drugset / Trial / NCT04381325

A Study of MSB0254 Injection in Advanced Solid Tumors

NCT04381325 ↗

Phase 1 Terminated 25 enrolled Suzhou Transcenta Therapeutics Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

This study was an open, multi-dose dose escalation phase I clinical study to evaluate the safety, tolerability and PK characteristics of MSB0254 in patients with locally advanced or metastatic solid tumors, and to preliminarily measure its anti-tumor efficacy.

Timeline

Start
2020-04-01
Primary completion
2022-06-08
Completion
2022-06-08

Outcome

Outcome not reported

Stopped (Business): “Sponsor Decision”

Drugs

EvaluationDrugModalityDoseRoute
Subject MSB0254 Unknown 4 mg/kg Intravenous
Subject MSB0254 Unknown 8 mg/kg Intravenous
Subject MSB0254 Unknown 12 mg/kg Intravenous
Subject MSB0254 Unknown 16 mg/kg Intravenous
Subject MSB0254 Unknown 20 mg/kg Intravenous

Indications