2020-07-14

Learn about BLENREP (belantamab mafodotin-blmf) for appropriate patients with relapsed or refractory multiple myeloma. See Full Safety and Prescribing Info, including BOXED WARNING.

Blenrep (belantamab mafodotin-blmf) is a B-cell maturation antigen (BCMA)-directed antibody and microtubule inhibitor 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. Package insert. GlaxoSmithKline; 2020. 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. Background: Belantamab mafodotin (GSK2857916), an immunoconjugate targeting B-cell maturation antigen, showed single-agent activity in the phase 1 DREAMM-1 study in heavily pre-treated patients with relapsed or refractory multiple myeloma.

Belantamab package insert

Belantamab mafodotin is the first BCMA-targeted antibody-drug conjugate with a humanized anti-BCMA monoclonal antibody (mAb) conjugated to the microtubule inhibitor mafodotin. 2,5 Belantamab mafodotin specifically binds to BCMA and eliminates myeloma cells by a multimodal mechanism. Belantamab mafodotin is the first BCMA-targeted antibody-drug conjugate with a humanized anti-BCMA monoclonal antibody (mAb) conjugated to the microtubule inhibitor mafodotin. 2,5 Belantamab mafodotin specifically binds to BCMA and eliminates myeloma cells by a multimodal mechanism.

Jan 1, 2021 BLENREP® (belantamab mafodotin-blmf) Prior Auth Criteria Absence of unacceptable toxicity from the drug. Blenrep [package insert]. Dec 22, 2020 Package insert.

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.

Medscape - Multiple myeloma dosing for Blenrep (belantamab mafodotin), frequency-based adverse effects, comprehensive interactions, contraindications, pregnancy & lactation schedules, and cost information. 2020-07-29 · A Phase 1b clinical trial evaluating GlaxoSmithKline (GSK)’s belantamab mafodotin, in combination with SpringWorks Therapeutics’ nirogacestat, in people with relapsed or refractory multiple myeloma, has dosed its first patient, SpringWorks announced. The safety and preliminary effectiveness of On July 24, 2020, the European Medicines Agency (EMA)’s Committee for Medicinal Products for Human Use recommended granting a conditional marketing authorization in the European Union for belantamab mafodotin, a first-in-class, anti-BCMA immunoconjugate, for the treatment of patients with relapsed and refractory multiple myeloma (RRMM) who are no longer responsive to immunomodulatory agents Early data from the DREAMM-6 study suggest that the combination of belantamab mafodotin, bortezomib, and dexamethasone is active in patients with relapsed or refractory multiple myeloma (MM).

Most recently, however, we did have the first BCMA targeted drug, belantamab mafodotin or belamaf, which is an antibody-drug conjugate. Similar to other

If you experience a serious side effect, you or your doctor may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online ( [WEB] ) or by phone (1-800-332-1088). These results were observed in patients receiving the recommended dose of 2.5 mg/kg.

The NCCN Compendium® is a derivative work of the NCCN Guidelines 1. Blenrep [package insert].
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Blenrep (belantamab mafodotin-blmf) 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 myeloma. Issued: London UK. GlaxoSmithKline 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. Lactation: There is no data on the presence of belantamab mafodotin-blmf in human milk or the effects on the breastfed child or milk production. Because of the potential for serious adverse reactions in the breastfed child, advise women not to breastfeed during treatment with BLENREP and for 3 months after the last dose.

Background: Belantamab mafodotin (GSK2857916), an immunoconjugate targeting B-cell maturation antigen, showed single-agent activity in the phase 1 DREAMM-1 study in heavily pre-treated patients with relapsed or refractory multiple myeloma. We further investigated the safety and activity of belantamab mafodotin in the DREAMM-2 study. Belantamab mafodotin is a humanised IgG1 monoclonal antibody-drug conjugate (ADC) developed by GlaxoSmithKline, for the treatment of multiple myeloma and other Belantamab mafodotin - GlaxoSmithKline - AdisInsight The recommended belantamab mafodotin-blmf dose is 2.5 mg/kg as an intravenous infusion over approximately 30 minutes once every 3 weeks. View full prescribing information for BLENREP.
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BELANTAMAB MAFODOTIN-BLMF: 2.5MG/KG: INJECTABLE;INTRAVENOUS: Prescription: None No: No

Accessed January 2021. 2. Referenced with permission from the NCCN Drugs & Biologics Compend ium (NCCN Compendium®) for belantamab mafodotin. National Comprehensive Cancer Network, 2021. The NCCN Compendium® is a derivative work of the NCCN Guidelines Belantamab Mafodotin (Belamaf) Clinical Safety Results Hesham A. Abdullah, MD, MSc, RAC Senior Vice President Head of Clinical Development Oncology GlaxoSmithKline PLC. CO-33 Belamaf 3.4 mg/kg Learn about BLENREP (belantamab mafodotin-blmf) for appropriate patients with relapsed or refractory multiple myeloma.

2021-04-01 · 1. Blenrep [package insert]. Brentford, Middlesex, UK; GlaxoSmithKline, Ltd; August 2020. Accessed January 2021. 2. Referenced with permission from the NCCN Drugs & Biologics Compend ium (NCCN Compendium®) for belantamab mafodotin. National Comprehensive Cancer Network, 2021. The NCCN Compendium® is a derivative work of the NCCN Guidelines®. NATIONAL

GlaxoSmithKline; 2020. Lonial S, Lee HC, Badros A, et al. Belantamab mafodotin for relapsed or refractory multiple myeloma ( Belantamab mafodotin is an investigational anti-B-cell maturation antigen (BCMA ) antibody-drug conjugate in Phase II clinical development for patients with Most recently, however, we did have the first BCMA targeted drug, belantamab mafodotin or belamaf, which is an antibody-drug conjugate.

Company: GlaxoSmithKline. Treatment for: Multiple Myeloma.