News about "Multiple Myeloma "

GSK to Acquire Chimagen's Trispecific T-Cell Engager for Multiple Myeloma

GSK to Acquire Chimagen's Trispecific T-Cell Engager for Multiple Myeloma

GSK agrees to acquire global rights to Chimagen Biosciences’ investigational trispecific T-cell engager for multiple myeloma in a deal valued at up to USD 750 million.

Multiple Myeloma | 16/09/2026 | By News Bureau

Bristol Myers Squibb Reports Positive Phase 2 Results for Arlo-cel in Relapsed/Refractory Multiple Myeloma

Bristol Myers Squibb Reports Positive Phase 2 Results for Arlo-cel in Relapsed/Refractory Multiple Myeloma

Bristol Myers Squibb’s arlo-cel demonstrated statistically significant and clinically meaningful responses in patients with quadruple-class exposed relapsed and refractory multiple myeloma.

Multiple Myeloma | 09/09/2026 | By News Bureau |  109

US FDA Grants Accelerated Approval to BMS' ZENBEXUS for Multiple Myeloma

US FDA Grants Accelerated Approval to BMS' ZENBEXUS for Multiple Myeloma

The US Food and Drug Administration (FDA) has granted accelerated approval to Bristol Myers Squibb’s (BMS) ZENBEXUS, a first-in-class CELMoD therapy combined with daratumumab and dexamethasone for multiple myeloma.

Multiple Myeloma | 14/08/2026 | By News Bureau |  121

US FDA Grants Accelerated Approval to BMS' ZENBEXUS for Multiple Myeloma

US FDA Grants Accelerated Approval to BMS' ZENBEXUS for Multiple Myeloma

The US Food and Drug Administration (FDA) has granted accelerated approval to Bristol Myers Squibb’s (BMS) ZENBEXUS, a first-in-class CELMoD therapy combined with daratumumab and dexamethasone for multiple myeloma.

Multiple Myeloma. | 14/08/2026 | By News Bureau |  121

US FDA Approves Subcutaneous Sarclisa for Multiple Myeloma Across All Existing Indications

US FDA Approves Subcutaneous Sarclisa for Multiple Myeloma Across All Existing Indications

Sanofi’s SC formulation becomes the first oncology therapy approved for administration via both an on-body injector and manual subcutaneous injection, offering shorter treatment times for patients.

Multiple Myeloma | 13/07/2026 | By News Bureau

GSK plc Secures China Approval for Blenrep Combination Therapy in Multiple Myelom

GSK plc Secures China Approval for Blenrep Combination Therapy in Multiple Myelom

National Medical Products Administration approves Blenrep with bortezomib and dexamethasone for relapsed or refractory patients, backed by strong phase III trial outcomes.

Multiple Myeloma | 21/04/2026 | By News Bureau |  157

Biocon Biologics Secures US FDA Approval for Denosumab Biosimilars Bosaya and Aukelso

Biocon Biologics Secures US FDA Approval for Denosumab Biosimilars Bosaya and Aukelso

The US Food and Drug Administration (FDA) has approved Biocon Biologics' denosumab biosimilars, Bosaya (denosumab-kyqq) 60 mg/mL injection in a single-dose prefilled syringe (PFS) and Aukelso (denosumab-kyqq) 120 mg/1.7 mL (70 mg/mL) injection in a single-dose vial, biosimilars of Prolia and Xgeva, respectively.

Multiple Myeloma | 17/09/2025 | By Dineshwori |  548

Amneal Launches BORUZU for Multiple Myeloma and Mantle Cell Lymphoma

Amneal Launches BORUZU for Multiple Myeloma and Mantle Cell Lymphoma

BORUZU™ (bortezomib injection), a proteasome inhibitor, is used for the treatment of multiple myeloma and mantle cell lymphoma.

Multiple Myeloma | 07/04/2025 | By Aishwarya |  390


 

 

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