The Committee For Medicinal Products For Human Use Of The European Medicines Agency Has Confirmed Its June 2024 Negative Opinion On Apellis Pharmaceuticals' Intravitreal Pegcetacoplan For Geographic Atrophy Secondary To Age-related Macular Degeneration
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The European Medicines Agency's Committee for Medicinal Products for Human Use has upheld its negative opinion on Apellis Pharmaceuticals' intravitreal pegcetacoplan for treating geographic atrophy secondary to age-related macular degeneration.
September 20, 2024 | 9:02 am
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The European Medicines Agency's committee has confirmed its negative opinion on Apellis Pharmaceuticals' pegcetacoplan, impacting its potential market approval in Europe.
The confirmation of a negative opinion by the EMA's committee significantly reduces the likelihood of pegcetacoplan's approval in Europe, which could negatively impact Apellis Pharmaceuticals' stock price due to reduced market potential and investor sentiment.
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