GU Cancers: Dr. Tito Fojo – ASCO Daily News – Lyssna här – Podtail

Research Triangle Park See full prescribing information for. BLENREP. BLENREP (belantamab mafodotin-blmf) for injection, for intravenous use. Initial U.S. Approval: 2020. WARNING: The U.S. Food and Drug Administration has granted Emergency Use Authorization (EUA) for bamlanivimab and etesevimab together and bamlanivimab alone Nov 9, 2020 Blenrep® [prescribing information]. Research Triangle Park, NC. GlaxoSmithKline. 2020.

Belantamab package insert

2020-01-24 Belantamab Mafodotin is currently FDA approved for use in multiple myeloma patients who have received at least 4 prior therapies, including an anti-CD38 monoclonal antibody, a proteasome inhibitor, and an immunomodulatory agent. It is investigational in all other uses. Patients can click here to locate providers of Belantamab Mafodotin (BLENREP®). DREAMM-7: A Phase III Study of the Efficacy and Safety of Belantamab Mafodotin with Bortezomib and Dexamethasone (BVd) in Patients with Relapsed/Refractory Multiple Myeloma (RRMM) Robert Rifkin,1Kevin Boyd,2Sebastian Grosicki,3Kihyun Kim,4Francesco Di Raimondo,5Meletios Dimopoulos,6Katja Weisel,7Bertrand Arnulf,8Roman Hajek,9Vania Find patient medical information for belantamab mafodotin-blmf intravenous on WebMD including its uses, side effects and safety, interactions, pictures, warnings and user ratings.

GU Cancers: Dr. Tito Fojo – ASCO Daily News – Lyssna här – Podtail

WARNING: OCULAR TOXICITY . See full prescribing information for complete boxed warning. BLENREP Belantamab Mafodotin (Belamaf) Accelerated Approval for Patients with Relapsed or Refractory Multiple Myeloma July 14, 2020 GlaxoSmithKline Oncologic Drug Advisory Committee 2021-04-01 2021-01-01 Belantamab mafodotin is a B-cell maturation antigen (BCMA)-directed antibody and microtubule inhibitor conjugate indicated for the treatment of adult patients with relapsed or refractory multiple BLENREP is a prescription medicine used to treat adults with multiple myeloma who have received at least 4 prior medicines to treat multiple myeloma, and their cancer has come back or did not respond to prior treatment. It is not known if BLENREP is safe and effective in children.

GU Cancers: Dr. Tito Fojo – ASCO Daily News – Lyssna här – Podtail

Referenced with permission from the NCCN Drugs & Biologics Compendium (NCCN Compendium®) for belantamab mafodotin. National Comprehensive Cancer Network, 2021. The NCCN Compendium® is a derivative work of the NCCN Guidelines 1. Blenrep [package insert]. Brentford, Middlesex, UK; GlaxoSmithKline, Ltd; August 2020. Accessed August 2020.

Pipeline insert for details. FDA granted priority review to BLA of belantamab mafodotin. High.
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The NCCN Compendium® is a derivative work of the NCCN Guidelines 1. Blenrep [package insert]. Brentford, Middlesex, UK; GlaxoSmithKline, Ltd; August 2020. Accessed August 2020.

About B-cell maturation antigen (BCMA) Belantamab mafodotin or GSK2857916 is a humanized, afucosylated, IgG1 anti-BCMA monoclonal antibody (belantamab or GSK2857914) conjugated to monomethyl auristatin-F (MMAF).
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GU Cancers: Dr. Tito Fojo – ASCO Daily News – Lyssna här – Podtail

Lonial S, Lee HC, Badros A, et al. Belantamab mafodotin for relapsed or refractory multiple myeloma (DREAMM—2): a … GlaxoSmithKline plc (LSE/NYSE: GSK) announced the US Food and Drug Administration (FDA) has approved BLENREP (belantamab mafodotin-blmf) as a monotherapy treatment for adult patients with relapsed or refractory multiple myeloma who have received at least four prior therapies including an anti-CD38 monoclonal antibody, a proteasome inhibitor and an immunomodulatory agent.

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GU Cancers: Dr. Tito Fojo – ASCO Daily News – Lyssna här – Podtail

Talk to your doctor about the risks of receiving belantamab mafodotin-blmf injection.