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FDA approves Keytruda regimen for patients with advanced biliary tract cancer

FDA approves Keytruda regimen for patients with advanced biliary tract cancer
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Merck (MRK) Announces FDA Approval of KEYTRUDA Plus Gemcitabine and Cisplatin as Treatment for Patients With Locally Advanced Unresectable or Metastatic Biliary Tract Cancer

Merck (MRK) Announces FDA Approval of KEYTRUDA Plus Gemcitabine and Cisplatin as Treatment for Patients With Locally Advanced Unresectable or Metastatic Biliary Tract Cancer
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FDA Approves Keytruda Plus Chemo for Locally Advanced, Metastatic Biliary Tract Cancer

The Food and Drug Administration approved Keytruda plus chemotherapy for patients with locally advanced unresectable or metastatic biliary tract cancer.

FDA Approves Merck s KEYTRUDA® (pembrolizumab) Plus Gemcitabine and Cisplatin as Treatment for Patients With Locally Advanced Unresectable or Metastatic Biliary Tract Cancer

Approval based on results from the Phase 3 KEYNOTE-966 trial, which demonstrated significant overall survival benefit in these patients versus chemotherapy aloneApproval marks sixth gastrointestinal cancer indication for KEYTRUDA-based regimens in the USRAHWAY, N.J. (BUSINESS WIRE) $MRK #MRK Merck (NYSE: MRK), kn.

FDA Approves Pembrolizumab Plus Chemotherapy for Locally Advanced Unresectable or Metastatic Biliary Tract Cancer

The FDA has approved pembrolizumab (Keytruda) plus gemcitabine and cisplatin for the treatment of patients with locally advanced unresectable or metastatic biliary tract cancer.

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