Cited by 11Alzheimer's disease research and treatmentsDementia and Cognitive Impairment ResearchAmyotrophic Lateral Sclerosis Research

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Exploratory analyses of clinical outcomes from the BIIB080 phase 1b study in mild Alzheimer’s disease

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Abstract

This study conducted exploratory analyses of the effects of BIIB080, a MAPT (microtubule-associated protein tau)-targeting antisense oligonucleotide, in participants with mild Alzheimer’s disease. A multicenter, randomized, double-blind, phase 1b trial was conducted as a placebo-controlled, multiple-ascending dose (MAD) study followed by an open-label, long-term extension (LTE). During the MAD study, participants were randomized and received either intrathecal placebo or BIIB080 10 mg (n = 6), 30 mg (n = 6) or 60 mg (n = 9) every 4 weeks or 115 mg (n = 13) every 12 weeks (Q12W). During the LTE, participants received high-dose BIIB080 (60 mg (n = 7) or 115 mg (n = 9) Q12W). BIIB080 was generally well tolerated. Here we present findings from exploratory analyses, which showed a consistent trend of slowed decline on cognitive, functional and global measures favoring BIIB080 high-dose groups at the end of both study periods. This favorable trend is supported by reported reductions from baseline in brain neurofibrillary tangles measured with tau positron emission tomography. Trial registration: ClinicalTrials.gov identifier: NCT03186989 . This exploratory analysis of a phase 1b study evaluating BIIB080, a MAPT-targeting antisense oligonucleotide, in mild Alzheimer’s disease indicates favorable trends of high-dose BIIB080 in slowing cognitive and functional decline, supporting the need for future trials evaluating clinical efficacy of BIIB080 in mild Alzheimer’s disease.

