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

Recruiting Phase 1 Interventional Study
Solid Tumors With FGFR2 Alterations, Adult
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 75
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
151 (estimated)
Sponsor
KinoTeck Therapeutics Co., Ltd · Industry
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About This Trial
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(part…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Histologically or cytologically confirmed unresectable or metastatic solid tumor * Documented FGFR2 gene fusion, mutation, or amplification per testing of blood and/or tumor * Patient must have measurable disease per RECIST v1.1 * Patient has ECOG performance status of 0-1 * P…
Contacts

Lei Li

0086 13711344347

lilei@kino-biotech.com

CONTACT

Shaohua Chang

0086-13621109316

csh@kino-biotech.com

CONTACT