FDA grants accelerated approval of mosunetuzumab for relapsed, refractory follicular lymphoma
- PMID: 37088993
- DOI: 10.1002/cncr.34810
FDA grants accelerated approval of mosunetuzumab for relapsed, refractory follicular lymphoma
References
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- FDA grants accelerated approval to mosunetuzumab-axgb for relapsed or refractory follicular lymphoma. News release. US Food and Drug Administration. December 22, 2022. Accessed March 21, 2023. https://www.fda.gov/drugs/resources-information-approved-drugs/fda-grant...
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- Budde LE , Sehn LH , Matasar M , et al. Safety and efficacy of mosunetuzumab, a bispecific antibody, in patients with relapsed or refractory follicular lymphoma: a single-arm, multicentre, phase 2 study. Lancet Oncol. 2022;23(8):1055-1065. doi:10.1016/S1470-2045(22)00335-7
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- Bartlett NL , Sehn LH , Matasar MJ , et al. Mosunetuzumab monotherapy demonstrates durable efficacy with a manageable safety profile in patients with relapsed/refractory follicular lymphoma who received >2 prior therapies: updated results from the pivotal phase II study [abstract 610]. Abstract presented at: 64th ASH Annual Meeting and Exposition; December 10-13, 2022; New Orleans, LA. https://ash.confex.com/ash/2022/webprogram/Paper157691.html
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