On December 14, 2023, Apellis Pharmaceuticals, Inc. (?Apellis?) provided an update on the ongoing review of its marketing authorization application, or MAA, for intravitreal pegcetacoplan for the treatment of geographic atrophy secondary to age-related macular degeneration by the Committee for Medicinal Products for Human Use, or the CHMP, of the European Medicines Agency.
Real-time Estimate
Other stock markets
|
5-day change | 1st Jan Change | ||
40.13 USD | -1.18% | -5.19% | -32.59% |
EPS Revisions
1st Jan change | Capi. | |
---|---|---|
-32.59% | 492.87Cr | |
-1.64% | 9.03TCr | |
-1.97% | 3.95TCr | |
-16.12% | 3.17TCr | |
+61.28% | 2.64TCr | |
-22.79% | 1.43TCr | |
-9.16% | 1.29TCr | |
-11.77% | 1.18TCr | |
-45.97% | 1.1TCr | |
+3.30% | 884.67Cr |
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- Apellis Pharmaceuticals, Inc. Provides Update on Ongoing Regulatory Review of Pegcetacoplan for GA in the European Union