drugset / Trial / NCT06078800

A Study of YL-17231 in Patients With Advanced Solid Tumors

NCT06078800 ↗

Phase 1 Unknown 80 enrolled Shanghai YingLi Pharmaceutical Co. Ltd.
NaSequentialOpen-labelTreatment

Summary

This is a phase 1 open label multicenter study to evaluate the maximum tolerance, safety, tolerance and PK of oral YL-17231 in patients with advanced solid tumors with KRAS mutation, so as to confirm the recommended phase 2 dose of YL-17231 and obtain the preliminary efficacy information of patients with advanced solid tumors with KRAS mutation.

Timeline

Start
2023-09-28
Primary completion
2025-03
Completion
2025-12

Drugs

EvaluationDrugModalityDoseRoute
Subject YL-17231 Unknown 0.25 mg Oral
Subject YL-17231 Unknown 0.5 mg Oral
Subject YL-17231 Unknown 10 mg Oral

Indications