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A Phase 3 Randomized Trial of Voxelotor in Sickle Cell Disease
Open accessAbstract
BACKGROUND: Deoxygenated sickle hemoglobin (HbS) polymerization drives the pathophysiology of sickle cell disease. Therefore, direct inhibition of HbS polymerization has potential to favorably modify disease outcomes. Voxelotor is an HbS polymerization inhibitor. METHODS: In a multicenter, phase 3, double-blind, randomized, placebo-controlled trial, we compared the efficacy and safety of two dose levels of voxelotor (1500 mg and 900 mg, administered orally once daily) with placebo in persons with sickle cell disease. The primary end point was the percentage of participants who had a hemoglobin response, which was defined as an increase of more than 1.0 g per deciliter from baseline at week 24 in the intention-to-treat analysis. RESULTS: -thalassemia), and approximately two thirds were receiving hydroxyurea at baseline. In the intention-to-treat analysis, a significantly higher percentage of participants had a hemoglobin response in the 1500-mg voxelotor group (51%; 95% confidence interval [CI], 41 to 61) than in the placebo group (7%; 95% CI, 1 to 12). Anemia worsened between baseline and week 24 in fewer participants in each voxelotor dose group than in those receiving placebo. At week 24, the 1500-mg voxelotor group had significantly greater reductions from baseline in the indirect bilirubin level and percentage of reticulocytes than the placebo group. The percentage of participants with an adverse event that occurred or worsened during the treatment period was similar across the trial groups. Adverse events of at least grade 3 occurred in 26% of the participants in the 1500-mg voxelotor group, 23% in the 900-mg voxelotor group, and 26% in the placebo group. Most adverse events were not related to the trial drug or placebo, as determined by the investigators. CONCLUSIONS: In this phase 3 randomized, placebo-controlled trial involving participants with sickle cell disease, voxelotor significantly increased hemoglobin levels and reduced markers of hemolysis. These findings are consistent with inhibition of HbS polymerization and indicate a disease-modifying potential. (Funded by Global Blood Therapeutics; HOPE ClinicalTrials.gov number, NCT03036813.).
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Cites
Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia
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Self-citationIntravascular hemolysis and the pathophysiology of sickle cell disease
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A Phase 3 Trial of l -Glutamine in Sickle Cell Disease
Niihara, Y., Miller, S. T., Kanter, J., Lanzkron, S., Smith, W. R., Hsu, L. L., Gordeuk, V. R., Viswanathan, K., Sarnaik, S., Osunkwo, I., et al. (2018) · New England Journal of Medicine · doi:10.1056/nejmoa1715971 · Cited by 563
Self-citationMortality Rates and Age at Death from Sickle Cell Disease: U.S., 1979–2005
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Sickle cell disease: renal manifestations and mechanisms
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Exagamglogene Autotemcel for Severe Sickle Cell Disease
Frangoul, H., Locatelli, F., Sharma, A., Bhatia, M., Mapara, M., Molinari, L., Wall, D., Liem, R. I., Telfer, P., Shah, A. J., et al. (2024) · New England Journal of Medicine · doi:10.1056/nejmoa2309676 · Cited by 493
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Hemoglobin: Structure, Function and Allostery
Ahmed, M. H., Ghatge, M. S., & Safo, M. K. (2020) · Subcellular Biochemistry · doi:10.1007/978-3-030-41769-7_14 · Cited by 317
Alzahrani, M., Damlaj, M., Jeffries, N., Alahmari, B., Singh, A., Rondelli, D., Tisdale, J. F., Saraf, S. L., & Hsieh, M. M. (2021) · British Journal of Haematology · doi:10.1111/bjh.17311 · Cited by 73
Metadata
- Authors
- Vichinsky, E., Hoppe, C. C., Ataga, K. I., Ware, R. E., Nduba, V., El-Beshlawy, A., Hassab, H., Achebe, M. M., Alkindi, S., Brown, R. C., Diuguid, D. L., Telfer, P., Tsitsikas, D. A., Elghandour, A., Gordeuk, V. R., Kanter, J., Abboud, M. R., Lehrer-Graiwer, J., Tonda, M., Intondi, A., Tong, B., & Howard, J.
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 2019-08-08
- Volume
- 381
- Issue
- 6
- Pages
- 509-519
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W2951288545
- Cited by
- 624
- References
- 19
- FWCI
- 38.32
- Type
- journal article
- Language
- en
- Open access
- bronze
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- Vichinsky, E., Hoppe, C. C., Ataga, K. I., Ware, R. E., Nduba, V., El-Beshlawy, A., Hassab, H., Achebe, M. M., Alkindi, S., Brown, R. C., Diuguid, D. L., Telfer, P., Tsitsikas, D. A., Elghandour, A., Gordeuk, V. R., Kanter, J., Abboud, M. R., Lehrer-Graiwer, J., Tonda, M., . . . Howard, J. (2019). A Phase 3 Randomized Trial of Voxelotor in Sickle Cell Disease. New England Journal of Medicine. https://doi.org/10.1056/nejmoa1903212
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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