 83
Schneier, F. R., Feusner, J., Wheaton, M. G., Gomez, G. J., Cornejo, G., Naraindas, A. M., & Hellerstein, D. J. (2023) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2023.03.031 · Cited by 81
Self-citationSekssaoui, M., Bockaert, J., Marin, P., & Bécamel, C. (2024) · Neuropsychopharmacology · doi:10.1038/s41386-024-01794-6 · Cited by 84
Structural pharmacology and therapeutic potential of 5-methoxytryptamines
Warren, A. L., Lankri, D., Cunningham, M. J., Serrano, I. C., Parise, L. F., Kruegel, A. C., Duggan, P., Zilberg, G., Capper, M. J., Havel, V., et al. (2024) · Nature · doi:10.1038/s41586-024-07403-2 · Cited by 84
The Psychedelic Future of Post-Traumatic Stress Disorder Treatment
Zaretsky, T. G., Jagodnik, K. M., Barsic, R., Antonio, J. H., Bonanno, P. A., MacLeod, C., Pierce, C., Carney, H., Morrison, M. T., Saylor, C. F., et al. (2024) · Current Neuropharmacology · doi:10.2174/1570159x22666231027111147 · Cited by 92
Levin, A. W., Lancelotta, R., Sepeda, N. D., Gukasyan, N., Nayak, S., Wagener, T. L., Barrett, F. S., Griffiths, R. R., & Davis, A. K. (2024) · PLoS ONE · doi:10.1371/journal.pone.0300501 · Cited by 82
Magnesium–ibogaine therapy in veterans with traumatic brain injuries
Cherian, K. N., Keynan, J. N., Anker, L. A., Faerman, A., Brown, R. E., Shamma, A., Keynan, O., Coetzee, J. P., Batail, J.-M. V., Phillips, A., et al. (2024) · Nature Medicine · doi:10.1038/s41591-023-02705-w · Cited by 80
“Similarly, psilocybin has demonstrated improvements in depression, substance use and anxiety 60–63 .”
Therapeutic mechanisms of psychedelics and entactogens
Heifets, B. D., & Olson, D. E. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-023-01666-5 · Cited by 70
“For classical psychedelics, the most well-powered clinical studies have dealt with major depressive disorder [3, 6, 8, 83] and alcohol use disorder [84, 207].”
BackgroundInfluentialKrystal, J. H., Kaye, A. P., Jefferson, S., Girgenti, M. J., Wilkinson, S. T., Sanacora, G., & Esterlis, I. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2305772120 · Cited by 83
“It is not clear whether this dif - ference contributes to the long - lasting antidepressant effects of psychedelics (151).”
BackgroundDuan, W., Cao, D., Wang, S., & Cheng, J. (2023) · Chemical Reviews · doi:10.1021/acs.chemrev.3c00375 · Cited by 81
Structural neural plasticity evoked by rapid-acting antidepressant interventions
Liao, C., Dua, A. N., Wojtasiewicz, C., Liston, C. M., & Kwan, A. C. (2024) · Nature reviews. Neuroscience · doi:10.1038/s41583-024-00876-0 · Cited by 81
“All profiles are schematic but based on data from published studies (ketamine spine formation and density timing 5,8 , ketamine therapeutic onset 20 , psilocybin spine formation and density timing 9 , psilocybin ther apeutic onset 86 and TMS therapeutic onset 22 ). rTMS, repetitive TMS.”
Johnston, J. N., Kadriu, B., Allen, J., Gilbert, J. R., Henter, I. D., & Zarate, C. A. (2023) · Neuropharmacology · doi:10.1016/j.neuropharm.2023.109422 · Cited by 73
Fungal Drug Discovery for Chronic Disease: History, New Discoveries and New Approaches
Prescott, T. A. K., Hill, R., Mas‐Claret, E., Gaya, E., & Burns, E. (2023) · Biomolecules · doi:10.3390/biom13060986 · Cited by 68
“A 2021 study examining the effects of psilocybin on major depressive disorder found psilocybin to be effective, with 13 participants (54%) all in remission at week 4 [63].”
