Amendment to require one-firth of the money be devoted to therapeutic review was defeated by the House Energy and Commerce Committee.
Restrictions will not be added to the US Food and Drug Administration’s additional coronavirus funding despite Republican efforts during a markup of the bill in the House Energy and Commerce Committee on 11 February.
Rep. Neal Dunn, R-FL, proposed that $100m of the $500m allocated to the FDA in the bill be reserved...
While treatments for scleroderma are in development, none are approved for the condition that is associated with high morbidity and mortality. The European Medicines Agency says guidance on how to design development programs for the disorder is needed.
Madrigal Pharmaceuticals’ Rezdiffra is on track to become the first medicine approved in the EU for non-cirrhotic metabolic dysfunction-associated steatohepatitis after the European Medicines Agency recommended that it be granted conditional marketing authorization.
Highlights from Day Four of the BIO International Convention include policy concerns helping constrain dealmaking, Novartis discussing its approach to partnering, and Generate looking for funding to move into Phase III.
