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(Reuters) -German drugmaker Bayer on Friday won an endorsement by the European Medicines Agency to extend the intervals ...
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Pharmaceutical Technology on MSNBayer’s Eylea set for longer treatment intervals to challenge Roche’s VabysmoAn EMA committee has issued a positive opinion for a label extension that would allow six-month injection intervals for Eylea ...
If approved, Eylea 8 mg would become the only anti-vascular endothelial growth factor (anti-VEGF) treatment in the EU authorized for six-month intervals for both nAMD and DME, according to Bayer ...
This update covers the latest health sector developments, including Moderna's COVID-19 vaccine review, GSK's asthma drug FDA ...
Bayer announces EMA committee recommends label extension approval for Eylea 8 mg: Berlin Monday, May 26, 2025, 17:00 Hrs [IST] Bayer announced that the Committee for Medicinal Pro ...
Berlin: Bayer has received approval from the Center for Drug Evaluation (CDE) of China's National Medical Products ...
Bayer A.G. (OTCPK ... the label expansion of a high-dose version of its ophthalmic drug, Eylea, with an extended 6-month treatment interval. Issuing a so-called positive opinion, EMA’s Committee ...
On the surface, macular degeneration treatment Eylea continued its juggernaut path in 2022. On Tuesday, when Bayer reported fourth quarter earnings, it showed 3.2 billion euros ($3.4 billion ...
Bayer has licensed exclusive marketing rights outside the United States, where the companies share equal profits from the sales of Eylea. Eylea’s intravitreal injection 40 mg/mL has been approved for ...
Increased ocular pressure (5%) was the only ocular treatment-emergent ... developed by Regeneron and Bayer AG. Regeneron maintains exclusive rights to EYLEA and EYLEA HD in the U.S. Bayer has ...
FRANKFURT, Nov 10 (Reuters) - Bayer (BAYGn.DE), opens new tab said on Friday that the European Medicines Agency recommended approval of a higher dose version of eye drug Eylea for treatment of a ...
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