BackgroundAttenuation of psilocybin mushroom effects during and after SSRI/SNRI antidepressant use
Gukasyan, N., Griffiths, R. R., Yaden, D. B., Antoine, D. G., & Nayak, S. M. (2023) · Journal of Psychopharmacology · doi:10.1177/02698811231179910 · Cited by 67
Chen, Y., Guo, Y., Wu, H., Tang, Y.-J., Sooranna, S. R., Zhang, L., Chen, T., Xie, X., Qiu, L., & Wu, X. (2024) · JAMA Network Open · doi:10.1001/jamanetworkopen.2024.0953 · Cited by 66
Psychedelic Commercialization: A Wide-Spanning Overview of the Emerging Psychedelic Industry
Aday, J. S., Barnett, B. S., Grossman, D., Murnane, K. S., Nichols, C. D., & Hendricks, P. S. (2023) · Psychedelic Medicine · doi:10.1089/psymed.2023.0013 · Cited by 65
“…rate at 3 weeks as opposed to 67% and 42% at 1 week and 3 months, respectively, seen in a previous smaller open-label trial of psilocybin-assisted psycho-therapy for TRD. 63,64 ), as well as safety concerns prompted by a small number of participants reporting suicidal behavior post-treatment.”
Clinically relevant acute subjective effects of psychedelics beyond mystical experience
Yaden, D. B., Goldy, S. P., Weiss, B., & Griffiths, R. R. (2024) · Nature Reviews Psychology · doi:10.1038/s44159-024-00345-6 · Cited by 67
Page, C. E., Epperson, C. N., Novick, A. M., Duffy, K. A., & Thompson, S. M. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02625-2 · Cited by 80
Kopra, E. I., Ferris, J., WINSTOCK, A. R., Kuypers, K. P. C., Young, A. H., & Rucker, J. (2023) · Journal of Psychopharmacology · doi:10.1177/02698811231158245 · Cited by 67
Self-citationZeifman, R. J., Wagner, A. C., Monson, C. M., & Carhart-Harris, R. L. (2023) · Journal of Affective Disorders · doi:10.1016/j.jad.2023.04.105 · Cited by 68
Self-citationThe polypharmacology of psychedelics reveals multiple targets for potential therapeutics
Jain, M. K., Gumpper, R. H., Slocum, S. T., Schmitz, G. P., Madsen, J. S., Tummino, T. A., Suomivuori, C., Huang, X.-P., Shub, L., DiBerto, J. F., et al. (2025) · Neuron · doi:10.1016/j.neuron.2025.06.012 · Cited by 74
Psychiatric risks for worsened mental health after psychedelic use
Marrocu, A., Kettner, H., Weiss, B., Zeifman, R. J., Erritzoe, D., & Carhart-Harris, R. L. (2024) · Journal of Psychopharmacology · doi:10.1177/02698811241232548 · Cited by 60
“Thus, the brief (e.g., one dose, minimal aftercare) psychedelic therapy package being trialed for treatment-resistant depression (Goodwin et al., 2022) may not be sufficiently safe for cases where there is a diagnosed or suspected BPD.”
BackgroundSelf-citationSloshower, J., Zeifman, R. J., Guss, J., Krause, R., Safi-Aghdam, H., Pathania, S., Pittman, B., & D’Souza, D. C. (2024) · Scientific Reports · doi:10.1038/s41598-024-58318-x · Cited by 65
Cardiovascular safety of psychedelic medicine: current status and future directions
Wsół, A. (2023) · Pharmacological Reports · doi:10.1007/s43440-023-00539-4 · Cited by 71
“A more serious adverse effect after psilocybin administration was a prolongation of the QTc interval [120].”
BackgroundBreeksema, J. J., Niemeijer, A., Krediet, E., Karsten, T., Kamphuis, J., Vermetten, E., van den Brink, W., & Schoevers, R. (2024) · Scientific Reports · doi:10.1038/s41598-024-53188-9 · Cited by 58
“Further details of the study are published elsewhere 8 .”
BackgroundSelf-citationAustralia to prescribe MDMA and psilocybin for PTSD and depression in world first
Haridy, R. (2023) · Nature · doi:10.1038/d41586-023-02093-8 · Cited by 57
Rieser, N. M., Bitar, R., Halm, S., Rossgoderer, C., Gubser, L. P., Thévenaz, M., Kreis, Y., von Rotz, R., Nordt, C., Visentini, M., et al. (2025) · EClinicalMedicine · doi:10.1016/j.eclinm.2025.103149 · Cited by 63
“Second, in line with previously reported increased quality of life in depression and anxiety patients following psilocybin-assisted therapy, 28,29 we found improved quality of life post psilocybin administration in AUD patients.”
