Gilead (GILD) announced that the European Medicines Agency has validated for parallel accelerated review the company’s marketing authorization ...
Patients should have faster access to newly developed drugs and medicines and the Government is prepared to adopt new ...
FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced that the European Medicines Agency (EMA) has validated for parallel accelerated review the company’s ...
Foster City, California Tuesday, February 25, 2025, 16:00 Hrs [IST] ...
One of the main challenges identified by the research was that, although the European Medicines Agency (EMA) approves new ...
C3i became the first contract development and manufacturing organization (CDMO) for cell and gene therapies in Canada to ...
Gilead Sciences, Inc. has received conditional marketing authorization from the European Commission (EC) for Seladelpar for the treatment of primary biliary cholangitis (PBC) ...
Gilead Sciences (GILD) said on Friday that the European Commission (EC) granted conditional marketing authorization for ...
TG Therapeutics will announce its financial results for this period in a press release to be issued prior to the call.
Approved, Seladelpar Can Provide an Important Treatment Option for People Living With the Rare Liver Disease in the European Economic Area – ...
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