US FDA flags seizure risk with certain Parkinson's drugs, seeks label warnings

March 20 (Reuters) - The U.S. Food and Drug Administration said on Friday it has notified manufacturers of certain ...

Protagonist Therapeutics Announces U.S. FDA Approval of ICOTYDE(TM) (icotrokinra) for the Treatment of Moderate to Severe Plaque Psoriasis

ICOTYDE is the first and only IL-23R targeted oral peptide that delivers complete skin clearance and a favorable safety profile in a once-daily pill Approval supported by four phase 3 studies that met ...
Yahoo

US FDA launches program to boost domestic drug manufacturing

WASHINGTON, Feb 1 (Reuters) - The U.S. Food and Drug Administration on Sunday began accepting requests to participate in its PreCheck pilot program, designed to boost domestic drug supply by ...

US FDA approves Bristol Myers Squibb's cancer drug for Hodgkin's lymphoma

March 20 (Reuters) - The U.S. Food and Drug Administration on Friday approved Bristol Myers Squibb's combination treatment ...
C&EN

March 13 Policy Watch: FDA streamlines its process for approving biosimilar drugs

In another development, 25 states have petitioned to join a lawsuit and defend the EPA’s decision to rescind the climate endangerment finding ...
Yahoo

US FDA to review decades-old food preservative in safety overhaul

Add Yahoo as a preferred source to see more of our stories on Google. FILE PHOTO: FILE PHOTO: Signage is seen outside of the Food and Drug Administration (FDA) headquarters in White Oak, Maryland, ...

US FDA approves GSK's drug for liver disease-related itching

March 19 (Reuters) - The U.S. Food and Drug Administration approved GSK's drug for severe itching caused by a type of liver disease, the company said on Thursday. The drug, branded Lynavoy, was ...

US FDA pushes for new methods to replace animal testing in early drug studies

Food and Drug Administration on Wednesday issued a draft guidance to help companies reduce animal studies of experimental ...