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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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FDA Approves Merck's KEYTRUDA for the Adjuvant Treatment of Patients with Melanoma with Involvement of Lymph Node | World Pharma Today
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Keytruda Approved by FDA for Further Potential Treatments of Mesothelioma | Mesothelioma Help Cancer Organization
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US FDA panel backs Merck & Co.'s Keytruda to treat type of bladder cancer | S&P Global Market Intelligence
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Merck Receives Accelerated Approval of KEYTRUDA® (pembrolizumab), the First FDA-Approved Anti-PD-1 Therapy
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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
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PRESS RELEASE: KEYTRUDA® (pembrolizumab) Reduced The Risk Of Distant Metastasis Or Death By 40% Compared Versus Placebo As Adjuvant Treatment In Resected, High-Risk Stage III Melanoma 2023 - EORTC
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Merck's PD-1 Drug Outperforms Ipilimumab for Treatment of Advanced Melanoma - Cancer Research Institute
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