drugset / Trial / NCT05461794

Study To Investigate the Efficacy and Safety of Sitravatinib in Combination With Tislelizumab in Participants With Esophageal Squamous Cell Carcinoma

NCT05461794

Phase 2 Terminated 96 enrolled BeiGene
RandomizedParallel-groupOpen-labelTreatment

Summary

The study aimed to evaluate the efficacy and safety of sitravatinib in combination with tislelizumab as a second- or third-line treatment for participants with locally advanced, unresectable, or metastatic esophageal squamous cell carcinoma (ESCC) who experienced disease progression following prior systemic chemotherapy.

Timeline

Start
2022-10-03
Primary completion
2024-02-26
Completion
2024-02-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Docetaxel Small molecule 75 mg/m2 Intravenous
Subject Irinotecan Small molecule 125 mg/m2 Intravenous
Subject Sitravatinib Small molecule 100 mg Oral
Subject Tislelizumab Monoclonal antibody 200 mg Intravenous