Mechanisms and molecular targets surrounding the potential therapeutic effects of psychedelics
Jaster, A. M., & González‐Maeso, J. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02274-x · Cited by 56
“…being tested as a treatment for several psychiatric conditions including major depression [199 – 201] and treatment-resistant depression [23, 202, 203], generalized [204] and end-of-life anxiety [22, 205], post-traumatic stress disorder [206], smoking cessation [207, 208], and alcohol use…”
Risk of bias in randomized clinical trials on psychedelic medicine: A systematic review
Hovmand, O. R., Poulsen, E. D., Arnfred, S., & Storebø, O. J. (2023) · Journal of Psychopharmacology · doi:10.1177/02698811231180276 · Cited by 63
Safety and risk assessment of psychedelic psychotherapy: A meta-analysis and systematic review
Roméo, B., Kervadec, E., Fauvel, B., Strika-Bruneau, L., Amirouche, A., Verroust, V., Piolino, P., & Benyamina, A. (2024) · Psychiatry Research · doi:10.1016/j.psychres.2024.115880 · Cited by 69
Arnsten, A. F. T., Joyce, M. K. P., & Roberts, A. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.105000 · Cited by 64
“, 2021), including a recent, large Phase 2 study (Goodwin et al., 2022).”
Holze, F., Singh, N., Liechti, M. E., & D’Souza, D. C. (2024) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2024.01.007 · Cited by 62
Erritzøe, D., Barba, T., Greenway, K. T., Murphy, R., Martell, J., Giribaldi, B., Timmermann, C., Murphy-Beiner, A., Baker-Jones, M., Nutt, D., et al. (2024) · EClinicalMedicine · doi:10.1016/j.eclinm.2024.102799 · Cited by 68
“Phase 1, 17 Phase 2A 5,18 and Phase 2B 19,20 trials have demonstrated that one or two doses of psilocybin, administered with psychological support, can produce almost immediate reductions in depressive symptoms that may persist for months.”
Self-citationPsychedelics as Transformative Therapeutics
Roth, B. L., & Gumpper, R. H. (2023) · American Journal of Psychiatry · doi:10.1176/appi.ajp.20230172 · Cited by 57
Essentials of Informed Consent to Psychedelic Medicine
Marks, M., Brendel, R. W., Shachar, C., & Cohen, I. G. (2024) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2024.0184 · Cited by 56
Sabé, M., Sulstarova, A., Glangetas, A., Pieri, M. D., Mallet, L., Curtis, L., Richard-Lepouriel, H., Penzenstadler, L. E., Seragnoli, F., Thorens, G., et al. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02800-5 · Cited by 61
Chen, T., Cheng, L., Ma, J., Yuan, J., Pi, C., Xiong, L., Chen, J., Liu, H., Tang, J., Zhong, Y., et al. (2023) · Pharmacological Research · doi:10.1016/j.phrs.2023.106837 · Cited by 59
Noorani, T. N., Bedi, G., & Muthukumaraswamy, S. D. (2023) · Psychological Medicine · doi:10.1017/s0033291723001289 · Cited by 64
Hashimoto, K. (2024) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-024-01770-7 · Cited by 58
New and emerging treatments for major depressive disorder
Njenga, C., Ramanuj, P., de Magalhães, F. J. C., & Pincus, H. A. (2024) · BMJ · doi:10.1136/bmj-2022-073823 · Cited by 51
“24 25 Challenging intense emotions such as fear, anxiety, and sadness—a common side effect of psychedelic therapy, especially in the acute phase—are widely hypothesized to be an important part of the therapeutic experience, often as part of an “emotional breakthrough.””
BackgroundInfluentialPsychedelic therapies reconsidered: compounds, clinical indications, and cautious optimism
Mitchell, J., & Anderson, B. T. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-023-01656-7 · Cited by 55
“Similarly, a recent phase 2 trial of psilocybin therapy for an episode of treatment-resistant depression showed that, while 37% of participants displayed a clinically meaningful response to psilocy-bin at the primary endpoint (week 3), most did not [56].”
