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Unnatural Products, Inc Enters Research Collaboration with Merck

Unnatural Products, Inc Enters Research Collaboration with Merck
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Keytruda Plus Chemoradiotherapy Approved for FIGO 2014 Stage III-IVA Cervical Cancer

The FDA has approved Keytruda (pembrolizumab) plus chemoradiotherapy for the treatment of patients with FIGO 2014 Stage III-IVA cervical cancer.

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FDA Approves Merck s KEYTRUDA (pembrolizumab) Plus Chemoradiotherapy as Treatment for Patients With FIGO 2014 Stage III-IVA Cervical Cancer

12.01.2024 - Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced the U.S. Food and Drug Administration (FDA) has approved KEYTRUDA, Merck’s anti-PD-1 therapy, in combination with chemoradiotherapy (CRT) for the treatment of .

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FDA Approves Merck s KEYTRUDA® (pembrolizumab) Plus Chemoradiotherapy as Treatment for Patients With FIGO 2014 Stage III-IVA Cervical Cancer

FDA Approves Merck s KEYTRUDA® (pembrolizumab) Plus Chemoradiotherapy as Treatment for Patients With FIGO 2014 Stage III-IVA Cervical Cancer
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FDA Approves Merck s KEYTRUDA® (pembrolizumab) Plus Chemoradiotherapy as Treatment for Patients With FIGO 2014 Stage III-IVA Cervical Cancer -January 12, 2024 at 05:31 pm EST

KEYTRUDA is the first and only anti-PD-1 therapy approved in combination with chemoradiotherapy for these patients Approval marks third FDA-approved indication for KEYTRUDA in cervical cancer and.

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