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Be Bio’s haemophilia B treatment gains FDA orphan drug status
Pharmaceutical Technology via Yahoo Finance· 1 hour agoThe US Food and Drug Administration (FDA) has granted orphan drug designation ...
MDMA therapy wait goes on as FDA panel rejects Lykos’ PTSD treatment
Pharmaceutical Technology via Yahoo Finance· 1 hour agoA US Food and Drug Administration (FDA) panel has voted to decline approval of Lykos Therapeutics's...
FDA advisers vote against recommending approval of MDMA as treatment for PTSD
ABC News via Yahoo News· 14 hours agoA panel of independent advisers for the U.S. Food and Drug Administration voted against recommending...
FDA advisors reject MDMA therapy for PTSD, amid concerns over research
MPR News· 27 minutes agoA panel of experts advising the Food and Drug Administration on the use of the psychedelic MDMA for post-traumatic ...
Panel rejects psychedelic drug MDMA as a PTSD treatment in possible setback for advocates
The Cleveland Plain Dealer· 21 minutes agoA panel of advisers to the Food and Drug Administration voted 10-1 against the overall benefits of MDMA when used ...
FDA panel rejects MDMA-based treatment for PTSD
The Hill· 9 hours agoThe Food and Drug Administration (FDA) panel voted 10-1 against endorsing the safety of MDMA in ...
Soft drinks recall update as FDA sets risk level
Newsweek· 23 hours agoThree soft drink products that were recalled by the Food and Drug Administration (FDA) for containing ...
FDA Panel Rejects MDMA Therapy For PTSD, Citing Concerns Over Research Data In Setback For Advocates
Benzinga· 9 hours agoA committee of advisors to the U.S. Food and Drug Administration (FDA) dealt a blow to the...
Jeffrey Bucholtz on Food and Drug Administration (FDA) | JD Supra
JD Supra· 2 days agoJD Supra is a legal publishing service that connects experts and their content with broader audiences of professionals, journalists and associations. This ...
US health experts vote against MDMA as treatment for PTSD
AFP via Yahoo News· 12 hours agoA panel of US health experts convened by the Food and Drug Administration on Tuesday overwhelmingly...