drugset / Trial / NCT05441046

Genakumab Alone and in Combination With Tislelizumab in Patients With Advanced Malignant Solid Tumors

NCT05441046

Phase 1 Unknown 120 enrolled Changchun GeneScience Pharmaceutical Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

This is a phase I, multicenter, open-label dose escalation and expansion study to evaluate genakumab alone and in combination with tislelizumab in adult patients with advanced solid malignancies.

Timeline

Start
2022-06-07
Primary completion
2024-06
Completion
2025-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Genakumab Monoclonal antibody 100 mg Subcutaneous
Subject Genakumab Monoclonal antibody 200 mg Subcutaneous
Subject Genakumab Monoclonal antibody 300 mg Subcutaneous
Subject Tislelizumab Monoclonal antibody 200 mg Intravenous

Indications