Teva Pharmaceuticals (TEVA) and Medincell (MEDCL) announced that the supplemental New Drug Application sNDA for UZEDY extended-release ...
The application leverages existing clinical data for Uzedy along with prior FDA findings on the safety of Udezy in patients ...
Pharmaceuticals, a U.S. affiliate of Teva Pharmaceutical Industries, and Medincell announced that the supplemental New Drug ...
Israel-headquartered Teva Pharmaceutical Industries’ US subsidiary and France’s and Medincell announced that the supplemental ...
UZEDY is currently approved for use every one or two months as a subcutaneous long-acting injectable (LAI) for the treatment ...
Eric Hughes, MD, PhD, Executive Vice President of Global R&D and Chief Medical (TASE:BLWV) Officer at Teva, said, "Since the FDA approval of UZEDY almost two years ago, it has proven to be an ...
The FDA has accepted a supplemental New Drug Application submitted by Teva (NYSE:TEVA) and Medincell (OTC:MDCLF) for Uzedy ...
The company is leaning on its subcutaneous technology to deliver long-acting options that could prevent patients from cycling through drugs.
Parsippany, New Jersey Thursday, February 27, 2025, 13:00 Hrs [IST] ...
Rather than offering patients a new molecule, Uzedy’s breakthrough is tied to its method of delivery. Developed with a technology Teva licensed from Medincell called SteadyTeq, Uzedy offered the ...
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