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Phase 3 Trial Launches for Keytruda, MK-1084 in KRAS-Mutant NSCLC

A clinical trial has started to evaluate the investigational drug MK-1084 and Keytruda among some patients with metastatic non-small cell lung cancer.

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Merck (MRK) Initiates Phase 3 Clinical Trial of MK-1084

Merck (MRK) Initiates Phase 3 Clinical Trial of MK-1084
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Merck Initiates Phase 3 Clinical Trial of MK-1084, an Investigational Oral KRAS G12C Inhibitor, in Combination with KEYTRUDA® (pembrolizumab) for First-Line Treatment of Certain Patients With Metastatic Non-Small Cell Lung Cancer

Merck , known as MSD outside of the United States and Canada, today announced it has initiated a Phase 3 clinical trial evaluating MK-1084, an investigational oral selective KRAS G12C inhibitor, in...

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Merck: launches phase III trial in lung cancer -April 04, 2024 at 08:33 am EDT

Merck announced today that it has launched a phase 3 clinical trial evaluating its ' MK-1084 ' in combination with Keytruda for the first-line treatment of selected patients with metastatic non-small...

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REJOICE-Ovarian01 Phase 2/3 Trial of Raludotatug Deruxtecan Initiated in Patients with Platinum-Resistant Ovarian Cancer

Daiichi Sankyo and Merck , known as MSD outside of the United States and Canada, announced today that the first patient has been dosed in the REJOICE-Ovarian01 phase 2/3 trial evaluating the...

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Harpoon Therapeutics : April 3, 2024 -April 03, 2024 at 08:32 am EDT

BASKING RIDGE, N.J. & RAHWAY, N.J., April 3, 2024 - Daiichi Sankyo and Merck , known as MSD outside of the United States and Canada, announced today that the first patient has been...

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Merck: 1st patient in raludotatug study -April 03, 2024 at 09:42 am EDT

Merck and its partner Daiichi Sankyo announced today that the first patient has received a dose in a phase 2/3 trial evaluating the efficacy and safety of the investigational raludotatug deruxtecan ...

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EU Approves Merck's Keytruda For Lung Cancer Chemotherapy

(CTN News) - The European Commission approved Merck's Keytruda anti-PD-1 therapy as a neoadjuvant treatment and monotherapy...................

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European Commission Approves Merck's KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy as Adjuvant Treatment, for Resectable Non-Small Cell Lung Cancer (NSCLC) at High Risk of Recurrence in Adults -March 28, 2024 at 06:46 am EDT

Decision marks the first approval in Europe for an anti-PD-1/L1 therapy in resectable NSCLC based on positive overall survival results and represents the sixth approval for KEYTRUDA in lung cancer in...

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European Commission Approves Merck's KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy as Adjuvant Treatment, for Resectable Non-Small Cell Lung Cancer (NSCLC) at High Risk of Recurrence in Adults

European Commission Approves Merck's KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy as Adjuvant Treatment, for Resectable Non-Small Cell Lung Cancer (NSCLC) at High Risk of Recurrence in Adults
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