BackgroundKiilerich, K. F., Lorenz, J., Scharff, M. B., Speth, N., Brandt, T. G., Czurylo, J., Xiong, M., Jessen, N. S., Casado-Sainz, A., Shalgunov, V., et al. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02280-z · Cited by 48
“The serotonergic psychedelic prodrug psilocybin ([3-(2-dimethy-laminoethyl)-1H-indol-4-yl] dihydrogen phosphate) has received increasing attention in recent years for the treatment of depression, end-of-life anxiety, and substance use disorders.”
InfluentialEliminating Ambiguous Treatment Effects Using Estimands
Kahan, B. C., Cro, S., Li, F., & Harhay, M. O. (2023) · American Journal of Epidemiology · doi:10.1093/aje/kwad036 · Cited by 50
“Furthermore, some published trial reports and protocols have begun using estimands to clarify reported treatment effects (34–37).”
Brennan, B., Kelman, A. R., & Belser, A. (2023) · Psychedelic Medicine · doi:10.1089/psymed.2023.0007 · Cited by 50
Psychedelic-assisted psychotherapy: Where is the psychotherapy research
Aday, J. S., Horton, D., Fernandes-Osterhold, G., O’Donovan, A., Bradley, E. R., Rosen, R. C., & Woolley, J. D. (2024) · Psychopharmacology · doi:10.1007/s00213-024-06620-x · Cited by 54
“Yet, the same researchers expressing skepticism of the necessity of psychotherapy in PAP recently published a phase 2 clinical trial (Goodwin et al. 2022) that included (a) trained “therapists” present at each stage of the study intervention, (b) an unpub-lished “therapist manual” guiding therapist…”
The Bright Side of Psychedelics: Latest Advances and Challenges in Neuropharmacology
Mastinu, A., Anyanwu, M., Carone, M., Abate, G., Bonini, S. A., Peron, G., Tirelli, E., Pucci, M., Ribaudo, G., Oselladore, E., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021329 · Cited by 52
The need for establishing best practices and gold standards in psychedelic medicine
Feduccia, A. A., Agin-Liebes, G., Price, C. M., Grinsell, N., Paradise, S., & Rabin, D. M. (2023) · Journal of Affective Disorders · doi:10.1016/j.jad.2023.03.083 · Cited by 44
Ethnoracial inclusion in clinical trials of psychedelics: a systematic review
Hughes, M. E., & Garcia‐Romeu, A. (2024) · EClinicalMedicine · doi:10.1016/j.eclinm.2024.102711 · Cited by 49
“8 However, the present review indicates an ongoing diversity problem in psychedelic clinical trials.”
BackgroundFalchi-Carvalho, M., Palhano-Fontes, F., Wießner, I., Barros, H., Bolcont, R., Laborde, S., Silva, S. R. B., Montanini, D., Barbosa, D. C., Teixeira, E., et al. (2025) · Neuropsychopharmacology · doi:10.1038/s41386-025-02091-6 · Cited by 52
Rijsketic, D. R., Casey, A. B., Barbosa, D. A. N., Zhang, X., Hietamies, T. M., Ramirez-Ovalle, G., Pomrenze, M. B., Halpern, C. H., Williams, L. M., Malenka, R. C., et al. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-023-01613-4 · Cited by 46
“INTRODUCTION The therapeutic potential of serotonergic psychedelics like psilocybin is promising [1], but factors contributing to their efficacy are poorly understood.”
