drugset / Trial / NCT06800196

A Study of KNT-0916 in Treatment of Unresectable or Metastatic Solid Tumors with FGFR2 Alterations

NCT06800196 ↗

Phase 1 Not yet recruiting 151 enrolled KinoTeck Therapeutics Co., Ltd
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This is a Phase1, open-label, dose escalation and expansion study designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics and preliminary efficacy of KNT-0916 in patients with unresectable or metastatic solid tumors harboring FGFR2 alterations who have failed prior systemic therapy. This study is divided into 2 parts, dose escalation part(part A), dose expansion part(partB).

Timeline

Start
2025-03-31
Primary completion
2027-09-30
Completion
2027-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject KNT-0916 Unknown — Oral

Indications

No indication recorded.