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  1. Coomans, E. M. et al. A head-to-head comparison between plasma ptau181 and tau PET along the Alzheimer’s disease continuum. J. Nucl. Med. 64, 437–443 (2023). · DOI
  2. Mummery, C. J. et al. Tau-targeting antisense oligonucleotide MAPTRX in mild Alzheimer’s disease: a phase 1b, randomized, placebo-controlled trial. Nat. Med. 29, 1437–1447 (2023). · DOI · Paper page
  3. Budd Haeberlein, S. et al. Two randomized phase 3 studies of aducanumab in early Alzheimer’s disease. J. Prev. Alzheimers Dis. 9, 197–210 (2022). · DOI · Paper page
  4. Sims, J. R. et al. Donanemab in early symptomatic Alzheimer disease: the TRAILBLAZER-ALZ 2 randomized clinical trial. JAMA 330, 512–527 (2023). · DOI · Paper page
  5. Corsi, A. et al. Tau isoforms: gaining insight into MAPT alternative splicing. Int. J. Mol. Sci. 23, 15383 (2022). · DOI
  6. Yang, J. et al. Complicated role of post-translational modification and protease-cleaved fragments of tau in Alzheimer’s disease and other tauopathies. Mol. Neurobiol. 61, 4712–4731 (2024). · DOI
  7. Malpetti, M., Joie, R. & Rabinovici, G. D. Tau beats amyloid in predicting brain atrophy in Alzheimer disease: implications for prognosis and clinical trials. J. Nucl. Med. 63, 830–832 (2022). · DOI · Paper page
  8. van Dyck, C. H. et al. Lecanemab in early Alzheimer’s disease. N. Engl. J. Med. 388, 9–21 (2023). · DOI · Paper page
  9. Austin, P. C. An introduction to propensity score methods for reducing the effects of confounding in observational studies. Multivar. Behav. Res. 46, 399–424 (2011). · DOI · Paper page
  10. O’Bryant, S. E. et al. Staging dementia using Clinical Dementia Rating Scale Sum of Boxes scores: a Texas Alzheimer’s Research Consortium study. Arch. Neurol. 65, 1091–1095 (2008). · DOI
  11. DeVos, S. L. et al. Antisense reduction of tau in adult mice protects against seizures. J. Neurosci. 33, 12887–12897 (2013). · DOI · Paper page
  12. Albert, M. S. et al. The diagnosis of mild cognitive impairment due to Alzheimer’s disease: recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease. Alzheimers Dement 7, 270–279 (2011). · DOI · Paper page
  13. Folstein, M. F., Folstein, S. E. & McHugh, P. R. ‘Mini-mental state’. A practical method for grading the cognitive state of patients for the clinician. J. Psychiatr. Res. 12, 189–198 (1975). · DOI · Paper page
  14. Kennedy, R. E. et al. Using baseline cognitive severity for enriching Alzheimer’s disease clinical trials: how does Mini-Mental State Examination predict rate of change? Alzheimers Dement. (N Y) 1, 46–52 (2015). · DOI
  15. Morris, J. C. The Clinical Dementia Rating (CDR): current version and scoring rules. Neurology 43, 2412–2414 (1993). · DOI · Paper page
  16. Marshall, G. A. et al. Executive function and instrumental activities of daily living in mild cognitive impairment and Alzheimer’s disease. Alzheimers Dement. 7, 300–308 (2011). · DOI
  17. Brown, P. J. et al. Functional impairment in elderly patients with mild cognitive impairment and mild Alzheimer disease. Arch. Gen. Psychiatry 68, 617–626 (2011). · DOI · Paper page
  18. Pfeffer, R. I. et al. Measurement of functional activities in older adults in the community. J. Gerontol. 37, 323–329 (1982). · DOI
  19. Randolph, C. et al. The Repeatable Battery for the Assessment of Neuropsychological Status (RBANS): preliminary clinical validity. J. Clin. Exp. Neuropsychol. 20, 310–319 (1998). · DOI · Paper page
  20. Duff, K. et al. Diagnostic accuracy of the RBANS in mild cognitive impairment: limitations on assessing milder impairments. Arch. Clin. Neuropsychol. 25, 429–441 (2010). · DOI
  21. Randolph, C. RBANS: Repeatable Battery for the Assessment of Neuropsychological Status: Manual (The Psychological Corporation, 1998). · DOI
  22. Shulman, M. et al. TANGO: a placebo-controlled randomized phase 2 study of efficacy and safety of the anti-tau monoclonal antibody gosuranemab in early Alzheimer’s disease. Nat. Aging 3, 1591–1601 (2023). · DOI

Metadata

Authors
Shulman, M., Wu, S., Ziogas, N., Edwards, A., Collins, J., Lin, L., Tien, I., Curiale, G., Li, Y., Mummery, C., Lane, R., Junge, C., Beaver, J., Tian, Y., Landen, J., Bullain, S., & Gallagher, D.
Affiliations
  • Biogen (United States) (US)
  • National Hospital for Neurology and Neurosurgery (GB)
  • Ionis Pharmaceuticals (United States) (US)
Corresponding author
Shulman, Melanie
Venue
Nature Aging
Published
2026-02-11
Volume
6
Issue
2
Pages
445-453
ISSN
2662-8465 (ISSN-L)
OpenAlex
W7128599889
Cited by
11
References
5
Citations by year
2026: 11
FWCI
40.86
Type
journal article
Language
en
Open access
Locations
  • Nature Aging (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • PubMed Central (publishedVersion, cc-by-nc-nd)
Funders
Ionis and Biogen Inc.
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Clinical Neurology › Amyotrophic Lateral Sclerosis Research
Keywords
MAPT, mild Alzheimer's disease, intrathecal drug delivery, cognitive decline, functional decline, neurofibrillary tangles, tau PET, dose escalation, long-term extension study
MeSH terms
Aged, Aged, 80 and over, Alzheimer Disease, Cognition, Dose-Response Relationship, Drug, Double-Blind Method, Female, Humans, Indoles, Male, Oligonucleotides, Oligonucleotides, Antisense, tau Proteins, Treatment Outcome

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