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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 ...
The FDA and CDC recommended a pause for Ixchiq, a chikungunya vaccine, following reports of adverse events in recipients 60 ...
1d
Clinical Trials Arena on MSNEMA approves Moleculin’s application for Phase IIb/III AML trialThe European Medicines Agency (EMA) has approved Moleculin Biotech’s clinical trial application (CTA) for a pivotal, ...
2hon MSN
A recent study by the University of Turku and the University of Helsinki in Finland and the Finnish Social Insurance ...
Reports of severe adverse events in some people who received the chikungunya vaccine have spurred regulators in Europe and ...
5d
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) ...
Moleculin Biotech, Inc., (Nasdaq: MBRX) ("Moleculin” or the "Company”), a late-stage pharmaceutical company with a broad ...
The FDA and CDC have also recommended pausing the use of Ixchiq in seniors 60 years and older while safety investigations are ...
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 ...
Demand for reliable sterilization methods is climbing fast, driven by the surge in surgeries, rise in hospital-acquired infections, and tighter government oversight, says SNS Insider.Austin, May 14, ...
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