drugset / Trial / NCT05488821

Safety, Tolerability and Pharmacokinetics Study of QLH11906 in Patients With Advanced Solid Tumors Harboring MAPK Pathway Alterations.

NCT05488821 ↗

Phase 1 Unknown 40 enrolled Qilu Pharmaceutical Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

This is an open label, phase 1 clinical study to evaluate the safety and tolerability of different doses of QLH11906 monotherapy in patients with relapsed/refractory, unresectable locally advanced or metastatic advanced solid tumors with abnormal MAPK pathway, and determine the Maximum Tolerated Dose (MTD) or Maximum Administered Dose (MAD, if MTD cannot be determined) and Recommended Dose in Phase II Clinical Studies (Recommended Phase II Dose, RP2D).

Timeline

Start
2022-06-14
Primary completion
2024-07-01
Completion
2025-07-01

Drugs

EvaluationDrugModalityDoseRoute
Subject QLH11906 Unknown — Oral

Indications

No indication recorded.