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Merck launches DTC campaign for Keytruda - MM+M - Medical Marketing and  Media
Merck launches DTC campaign for Keytruda - MM+M - Medical Marketing and Media

Merck Hikes Forecast as Keytruda Tops $3 Billion for Quarter - Bloomberg
Merck Hikes Forecast as Keytruda Tops $3 Billion for Quarter - Bloomberg

Merck's PD-1 Drug Outperforms Ipilimumab for Treatment of Advanced Melanoma  - Cancer Research Institute
Merck's PD-1 Drug Outperforms Ipilimumab for Treatment of Advanced Melanoma - Cancer Research Institute

Seagen, Astellas and Merck Announce FDA Acceptance of sBLAs for PADCEV®  (enfortumab vedotin-ejfv) with KEYTRUDA® (pembrolizumab) for the First-Line  Treatment of Certain Patients With Locally Advanced or Metastatic  Urothelial Cancer
Seagen, Astellas and Merck Announce FDA Acceptance of sBLAs for PADCEV® (enfortumab vedotin-ejfv) with KEYTRUDA® (pembrolizumab) for the First-Line Treatment of Certain Patients With Locally Advanced or Metastatic Urothelial Cancer

Merck has high Keytruda hopes outside U.S., but Q1 details sparse | Fierce  Pharma
Merck has high Keytruda hopes outside U.S., but Q1 details sparse | Fierce Pharma

Merck and Eisai Provide Update on Phase 3 LEAP-010 Trial Evaluating KEYTRUDA®  (pembrolizumab) Plus LENVIMA® (lenvatinib) in Patients With Certain Types  of Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma.  firmnews.title_view.
Merck and Eisai Provide Update on Phase 3 LEAP-010 Trial Evaluating KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) in Patients With Certain Types of Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma. firmnews.title_view.

KEYTRUDA® (pembrolizumab) Plus Padcev® (enfortumab vedotin-ejfv) Reduced  Risk of Death by More Than Half Versus Chemotherapy in Patients With  Previously Untreated Locally Advanced or Metastatic Urothelial Cancer |  PharmiWeb.Jobs United States
KEYTRUDA® (pembrolizumab) Plus Padcev® (enfortumab vedotin-ejfv) Reduced Risk of Death by More Than Half Versus Chemotherapy in Patients With Previously Untreated Locally Advanced or Metastatic Urothelial Cancer | PharmiWeb.Jobs United States

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
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

F.D.A. Allows First Use of a Novel Cancer Drug - The New York Times
F.D.A. Allows First Use of a Novel Cancer Drug - The New York Times

FDA Adcom Gives Merck's Keytruda a Surprise Thumbs Down | BioSpace
FDA Adcom Gives Merck's Keytruda a Surprise Thumbs Down | BioSpace

Merck & Co axes Keytruda lung cancer niche amid FDA crackdown | pharmaphorum
Merck & Co axes Keytruda lung cancer niche amid FDA crackdown | pharmaphorum

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
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

Hummingbird Bioscience collaborates with Merck for a clinical trial on  HMBD-002, our anti-VISTA antibody, in combination with KEYTRUDA®
Hummingbird Bioscience collaborates with Merck for a clinical trial on HMBD-002, our anti-VISTA antibody, in combination with KEYTRUDA®

US FDA panel backs Merck & Co.'s Keytruda to treat type of bladder cancer |  S&P Global Market Intelligence
US FDA panel backs Merck & Co.'s Keytruda to treat type of bladder cancer | S&P Global Market Intelligence

Promega collaborate with Merck to develop MSI CDx for use with Keytruda
Promega collaborate with Merck to develop MSI CDx for use with Keytruda

Asco 2018 – Merck's dominance leaves rivals scrabbling for subsets |  Evaluate
Asco 2018 – Merck's dominance leaves rivals scrabbling for subsets | Evaluate

ASCO: Can Keytruda expand further in first-line cervical cancer?
ASCO: Can Keytruda expand further in first-line cervical cancer?

Pharma News | Merck, Sanofi, GSK, Hinova, Endogena, Amylyx
Pharma News | Merck, Sanofi, GSK, Hinova, Endogena, Amylyx

FDA Approves Merck's KEYTRUDA for the Adjuvant Treatment of Patients with  Melanoma with Involvement of Lymph Node | World Pharma Today
FDA Approves Merck's KEYTRUDA for the Adjuvant Treatment of Patients with Melanoma with Involvement of Lymph Node | World Pharma Today

Merck's Keytruda Wins Approval for Yet Another Lung Cancer Indication |  BioSpace
Merck's Keytruda Wins Approval for Yet Another Lung Cancer Indication | BioSpace

Merck, Moderna detail potential skin cancer vaccine progress | AP News
Merck, Moderna detail potential skin cancer vaccine progress | AP News

Merck & Co adds more Ph III data for Keytruda in stomach cancer
Merck & Co adds more Ph III data for Keytruda in stomach cancer

Drugmaker Merck tops 3Q forecasts as Keytruda sales jump 20% | AP News
Drugmaker Merck tops 3Q forecasts as Keytruda sales jump 20% | AP News

Keytruda Approved by FDA for Further Potential Treatments of Mesothelioma |  Mesothelioma Help Cancer Organization
Keytruda Approved by FDA for Further Potential Treatments of Mesothelioma | Mesothelioma Help Cancer Organization

FDA Accepts Application for Merck's KEYTRUDA® (pembrolizumab) Plus  Chemotherapy as Treatment for Advanced or Unresectable Biliary Tract Cancer
FDA Accepts Application for Merck's KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Treatment for Advanced or Unresectable Biliary Tract Cancer

US FDA approves Merck & Co.'s Keytruda in 2 new head, neck cancer uses |  S&P Global Market Intelligence
US FDA approves Merck & Co.'s Keytruda in 2 new head, neck cancer uses | S&P Global Market Intelligence