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DEGEVMA

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Representative image: Bone imaging and oncology treatment planning illustrate Teva’s FDA approval of DEGEVMA, a denosumab biosimilar to Xgeva for cancer-related bone disease.

Pharma & Biotech

Teva wins FDA approval for DEGEVMA biosimilar across all Xgeva indications

by Soujanya Ravi
September 28, 2026
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FDA approves Teva’s DEGEVMA as an Xgeva biosimilar across oncology bone-disease indications, expanding its U.S. denosumab portfolio.

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Pharma & Biotech

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Representative image of biopharma laboratory research. Gilead Sciences and Merck’s latest Phase 3 updates highlight the promise of once-weekly HIV treatment with islatravir and lenacapavir, while raising fresh questions over Trodelvy’s lung cancer expansion strategy.

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AstraZeneca clinical trials Eli Lilly and Company European Medicines Agency FDA FDA approval immunotherapy Inc. Johnson & Johnson medical devices non-small cell lung cancer oncology precision oncology U.S. Food and Drug Administration United States Food and Drug Administration

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