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Home»Posts tagged with»multiple myeloma

Johnson & Johnson strengthens its multiple myeloma franchise with TECVAYLI and DARZALEX FASPRO approval. What clinicians are watching next

By Pallavi Madhiraju on March 9, 2026   Pharma & Biotech  

Johnson & Johnson strengthens its multiple myeloma franchise with TECVAYLI and DARZALEX FASPRO approval. What clinicians are watching next

FDA approves TECVAYLI plus DARZALEX FASPRO for relapsed multiple myeloma. Discover what the MajesTEC-3 data means for future immunotherapy strategies.

J&J’s Tecvayli-Darzalex Faspro combination approved for myeloma after MajesTEC-3 Phase 3 results

By Pallavi Madhiraju on March 6, 2026   Pharma & Biotech  

J&J’s Tecvayli-Darzalex Faspro combination approved for myeloma after MajesTEC-3 Phase 3 results

FDA approves J&J’s teclistamab plus daratumumab for relapsed myeloma from second line. Analyse the MajesTEC-3 data, safety profile, and what this changes for treatment.

Why Gilead Sciences’ Arcellx acquisition reshapes the competitive dynamics of BCMA CAR T therapy

By Pallavi Madhiraju on February 24, 2026   Pharma & Biotech  

Why Gilead Sciences’ Arcellx acquisition reshapes the competitive dynamics of BCMA CAR T therapy

Gilead Sciences’ acquisition of Arcellx signals a strategic shift in CAR T therapy control and scale. Find out what it changes for multiple myeloma.

Starton Therapeutics advances STAR-LLD as delivery innovation in multiple myeloma

By Soujanya Ravi on February 19, 2026   Pharma & Biotech  

Starton Therapeutics advances STAR-LLD as delivery innovation in multiple myeloma

Starton Therapeutics advances STAR-LLD in Phase 2a. Explore how continuous lenalidomide delivery could reshape multiple myeloma care.

Bristol Myers Squibb pushes CELMoD frontier as FDA accepts iberdomide NDA in relapsed multiple myeloma

By Pallavi Madhiraju on February 18, 2026   Pharma & Biotech  

Bristol Myers Squibb pushes CELMoD frontier as FDA accepts iberdomide NDA in relapsed multiple myeloma

FDA accepts Bristol Myers Squibb’s iberdomide NDA for relapsed multiple myeloma. Find out what this CELMoD filing could change next.

Johnson & Johnson expands DARZALEX FASPRO label with new D-VRd approval in newly diagnosed myeloma

By Pallavi Madhiraju on January 28, 2026   Pharma & Biotech  

Johnson & Johnson expands DARZALEX FASPRO label with new D-VRd approval in newly diagnosed myeloma

Find out how DARZALEX FASPRO’s FDA approval for transplant-ineligible myeloma patients could shift frontline treatment standards.

Johnson & Johnson’s TECVAYLI may redefine second-line myeloma care after MajesTEC-9

By Pallavi Madhiraju on January 15, 2026   Pharma & Biotech  

Johnson & Johnson’s TECVAYLI may redefine second-line myeloma care after MajesTEC-9

TECVAYLI outperformed standard regimens in relapsed/refractory myeloma. Find out what the Phase 3 MajesTEC-9 trial means for future treatment lines.

Can Vyriad’s VV169 redefine CAR T therapy with single-dose in vivo delivery?

By Pallavi Madhiraju on January 1, 2026   Pharma & Biotech  

Can Vyriad’s VV169 redefine CAR T therapy with single-dose in vivo delivery?

Vyriad secures $85M to launch VV169, its in vivo CAR T therapy for multiple myeloma. Find out how this platform could reshape cancer immunotherapy.

Johnson & Johnson targets earlier-line myeloma with CARVYKTI expansion

By Venkatesh B on December 6, 2025   Medical Devices & Diagnostics  

Johnson & Johnson targets earlier-line myeloma with CARVYKTI expansion

Johnson & Johnson’s CARVYKTI shows 80 percent treatment-free survival at 30 months in second-line myeloma. Is CAR-T moving to earlier use?

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