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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 . ....

Daiichi Sankyo , Merck Research Laboratories , Global Clinical Development , Marjorie Green , Senior Vice President , Late Stage Oncology , Merck Research ,

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. ....

Sri Lanka , United States , Daiichi Sankyo , Raludotatug Deruxtecan , Mark Rutstein , European Society For Medical Oncology Congress , Merck Research Laboratories , Sarah Cannon Research Institute , Exchange Commission , Society For Gynecologic Oncology , Statement Of Merck Co Inc , Oncology Clinical Development , Global Clinical Development , Development Innovations In Nashville , Merck Co Inc , European Society , Medical Oncology Congress , Gynecologic Oncology , Global Head , Marjorie Green , Senior Vice President , Late Stage Oncology , Merck Research , North America , Merck Collaboration , Looking Statement ,

Merck (MRK) Reports Patritumab Deruxtecan Granted Priority Review in the U.S.

Merck (MRK) Reports Patritumab Deruxtecan Granted Priority Review in the U.S.
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United States , Ken Takeshita , Daiichi Sankyo , Merck Research Laboratories , Global Clinical Development , Drug Administration , Priority Review , Biologics License Application , Prescription Drug User Fee Act , Breakthrough Therapy Designation , Real Time Oncology Review , Lung Cancer , Global Head , Marjorie Green , Senior Vice President , Late Stage Oncology , Merck Research ,

Patritumab Deruxtecan Granted Priority Review in the U.S. for Certain Patients with Previously Treated Locally Advanced or Metastatic EGFR-Mutated Non-Small Cell Lung Cancer

Patritumab Deruxtecan Granted Priority Review in the U.S. for Certain Patients with Previously Treated Locally Advanced or Metastatic EGFR-Mutated Non-Small Cell Lung Cancer
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United States , Ken Takeshita , Peter Dannenbaum , Koji Ogiwara , Patritumab Deruxtecan , Robert Josephson , Daiichi Sankyo , Jennifer Brennan , Statement Of Merck Co Inc , Daiichi Sankyo Co Ltd , Merck Research Laboratories , International Agency For Research On Cancer , Daiichi Sankyo Inc , Drug Administration , World Health Organization , Global Clinical Development , Merck Co Inc , Exchange Commission , Time Oncology Review , Priority Review , Biologics License Application , Prescription Drug User Fee Act , Breakthrough Therapy Designation , Real Time Oncology Review , Lung Cancer , Global Head ,

Patritumab Deruxtecan BLA Receives Priority Review in NSCLC

The FDA has accepted and granted priority review to the biologics license application seeking the approval of the HER3-directed antibody-drug conjugate patritumab deruxtecan for the treatment of adult patients with locally advanced or metastatic EGFR-mutated non–small cell lung cancer. ....

Ken Takeshita , Daiichi Sankyo , Global Clinical Development , Merck Research Laboratories , Senior Vice President , Late Stage Oncology , Lung Cancer , Clinical Oncology , Prescription Drug User Fee Act , Global Head , Patritumab Deruxtecan , Patients With Locally Advanced Or Metastatic Egfr Mutated Non Small Cell Lung Cancer , Marjorie Green ,