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The FDA approved Susvimo 100 mg/mL to treat diabetic retinopathy, according to a press release from Genentech.The approval was supported by positive 1-year data from the phase 3 Pavilion study in ...
1h
Zacks Investment Research on MSNRoche Gets FDA Nod for Label Expansion of Susvimo for Third IndicationRoche RHHBY announced today that the FDA has approved a label expansion of ophthalmology drug Susvimo (ranibizumab injection). The regulatory body approved the drug Susvimo for the treatment of ...
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GlobalData 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 ...
7h
Zacks Investment Research on MSNBayer Gets CHMP Nod for Eylea 8 mg in the EU for 2 Major Eye DiseasesBayer BAYRY announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) ...
The Food and Drug Administration (FDA) has approved Susvimo ® (ranibizumab injection) for the treatment of patients with diabetic retinopathy who have previously responded to at least 2 intravitreal ...
Q2元宇宙社交媒体声量变化 Slideshows ...
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