drugset / Trial / NCT06872580

A Study of QLS1209 in theTreatment of Patients With Advanced Solid Tumors

NCT06872580 ↗

Phase 1 Not yet recruiting 149 enrolled Qilu Pharmaceutical Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

The goal of this clinical trial is to assess the safety and tolerability of QLS1209 alone in patients with eligible advanced solid tumors,determine the maximum tolerated dose (MTD) or maximum drug dose(MAD)of QLS1209, identify a recommended phase 2 dose (RP2D) and preferred schedule, examine preliminary pharmacokinetics (PK) and assess anti-tumor activity.

Timeline

Start
2025-04
Primary completion
2027-04
Completion
2028-04

Drugs

EvaluationDrugModalityDoseRoute
Subject QLS1209 Unknown — —

Indications