drugset / Trial / NCT03020823

To Evaluate the Efficacy and Safety of SCB01A in Subjects With r/m Squamous Cell Head and Neck Cancer

NCT03020823 ↗

Phase 2 Terminated 10 enrolled SynCore Biotechnology Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

The aim of this study is to evaluate the efficacy and safety of i.v. infusion for 24-hour of SCB01A in subjects with squamous cell carcinoma of head and neck who have failed previous platinum based therapies.

Timeline

Start
2017-04-30
Primary completion
2018-11-20
Completion
2018-11-20

Outcome

Outcome not reported

Stopped: “withdrawal by sponsor”

Drugs

EvaluationDrugModalityDoseRoute
Subject SCB01A Unknown 24 mg/m2 Intravenous