Belantamab mafodotin monotherapy for relapsed or refractory multiple myeloma: a real-world observational study in the United States
- PMID: 39415693
- PMCID: PMC11877074
- DOI: 10.3324/haematol.2024.285893
Belantamab mafodotin monotherapy for relapsed or refractory multiple myeloma: a real-world observational study in the United States
References
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- US Food and Drug Administration. FDA granted accelerated approval to belantamab mafodotin-blmf for multiple myeloma. 2020; https://www.fda.gov/drugs/resources-information-approved-drugs/fda-grant.... Accessed November 16, 2023.
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- Lonial S, Lee HC, Badros A, et al. . Belantamab mafodotin for relapsed or refractory multiple myeloma (DREAMM-2): a two-arm, randomised, open-label, phase 2 study. Lancet Oncol. 2020;21(2):207-221. - PubMed
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- European Medicines Agency. EMA recommends non-renewal of authorisation of multiple myeloma medicine Blenrep. 2023; https://www.ema.europa.eu/en/news/ema-recommends-non-renewal-authorisati.... Accessed January 11, 2024.
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- US Food and Drug Administration. Announcement of the revocation of the biologics license for BLENREP. 2023; https://www.govinfo.gov/content/pkg/FR-2023-03-30/pdf/2023-06576.pdf. Accessed December 11. 2023.
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