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US FDA warns on risks linked to sulfite-containing compounded drugs
Reuters· 7 hours agoThe U.S. Food and Drug Administration said on Wednesday it had alerted healthcare professionals,...
The FDA should stop letting drug companies skip steps - The Boston Globe
The Boston Globe· 2 days agoThe FDA approves some new medical treatments quickly, before confirmatory trials are carried out, to...
Small Business - Shelby County Reporter | Shelby County Reporter
The Shelby County Reporter· 18 hours agoFDA Approved Phase II/III Clinical Study of KPG-121 in Combination with Abiraterone as a First Line Treatment for mCRPC PR Newswire HEFEI, China, June 5 ...
Customs: Nearly $900K in non-FDA approved Ozempic seized in Cincinnati
FOX 19 Cincinnati· 13 hours agoEleven shipments of a popular pre-filled type 2 diabetes drug were seized by Cincinnati officers of...
FDA panel rejects first MDMA treatment amid deep concerns about flawed trials
NBC NEWS· 1 day agoIf approved by the FDA, it would be the first new treatment for PTSD in more than two decades. The...
FDA panel rejects the use of psychedelic drug MDMA to treat patients with PTSD
Scripps News via AOL· 15 hours agoA panel of advisers to the U.S. Food and Drug Administration has voted against the use of MDMA —...
FDA advisers vote against recommending approval of MDMA as treatment for PTSD
ABC News via Yahoo News· 1 day agoA panel of independent advisers for the U.S. Food and Drug Administration voted against recommending...
FDA Panel Rejects MDMA-Assisted Therapy For PTSD
Forbes· 1 day agoTherapeutics, a company formed by the Multidisciplinary Association for Psychedelic Studies (MAPS) to develop the treatment. After listening to public...
FDA Panel to Consider Updating COVID-19 Jabs for New Virus Strains
Zacks via Yahoo Finance· 2 days agoAn FDA panel meeting is scheduled on Jun 5 to consider if COVID-19 vaccines should be updated to...
Psychedelic Drug Stocks Plummet On FDA Advisers' Doubts About Ecstasy Candidate
The Wall Street Journal· 14 hours agoThe stocks fell after experts advising the FDA on Tuesday evening voted against a drug application...