CSPC Megalith Biopharmaceutical registers Phase III trial of enlonstobart with SYS6010
The trial plans to enroll 585 participants, beginning on December 30, 2026, with a primary completion date of December 30, 2029. It is a randomized, controlled, double-blind, multicenter Phase III study evaluating the efficacy and safety of enlonstobart with or without SYS6010 in participants with pathologically residual esophageal squamous cell carcinoma after complete surgical resection.
Primary source
ClinicalTrials.gov registry record, November 9, 2026
A Randomized, Controlled, Double-Blind, Multicenter Phase III Clinical Trial to Evaluate the Efficacy and Safety of Enlonstobart, With or Without SYS6010 as Adjuvant Therapy, in Participants With Pathologically Residual Esophageal Squamous Cell Carcinoma Following Complete Surgical Resection
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