TRIAL DETAIL

Expanded Access to Bezuclastinib to be Coadministered With Sunitinib for Patients With Gastrointestinal Stromal Tumors

Drug:
Trial Name:
Expanded Access to Bezuclastinib to be Coadministered With Sunitinib for Patients With Gastrointestinal Stromal Tumors
NCT#:
Conditions:
Gastrointestinal Stromal Tumor
Status:
Recruiting
Phase:
5
Start Date 04/21/2025
Age of Trial (yrs) .4
Treatment Phase:
Gleevec-resistant
Drug Category:
KIT inhibitor
Strategy:
Block KIT
Trial Type:
Specifically GIST and only GIST
Other Protocol IDs:
CGT9486-EAP-002
Sponsor:
Cogent
Patient Contact:
Alexandra Malinowski, PharmD 1-877-633-8049 medinfo@cogentbio.com
Contact email:
Contact Phone:
Randomized:
IV or Oral:
Oral
Trial Notes:
NOTE: Must be coadministered with Sunitinib. Sunitinib is listed as "locally sourced".

Brief Summary

The purpose of this expanded access program (EAP) is to provide investigational bezuclastinib so that it can be coadministered with sunitinib to patients with a diagnosis of gastrointestinal stromal tumors (GIST) with no comparable or satisfactory alternative therapy options. The combination of bezuclastinib and sunitinib provides broad inhibition of all primary and secondary KIT mutations that commonly occur in GIST.

Eligibility Criteria
Description
Inclusion Criteria:

Able to provide written informed consent and commit to recommended EAP assessments.
≥18 years of age.
Able to swallow tablets.
Histologically confirmed locally advanced, metastatic, and/or unresectable GIST.
Intolerant to imatinib or received prior imatinib therapy for treatment of advanced, metastatic, and/or unresectable GIST that resulted in disease progression.
Meet clinically acceptable local laboratory results.
Exclusion Criteria:

Patients who are eligible for and capable of participating in and/or enrolled in an on-going bezuclastinib clinical trial.
Prior or known intolerance to sunitinib.
Patients who have previously participated in a bezuclastinib clinical trial.
Patients with persistent > Grade 2 toxicities from prior therapy.
Known PDGFR driving mutations or known SDH deficiency.
Pregnant or currently breastfeeding.
Other protocol-defined criteria apply.

Interventions

Intervention/Treatment
Drug: Bezuclastinib
Drug: Bezuclastinib

Drug: Sunitinib
Drug: Sunitinib (locally sourced)

Trial Links

Trial Results

Drug Information

Trial Sites

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