drugset / Trial / NCT06228846

An Phase I Study of YY001 in Patients with Advanced Solid Tumors

NCT06228846

Phase 1 Completed 16 enrolled Shanghai Yuyao Biotech Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

The safety and tolerability of YY001 in the treatment of patients with advanced solid tumors were evaluated, and the possible dose-limiting toxicity (DLT) and the maximum tolerated dose (MTD) or recommended phase II clinical dose (RP2D) were observed.

Timeline

Start
2022-07-14
Primary completion
2024-04-30
Completion
2024-05-30

Drugs

EvaluationDrugModalityDoseRoute
Subject YY001 Protein / enzyme biologic Oral

Indications

No indication recorded.