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Discover the latest advancements in breast cancer treatment at the 24th Annual International Congress, featuring expert ...
Perioperative pembrolizumab enhances survival rates in advanced head and neck cancer, paving the way for earlier ...
Keytruda (pembrolizumab) is approved for head and neck squamous cell carcinoma as a perioperative treatment regimen.
The approval introduces the first perioperative anti-PD-1 treatment regimen for adults with resectable locally advanced head ...
RAHWAY, N.J., May 31, 2025--Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced that KEYTRUDA® (pembrolizumab) plus Trodelvy® (sacituzumab govitecan-hziy ...
Alvotech and Dr. Reddy’s have entered into a collaboration and license agreement to co-develop, manufacture and commercialize ...
Merck has received approval from the Food and Drug Administration to expand use of its blockbuster drug, Keytruda, to treat ...
The vaccine is being developed in partnership with Cleveland Clinic and the phase one trial is fully funded by a grant from ...
Alvotech and Dr. Reddy's partner to develop a Keytruda biosimilar, a German court bans Humira biosimilar over patent dispute, ...
News Medical on MSN14d
FDA Approves Keytruda as First Immune Checkpoint Inhibitor for Resectable Locally Advanced Head and Neck CancerPembrolizumab, an immune checkpoint inhibitor, has been approved by the U.S. Food and Drug Administration (FDA) for the ...
Hosted on MSN25d
Alvotech and Dr. Reddy’s partner to co-develop biosimilar candidate for Keytruda (pembrolizumab) - MSNKeytruda (pembrolizumab) is indicated for the treatment of numerous cancer types. In 2024, worldwide sales of Keytruda were $29.5 billion. The collaboration combines Dr. Reddy’s (NYSE:RDY) and ...
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