Regulatory ApprovalFormycon receives regulatory approval in the UK for FYB203 (aflibercept), a biosimilar to Eylea®, under the brand name AHZANTIVE® 25.02.2025 / 06:30 CET/CESTThe issuer is solely ...

In February 2025, Teva Pharmaceuticals and Alvotech announced ... because of the potential risk for shedding from the household contact and transmission to patient. Non-live vaccinations received ...

In October 2024, the U.S. Food and Drug Administration (FDA) approved SELARSDI™for all indicationsmatching the reference product ...

This marks the second biosimilar released in the U.S. by the strategic partnership between Teva Pharmaceuticals and ... for shedding from the household contact and transmission to patient.

New research by Teva Pharmaceuticals Europe shows that 46% of generic medicines from the EU Critical List of Medicines are supplied by only one provider. This ...

Radiation-Induced Myelosuppression Treatment MarketThe global Radiation-Induced Myelosuppression Treatment Market is ...

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New York, New York-- (Newsfile Corp. - February 25, 2025) - Leading securities law firm Bleichmar Fonti & Auld LLP announces that a lawsuit has been filed against Semtech Corp. (NASDAQ: SMTC) and ...

Piper Sandler analyst David Amsellem reiterated the Overweight rating on Teva Pharmaceutical Industries ... the goal is to address a wide ulcerative colitis and Crohn’s disease patient audience.

With an ROE of -7.03%, the company may need to address challenges in generating satisfactory returns for shareholders. Return on Assets (ROA): Teva Pharmaceutical Indus's ROA is below industry ...