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Generics & Biosimilars
Access, interchangeability, litigation, and pricing dynamics for follow‑ons.
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Teva’s Second Denosumab Biosimilar FDA-Approved
5+ day, 22+ hour ago (216+ words) Home / News / BioBlast® On 28 September 2026, Teva announced that it has strengthened its position in the biosimilars market with the FDA approval of its internally developed Degevma™ (denosumab-adet), biosimilar to Amgen’s Xgeva®. Degevma™ is indicated for all approved reference indications and…...