BackgroundThe role of the psychedelic experience in psilocybin treatment for treatment-resistant depression
Goodwin, G. M., Aaronson, S. T., Alvarez, O., Carhart-Harris, R. L., Chai-Rees, J., Croal, M., DeBattista, C., Dunlop, B. W., Feifel, D., Hellerstein, D. J., et al. (2024) · Journal of Affective Disorders · doi:10.1016/j.jad.2024.12.061 · Cited by 52
Self-citationRoméo, B., Kervadec, E., Fauvel, B., Strika-Bruneau, L., Amirouche, A., Bezo, A., Piolino, P., & Benyamina, A. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106086 · Cited by 53
The costs and benefits of psychedelics on cognition and mood
Sayalı, C., & Barrett, F. S. (2023) · Neuron · doi:10.1016/j.neuron.2022.12.031 · Cited by 47
Back, A. L., Freeman-Young, T. K., Morgan, L., Sethi, T., Baker, K. K., Myers, S., McGregor, B. A., Harvey, K., Tai, M., Kollefrath, A. W., et al. (2024) · JAMA Network Open · doi:10.1001/jamanetworkopen.2024.49026 · Cited by 52
Honk, L., Stenfors, C. U. D., Goldberg, S. B., Hendricks, P. S., Osika, W., Dourron, H. M., Lebedev, A. V., Petrović, P., & Simonsson, O. (2024) · Journal of Affective Disorders · doi:10.1016/j.jad.2024.01.197 · Cited by 48
Psilocybin Facilitates Fear Extinction: Importance of Dose, Context, and Serotonin Receptors
Woodburn, S. C., Levitt, C. M., Koester, A., & Kwan, A. C. (2024) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.4c00279 · Cited by 49
Discovering the Potential Mechanisms of Medicinal Mushrooms Antidepressant Activity: A Review
Lazur, J., Hnatyk, K., Kała, K., Sułkowska‐Ziaja, K., & Muszyńska, B. (2023) · Antioxidants · doi:10.3390/antiox12030623 · Cited by 44
“Although there is no definitive verdict on the use of psychedelics in the treatment of Major Depressive Disorder, based on randomized clinical trials conducted with psilocybin, shortand long-term reductions in depressive symptoms have been observed [83].”
BackgroundVilliger, D., & Trachsel, M. (2023) · Journal of Medical Ethics · doi:10.1136/jme-2022-108816 · Cited by 43
Husain, M. I., Blumberger, D. M., Castle, D. J., Ledwos, N., Fellows, E., Jones, B. D. M., Ortiz, A., Kloiber, S. M., Wang, W., Rosenblat, J. D., et al. (2023) · BJPsych Open · doi:10.1192/bjo.2023.535 · Cited by 48
“14 Does psilocybin require psychedelic effects to treat depression?”
Self-citationIsolation of psychedelic-responsive neurons underlying anxiolytic behavioral states
Muir, J., Lin, S., Aarrestad, I. K., Daniels, H. R., Ma, J., Tian, L., Olson, D. E., & Kim, C. K. (2024) · Science · doi:10.1126/science.adl0666 · Cited by 49
The effect of lysergic acid diethylamide (LSD) on whole-brain functional and effective connectivity
Bedford, P., Hauke, D. J., Wang, Z., Röth, V., Nagy-Huber, M., Holze, F., Ley, L., Vizeli, P., Liechti, M. E., Borgwardt, S., et al. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-023-01574-8 · Cited by 42
“INTRODUCTION Psychedelics like psilocybin and lysergic acid diethylamide (LSD) have emerged as promising new treatment candidates for a variety of psychiatric conditions including substance dependence [1–3], major depression [4], anxiety disorders [5], and adjustment disorders [6–8].”
BackgroundEffects of DMT on mental health outcomes in healthy volunteers
Timmermann, C., Zeifman, R. J., Erritzøe, D., Nutt, D., & Carhart-Harris, R. L. (2024) · Scientific Reports · doi:10.1038/s41598-024-53363-y · Cited by 48
“This may be especially relevant for patients who experience a recurrence of their clinical symptoms following psilocybin therapy (see 5,8 for examples) and may benefit from shorter (e.g., pro re nata) interventions as treatment follow-ups.”
BackgroundSelf-citationMcCrone, P., Fisher, H., Knight, C., Harding, R., Schlag, A. K., Nutt, D. J., & Neill, J. C. (2023) · Psychological Medicine · doi:10.1017/s0033291723001411 · Cited by 42
Qu, Y., Chang, L., Ma, L., Wan, X., & Hashimoto, K. (2022) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2022.173500 · Cited by 44
Greater subjective effects of a low dose of LSD in participants with depressed mood
Molla, H. M., Lee, R., Tare, I., & de Wit, H. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-023-01772-4 · Cited by 44
“One promising new candidate treatment is administration of single high doses of psychedelic compounds such as psilocybin and lysergic acid diethylamide (LSD), combined with supportive psychotherapy [3 – 7].”
