drugset / Trial / NCT04877717

A Study of SHR-A1904 in Patients With Advanced Solid Cancer

NCT04877717

Phase 1 Active not recruiting 107 enrolled Shanghai Hengrui Pharmaceutical Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

The study is being conducted to assess the safety and tolerability of SHR-A1904 in patients with advanced solid cancer and to determine the dose-limiting toxicity (DLT), maximum tolerated dose (MTD), and recommended phase II dose (RP2D) of SHR-A1904

Timeline

Start
2021-07-01
Primary completion
2025-12-01
Completion
2025-12-01

Drugs

EvaluationDrugModalityDoseRoute
Subject SHR-A1904 Unknown 6 mg/kg
Subject SHR-A1904 Unknown 8 mg/kg

Indications