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Merck & Co's Keytruda rejected by UK NICE in advanced kidney cancer | S&P Global Market Intelligence
FDA Accepts Application for Merck's KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Treatment for Advanced or Unresectable Biliary Tract Cancer
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Merck Receives Accelerated Approval of KEYTRUDA® (pembrolizumab), the First FDA-Approved Anti-PD-1 Therapy
![Moderna on X: "We announced today that mRNA-4157/V940, an investigational personalized #mRNA #cancer vaccine, in combination with KEYTRUDA, @Merck's anti-PD-1 therapy, has been granted Breakthrough Therapy Designation by the U.S. FDA for Moderna on X: "We announced today that mRNA-4157/V940, an investigational personalized #mRNA #cancer vaccine, in combination with KEYTRUDA, @Merck's anti-PD-1 therapy, has been granted Breakthrough Therapy Designation by the U.S. FDA for](https://pbs.twimg.com/media/FpmbQN-WAAEq9jr.jpg:large)
Moderna on X: "We announced today that mRNA-4157/V940, an investigational personalized #mRNA #cancer vaccine, in combination with KEYTRUDA, @Merck's anti-PD-1 therapy, has been granted Breakthrough Therapy Designation by the U.S. FDA for
Moderna and Merck Announce mRNA-4157 (V940), an Investigational Individualized Neoantigen Therapy, in Combination with KEYTRUDA(R) (Pembrolizumab), Demonstrated Superior Recurrence-Free Survival in Patients with High-Risk Stage III/IV Melanoma ...
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Merck's PD-1 Drug Outperforms Ipilimumab for Treatment of Advanced Melanoma - Cancer Research Institute
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KEYTRUDA® (pembrolizumab) Showed Statistically Significant Improvement In Disease-Free Survival Versus Placebo As Adjuvant Treatment For Patients With Stage IB-IIIA Non-Small Cell Lung Cancer Regardless Of PD-L1 Expression 2023 - EORTC
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Hummingbird Bioscience collaborates with Merck for a clinical trial on HMBD-002, our anti-VISTA antibody, in combination with KEYTRUDA®
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