TKI-based regimens remain the primary approach for metastatic renal cell carcinoma after immune checkpoint inhibitor therapy, ...
The U.S. Food and Drug Administration said on Friday it approved new labeling for Sarepta Therapeutics' gene therapy Elevidys ...
Fondazione Telethon announces the positive opinion issued by the Committee for Medicinal Products for Human Use (CHMP) of the ...
On World Diabetes Day, Sanofi is celebrating an approval recommendation in the EU for Teizeild, a first-in-class drug ...
The SAM-002 trial is a 24-week, multicentre, randomised, placebo-controlled Phase 3 study designed to assess the safety and efficacy of sublingual minoxidil in men with AGA. Participants were ...
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Fondazione Telethon achieves milestone with Waskyra approval for Wiskott-Aldrich Syndrome
Fondazione Telethon announces the positive opinion issued by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) recommending marketing authorization in ...
A new research paper documents the outcomes of five volunteers who continued to receive 40Hz light and sound stimulation for ...
The Maharashtra government will screen 8.66 crore individuals and 1.73 crore households for leprosy from November 17 to ...
Although commonly thought of as a “male” hormone, testosterone is essential for women too—it contributes to libido, sexual ...
Poherdy can be dispensed as a substitute for Perjeta without requiring a prescription change from a health care provider.
A new predictive tool combining amyloid PET data with key clinical factors estimates an individual’s lifetime risk for mild ...
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