drugset / Trial / NCT03710265

SHR-1701 in Metastatic or Locally Advanced Solid Tumors

NCT03710265

Phase 1 Unknown 206 enrolled Jiangsu HengRui Medicine Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

The main purpose of this Phase I study is to access the safety and tolerability of SHR-1701 at different dose levels. It is hoped to find out the recommended dose for Phase II/III.

Timeline

Start
2018-11-20
Primary completion
2022-12-31
Completion
2022-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Retlirafusp alfa Protein / enzyme biologic 1 mg/kg Intravenous
Subject Retlirafusp alfa Protein / enzyme biologic 3 mg/kg Intravenous
Subject Retlirafusp alfa Protein / enzyme biologic 10 mg/kg Intravenous
Subject Retlirafusp alfa Protein / enzyme biologic 20 mg/kg Intravenous
Subject Retlirafusp alfa Protein / enzyme biologic 30 mg/kg Intravenous

Indications