FDA approves leucovorin for rare genetic condition
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Sen. Josh Hawley, R-Mo., introduced a bill to ban the abortion pill mifepristone, calling it "inherently dangerous" and citing research on serious side effects.
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FDA approves GSK’s Wellcovorin for cerebral folate deficiency
FDA worked with GSK to update Wellcovorin labelling for safe, effective use in adult and paediatric CFD-FOLR1 patients.
About five months after U.S. Department of Health and Human Services Secretary Robert F. Kennedy Jr. | About five months after U.S. Health Secretary Robert F. Kennedy Jr. touted leucovorin as “an exciting therapy that may benefit large numbers of children who suffer from autism” during a White House press conference,
U.S. Food and Drug Administrator Marty Makary called on the agency to close a loophole for companies often used to secure product approval.
WASHINGTON — Sen. Josh Hawley rolled out long-shot legislation this week to override the Food and Drug Administration’s approval of mifepristone, part of a two-drug regimen responsible for the majority of abortions in the US. Hawley (R-Mo.
WASHINGTON — Sen. Josh Hawley rolled out long-shot legislation this week to override the Food and Drug Administration’s approval of mifepristone, part of a two-drug regimen responsible for the majority of abortions in the US. Hawley (R-Mo.), flanked by ...
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BMS gains FDA approval for Sotyktu in psoriatic arthritis treatment
The FDA granted the approval following findings from the pivotal POETYK PsA-I and POETYK PsA-II Phase III studies.
Johnson & Johnson (J&J) has announced the US Food and Drug Administration (FDA) approval for the combination of Tecvayli (teclistamab-cqyv) and Darzalex Faspro (daratumumab and hyaluronidase-fihj) for adults with relapsed or refractory multiple myeloma (r/r MM).