drugset / Trial / NCT04357756

A Study to Assess YH001 in Combination With Toripalimab Injection in Subjects With Advanced Solid Tumors

NCT04357756

Phase 1 Completed 29 enrolled Eucure (Beijing) Biopharma Co., Ltd
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label, dose-escalation study of YH001 administered intravenously (IV) in combination with Toripalimab. The study is designed to determine the safety, tolerability and maximum tolerated dose (MTD) or recommended Phase 2 dose (RP2D) of YH001 when administered in combination with Toripalimab to subjects with advanced solid tumors.

Timeline

Start
2020-04-21
Primary completion
2022-10-19
Completion
2022-10-19

Drugs

EvaluationDrugModalityDoseRoute
Subject YH001 Unknown Intravenous
Background Toripalimab Monoclonal antibody 240 mg Intravenous

Indications