Rucker, J., Roberts, C., Seynaeve, M., Young, A. H., Suttle, B., Yamamoto, T., Ermakova, A. O., Dunbar, F., & Wiegand, F. (2024) · Journal of Psychopharmacology · doi:10.1177/02698811241246857 · Cited by 47
“Several psychedelic compounds are undergoing clinical trials to assess their utility for various neuropsychiatric indications, and some have shown encouraging efficacy signals in larger controlled clinical trials (Goodwin et al., 2022).”
BackgroundSelf-citationPsilocybin in Treatment-Resistant Depression
Madras, B. K. (2022) · New England Journal of Medicine · doi:10.1056/nejme2210975 · Cited by 41
Personality change in a trial of psilocybin therapy v. escitalopram treatment for depression
Weiss, B., Ginige, I., Shannon, L., Giribaldi, B., Murphy-Beiner, A., Murphy, R., Baker-Jones, M., Martell, J., Nutt, D. J., Carhart-Harris, R. L., et al. (2023) · Psychological Medicine · doi:10.1017/s0033291723001514 · Cited by 48
“…psychedelic therapy has been increasingly studied as a psychiatric intervention, with ten published clinical trials demonstrating promising efficacy for depressive symptoms (e.g. Carhart-Harris et al., 2016a; Davis et al., 2021; Goodwin et al., 2022; Ross et al., 2016; Sloshower et al., 2023).”
Self-citationLSD-assisted therapy in patients with anxiety: open-label prospective 12-month follow-up
Holze, F., Gasser, P., Müller, F., Strebel, M., & Liechti, M. E. (2024) · The British Journal of Psychiatry · doi:10.1192/bjp.2024.99 · Cited by 46
“4,8,9 The primary analysis of the present crossover trial, including the primary end-point at 16 weeks post-LSD treatment compared with placebo, showed significant, rapid and sustained reductions of anxiety and comorbid depression in people with anxiety disorders with or without life-threatening…”
BackgroundSingle Treatment With MM120 (Lysergide) in Generalized Anxiety Disorder
Robison, R. J., Barrow, R., Conant, C., Foster, E., Freedman, J. M., Jacobsen, P. L., Jemison, J., Karas, S. M., Karlin, D. R., Solomon, T. M., et al. (2025) · JAMA · doi:10.1001/jama.2025.13481 · Cited by 44
Assessment of the Acute Effects of 2C‐B vs. Psilocybin on Subjective Experience, Mood, and Cognition
Mallaroni, P., Mason, N. L., Reckweg, J. T., Paci, R., Ritscher, S., Toennes, S. W., Theunissen, E. L., Kuypers, K. P. C., & Ramaekers, J. G. (2023) · Clinical Pharmacology & Therapeutics · doi:10.1002/cpt.2958 · Cited by 42
Metadata
- Authors
- Goodwin, G. M., Aaronson, S. T., Alvarez, O., Arden, P. C., Baker, A., Bennett, J. C., Bird, C., Blom, R. E., Brennan, C., Brusch, D., Burke, L., Campbell-Coker, K., Carhart-Harris, R., Cattell, J., Daniel, A., DeBattista, C., Dunlop, B. W., Eisen, K., Feifel, D., Forbes, M., Haumann, H. M., Hellerstein, D. J., Hoppe, A. I., Husain, M. I., Jelen, L. A., Kamphuis, J., Kawasaki, J., Kelly, J. R., Key, R. E., Kishon, R., Knatz Peck, S., Knight, G., Koolen, M. H. B., Lean, M., Licht, R. W., Maples-Keller, J. L., Mars, J., Marwood, L., McElhiney, M. C., Miller, T. L., Mirow, A., Mistry, S., Mletzko-Crowe, T., Modlin, L. N., Nielsen, R. E., Nielson, E. M., Offerhaus, S. R., O’Keane, V., Páleníček, T., Printz, D., Rademaker, M. C., van Reemst, A., Reinholdt, F., Repantis, D., Rucker, J., Rudow, S., Ruffell, S., Rush, A. J., Schoevers, R. A., Seynaeve, M., Shao, S., Soares, J. C., Somers, M., Stansfield, S. C., Sterling, D., Strockis, A., Tsai, J., Visser, L., Wahba, M., Williams, S., Young, A. H., Ywema, P., Zisook, S., & Malievskaia, E.
