Senators on Thursday pressed President Donald Trump’s pick to lead the Food and Drug Administration on the agency’s recent cancellation of a vaccine advisory committee meeting as well as his policy ...
Dr. Marty Makary, President Trump's pick to run the Food and Drug Administration, faced questions from the Senate HELP ...
The policy statement aims to bring more rapid action on personnel and management decisions and empowers HHS and each of its offices and subagencies ...
Words matter. Government-imposed elimination of words and violation of constitutionally-protected free press guarantees ...
Protagonist Therapeutics, Inc. (“Protagonist”) (NASDAQ:PTGX) and Takeda (TSE:4502/NYSE:TAK) today announced positive topline results for the Phase 3 VERIFY study, in which phlebotomy-dependent ...
Full year operating cash flow from continuing operations of $163 million and free cash flow from continuing operations of $70 million ...
Due to federal research cuts, Navy veteran Kyle Lewis says he won't be able to receive the cancer treatment that saved his life.
Life science firm Nuvation Bio raised $250 million to bring its novel lung cancer therapy to market and help it reach ...
Dr. Shai Efrati, a professor of medicine, does experimental treatments in the hope he will age well. But his top tip for ...
The FDA has accepted under Priority Review the NDA for lenacapavir for the prevention of HIV as pre-exposure prophylaxis.
Vantage Specialty Chemicals, Inc., (Vantage) today announced that its VYCERIN™ API Glycerin, USP is listed on the Drug Master File (DMF-040171) with the U.S. Food and Drug Administration (FDA).
To date, the MAGNIFY study ( NCT05893537) has enrolled 100 participants. All participants are completing a final clinic visit in February 2025. Cognition intends to unblind the study at the end of ...
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