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The FDA did not respond to a request for comment. U.S. Health Secretary Robert F. Kennedy Jr. has said that the agency's ...
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Stocktwits on MSNMoleculin Biotech Gets EMA Nod For Leukemia Trial: Retail Feels Bullish On ‘Low And Slow’ SetupRetail chatter around Moleculin Biotech surged on Monday after the company said the European Medicines Agency had approved ...
The European Union's health regulator said on Wednesday it was reviewing French drugmaker Valneva's chikungunya vaccine after ...
Moleculin Biotech, Inc., (Nasdaq: MBRX) ("Moleculin” or the "Company”), a late-stage pharmaceutical company with a broad ...
The European drugs regulator said on Thursday its safety panel has confirmed suicidal thoughts as a side effect of ...
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MedPage Today on MSNDrug Used by Trump Has Suicide Risk; FDA's 'Aggressive' AI Rollout; 1K Measles CasesThoughts of suicide was confirmed as a side effect of finasteride (Propecia, Proscar), the European Medicines Agency (EMA) ...
On the heels of similar moves in France and the European Union, U.S. health authorities are calling for a pause in the use of ...
Few areas of healthcare are as sensitive as cancer treatment. Each year, around 44,000 cancer tumours are diagnosed here.
Saint Herblain (France), May, 07 2025 – Valneva SE (Nasdaq: VALN; Euronext Paris: VLA), a specialty vaccine company, today announced that the European Medicines Agency (EMA) has started a review ...
Ireland’s Health and Safety Executive has criticised a new report revealing the country’s shocking last place in Western Europe for new oncology drug access.
Some U.S. biotech companies are considering moving early-stage trials of new medicines outside the United States as worry ...
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