- Affiliations
- King's College London (GB)
- SUNY Downstate Health Sciences University (US)
- From COMPASS Pathfinder (G.M.G., J.C.B., L.M., S.M., S.C.S., J.T., S.W., E.M.), the Department of Psychological Medicine, Institute of Psychiatry, Psychology, and Neuroscience, King’s College London (C. Bird, L.A.J., G.K., L.N.M., F.R., J.R., S. Ruffell, M. Seynaeve, A.H.Y.), the National Institute for Health and Care Research Clinical Research Facility, King’s College Hospital NHS Foundation Trust (K.C.-C., J.C., A.D.), and South London and Maudsley NHS Foundation Trust, Bethlem Royal Hospital (L.A.J., L.N.M., J.R., A.H.Y.), London, and the Cumbria, Northumberland, Tyne and Wear Foundation Trust and Newcastle University, Newcastle (M.W.) — all in the United Kingdom; the Institute for Advanced Diagnostics and Therapeutics, Sheppard Pratt, Baltimore (S.T.A., M.F., T.L.M., S. Rudow); Sant Joan de Déu Hospital and the Sant Joan de Déu Research Foundation, Barcelona (O.A.); SUNY Downstate College of Medicine (P.C.A.), the New York State Psychiatric Institute (D.J.H., R.E.K., R.K., M.C.M., E.M.N.), and the Depa...
- University of California, San Francisco (US)
- Emory University (US)
- University Medical Center Groningen (NL)
- Duke University (US)
- ORCID
- Goodwin, Guy M.
- Aaronson, Scott T.
- Bird, Catherine
- Burke, Lisa
- Carhart-Harris, Robin
- Daniel, Aster
- DeBattista, Charles
- Dunlop, Boadie W.
- Eisen, Katherine
- Feifel, David
- Hellerstein, David J.
- Husain, Muhammad I.
- Jelen, Luke A.
- Kamphuis, Jeanine
- Kawasaki, Julie
- Kelly, John R.
- Kishon, Ronit
- Knight, Gemma
- Lean, Melanie
- Licht, Rasmus W.
- Marwood, Lindsey
- McElhiney, Martin C.
- Nielsen, René E.
- Nielson, Elizabeth M.
- O’Keane, Veronica
- Páleníček, Tomáš
- Repantis, Dimitris
- Rucker, James
- Ruffell, Simon
- Rush, A. John
- Schoevers, Robert A.
- Seynaeve, Mathieu
- Soares, Jair C.
- Somers, Metten
- Wahba, Mourad
- Williams, Samuel
- Young, Allan H.
- Zisook, Sidney
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 2022-11-03
- Volume
- 387
- Issue
- 18
- Pages
- 1637-1648
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W4308146982
- Cited by
- 1,167
- References
- 19
- Citations by year
- 2026: 275 · 2025: 327 · 2024: 333 · 2023: 216 · 2022: 15
- FWCI
- 203.26
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- New England Journal of Medicine (publishedVersion)
- PubMed (publishedVersion)
- Research Portal (King's College London) (submittedVersion, other-oa)
- VBN Forskningsportal (Aalborg Universitet) (submittedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion, other-oa)
- Newcastle University ePrints (Newcastle Univesity)
- Funders
- COMPASS Pathfinder Limited
- Topics
- Social Sciences › Psychology › Clinical Psychology › Psychedelics and Drug Studies
- Health Sciences › Medicine › Pharmacology (medical) › Treatment of Major Depression
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Keywords
- psilocybin, treatment-resistant depression, major depressive episode, single-dose administration, dose-response relationship, antidepressant efficacy, adverse events, suicidal ideation, psychedelic therapy
- MeSH terms
- Adult, Antidepressive Agents, Depression, Major Depressive Disorder, Double-Blind Method, Humans, Psilocybin, Treatment Outcome, Depressive Disorder, Treatment-Resistant
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
A language model drew the claims from the paper on 2026-10-11, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).
A second model labelled each claim on 2026-10-11 (model jev-1.13-20260917, definition revision gold-guideline-v0.2).
Cited sources are checked with a language model’s help (gpt-6-sol).
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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