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On June 22, 2021, Merck & Co.
The press release states that Keytruda is the first cancer immunotherapy in this patient group that has achieved positive results as a first-line treatment
Keytruda is a blockbuster anti-PD-1 therapy developed by Merck.
This randomized, double-blind, pivotal phase 3 trial of KEYNOTE-826 enrolled 617 adult patients who have not received systemic chemotherapy and are no longer suitable for radical treatment (such as surgery and/or radiotherapy)
Cervical cancer is one of the most common cancers among women in the world.
Note: The original text has been deleted
Reference materials:
[1] Merck Announces Phase 3 KEYNOTE-826 Trial Met Dual Primary Endpoints of Overall Survival (OS) and Progression-Free Survival (PFS) in Patients With Persistent, Recurrent or Metastatic Cervical Cancer.