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Merck Announces KEYLYNK-008 Trial Evaluating KEYTRUDA (pembrolizumab) Plus LYNPARZA (olaparib) for Patients With Metastatic Squamous Non-Small Cell Lung Cancer to Stop for Futility

07.12.2023 - Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced that it will stop the Phase 3 KEYLYNK-008 trial evaluating KEYTRUDA, Merck’s anti-PD-1 therapy, in combination with maintenance LYNPARZA, a PARP inhibitor, for .

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FDA Approves Merck s KEYTRUDA® (pembrolizumab) Plus Chemotherapy as First-Line Treatment for Locally Advanced Unresectable or Metastatic HER2-Negative Gastric or Gastroesophageal Junction (GEJ) Adenocarcinoma -November 16, 2023 at 05:41 pm EST

Approval based on results from the Phase 3 KEYNOTE-859 trial, which demonstrated significant improvement in overall survival in these patients versus chemotherapy alone Approval marks seventh.

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Merck Receives Positive EU CHMP Opinion for KEYTRUDA® (pembrolizumab) Plus Gemcitabine and Cisplatin as First-Line Treatment for Locally Advanced Unresectable or Metastatic Biliary Tract Cancer

Opinion granted based on positive overall survival results from the Phase 3 KEYNOTE‑966 trial .

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Merck & Co , Inc : Merck Receives Positive EU CHMP Opinion for KEYTRUDA (pembrolizumab) Plus Gemcitabine and Cisplatin as First-Line Treatment for Locally Advanced Unresectable or Metastatic Biliary Tract Cancer

Merck & Co , Inc : Merck Receives Positive EU CHMP Opinion for KEYTRUDA (pembrolizumab) Plus Gemcitabine and Cisplatin as First-Line Treatment for Locally Advanced Unresectable or Metastatic Biliary Tract Cancer
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Legend Biotech : to Showcase Leadership in Multiple Myeloma Treatment at the ASH 2023 Annual Meeting -November 02, 2023 at 09:17 am EDT

Legend Biotech : to Showcase Leadership in Multiple Myeloma Treatment at the ASH 2023 Annual Meeting -November 02, 2023 at 09:17 am EDT
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