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RECRUITING
NCT06800196
PHASE1

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

Sponsor: KinoTeck Therapeutics Co., Ltd

View on ClinicalTrials.gov

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).

Official title: A Phase I, Multicenter, Open-label Study to Evaluate the Safety, Pharmacokinetics, Preliminary Efficacy of KNT-0916 in Subjects With Unresectable or Metastatic Solid Tumors With FGFR2 Alterations

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

151

Start Date

2025-04-10

Completion Date

2027-12-31

Last Updated

2026-08-05

Healthy Volunteers

No

Interventions

DRUG

KNT-0916

• KNT-0916 is an oral inhibitor of FGFR2.

Locations (1)

Sun Yat-sen University Cancer Center

Guangzhou, Guangdong, China