The European Medicines Agency recommended that Amylyx Pharmaceuticals’ ALS drug be rejected within the EU.
The drug, known as Relyvrio in the US and Albrioza in Canada and the EU, did not “convincingly” show that it could slow the worsening of ALS in a clinical trial, the EMA’s Committee for Medicinal Products for Human Use (CHMP) said Friday. As a result, regulators could not say for certain that the benefits outweigh the risks.
To read Endpoints News become a free subscriber
Unlock this article instantly, along with access to limited free monthly articles and our suite of newsletters