RecruitingPhase 2NCT07406633

KQB198 in Combination With Imatinib in Participants With Advanced/Metastatic GIST in 1st Line Setting

A Phase 2, Multicenter, Study Evaluating the Efficacy, Safety, Tolerability, Pharmacokinetics of KQB198 in Combination With Imatinib in Participants With Advanced/Metastatic GI Stromal Tumor in 1st Line Setting


Sponsor

Kumquat Biosciences Inc.

Enrollment

46 participants

Start Date

May 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This study will test an experimental drug called KQB198 in combination with imatinib. The goal is to determine if this combination is safe and tolerable and assess how effective the combination is at treating GIST. Imatinib has been approved by the FDA for the treatment of different types of cancer including GIST.


Eligibility

Min Age: 18 Years

Inclusion Criteria7

  • All Participants:
  • Unresectable or metastatic disease
  • Tissue confirmation of GIST
  • Valid results from local testing of blood or tumor tissue documenting the presence of a KIT mutation (must not have exon 9 mutation) or PDGFRA mutation (must not have PDGFRA D842V).
  • Measurable disease per RECIST v1.1.
  • Patients must be in 1st line of treatment for advanced or metastatic disease. Prior imatinib is allowed in adjuvant or neoadjuvant setting, as long as imatinib was stopped over 1 year ago.
  • Adequate organ function and performance status

Exclusion Criteria4

  • Participants are excluded from the study if any of the following criteria apply:
  • Unable to swallow or GI condition that prevents absorption.
  • Other active malignancies within the last 2 years.
  • History of hypersensitivity to any component of KQB198 or imatinib.

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Interventions

DRUGKQB198

Oral KQB198

DRUGImatinib (Gleevec)

Oral Imatinib


Locations(1)

Cleveland Clinic

Cleveland, Ohio, United States

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NCT07406633


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