drugset / Trial / NCT03809767

A Study of CS1003 in Subjects With Advanced Solid Tumors or Lymphomas

NCT03809767

Phase 1 Completed 107 enrolled CStone Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

This is a phase Ia/Ib, open-label, multiple-dose, dose-escalation and expansion study to evaluate the safety, tolerability, pharmacokinetics and anti-tumor activity of CS1003 in subjects with advanced solid tumors or lymphoma.

Timeline

Start
2018-10-29
Primary completion
2021-08-30
Completion
2022-06-13

Drugs

EvaluationDrugModalityDoseRoute
Subject CS1003 Monoclonal antibody 60 mg Intravenous
Subject CS1003 Monoclonal antibody 200 mg Intravenous

Indications