The Directorate General of Drug Administration (DGDA) has issued marketing authorisation for the first-ever Covid-19 pill molnupiravir to two pharmaceutical companies in the country.

The U.S. Food and Drug Administration said on Tuesday that it is investigating reports of two deaths due to acute liver failure in non-ambulatory Duchenne muscular dystrophy patients after ...

Amgen has reported positive phase 3 results with its biosimilar version of AstraZeneca/Alexion's blockbuster rare disease drug Soliris, setting up a regulatory filing with the FDA. The biotech has ...

Even though scientists are continually trying to minimize the use of animals and to replace them with non-animal alternatives, animal research remains critical and necessary to comply with legal ...

We extracted data on details of the populations, interventions, comparisons, outcomes of significance to the mental disorder, study methods, cannabinoid dose and route of administration, placement in ...