News about "dexamethasone "

BMS Reports Positive EXCALIBER-RRMM Results for Zenbexus in Multiple Myeloma

BMS Reports Positive EXCALIBER-RRMM Results for Zenbexus in Multiple Myeloma

Bristol Myers Squibb reported phase 3 EXCALIBER-RRMM results showing higher MRD-negative complete response rates with Zenbexus plus daratumumab and dexamethasone.

Dexamethasone | 28/09/2026 | By News Bureau |  115

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.

Dexamethasone | 14/08/2026 | By News Bureau |  122

FDA Accepts Bristol Myers Squibb's NDA for Iberdomide Combination in Relapsed/Refractory Multiple Myeloma

FDA Accepts Bristol Myers Squibb's NDA for Iberdomide Combination in Relapsed/Refractory Multiple Myeloma

Iberdomide, an investigational oral CELMoD therapy, is under FDA review in combination with daratumumab and dexamethasone for patients with relapsed or refractory multiple myeloma.

Dexamethasone | 19/02/2026 | By News Bureau |  238

J&J's Tecvayli Cuts Death Risk in Phase III Multiple Myeloma Study

J&J's Tecvayli Cuts Death Risk in Phase III Multiple Myeloma Study

Phase III MajesTEC-9 shows Tecvayli significantly improves survival, reducing progression or death risk by 71 percent versus standard care in relapsed multiple myeloma.

Dexamethasone | 15/01/2026 | By News Bureau |  178

Lupin Secures US FDA Approval for Lenalidomide Capsules

Lupin Secures US FDA Approval for Lenalidomide Capsules

The approved Lenalidomide Capsules, bioequivalent to Revlimid by Bristol-Myers Squibb, will be produced at Lupin’s Pithampur site in India.

Dexamethasone, | 17/09/2025 | By Dineshwori |  407

Antengene Gets Malaysian Regulatory Agency Approval for XPOVIO Commercialization

Antengene Gets Malaysian Regulatory Agency Approval for XPOVIO Commercialization

Antengene has announced that Malaysian National Pharmaceutical Regulatory Agency has approved a New Drug Application (NDA) for XPOVIO (selinexor).

Dexamethasone | 06/08/2024 | By Aishwarya |  727


 

 

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