T The stage for Ervebo’s approval was set this October, when a committee assembled by the European Medicines Agency (EMA) recommended a conditional marketing authorization for the vaccine by the EU. Conditional marketing authorizations are given to new drugs or therapies that address an “unmet medical need” for patients. These drugs are approved on a quicker schedule than the typical new drug and Advertisement In Ervebo’s case, though, the data so far revealed the preliminary results of its “Finding a vaccine as soon as possible against this terrible virus has been a priority for the international community ever since Ebola hit West Africa five years ago,” Vytenis Andriukaitis, commissioner in charge of Health and Food Safety at the EU’s European Commission, said in a statem announcing the approval Although the marketing rights for Ervebo are held by Merck, it was originally developed by researchers from the Public Health Agency of Canada, which still maintains non-commercial rights. Advertisement The vaccine’s approval, significantsaid that licensed doses of Ervebo will not be available to the world until the middle of 2020 And while Ervebo may be a highly effective vaccine, the largest hurdles to containing the current Ebola outbreak have been structural. Public… Read full this story
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