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) 1
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

Name
Address
City
State
Zip
Country
5777 E Mayo Blvd.
Phoenix
AZ
85054
USA
1520 San Pablo St.
Los Angeles
CA
90033
USA
2020 Santa Monica Blvd Suites 230, 580 & 600
Santa Monica
CA
90404
USA
333 Cedar St
New Haven
CT
06510
USA
Davis Building
Jacksonville
FL
32224
USA
400 S. Orange Ave.
Orlando
FL
32806
USA
5841 S. Maryland Ave
Chicago
IL
60637
USA
450 Brookline Ave
Boston
MA
02215-5450
USA
200 1st St SW
Rochester
MN
55905
USA
1275 York Ave
New York
NY
10065
USA
9500 Euclid Ave
Cleveland
OH
44195
USA
300 W. 10th Ave.
Columbus
OH
43210
USA
5115 Centre Ave,
Pittsburgh
PA
15232
USA
1515 Holcombe Blvd.
Houston
TX
77030
USA
2000 Circle of Hope
Salt Lake City
UT
84112
USA
1665 N. Ursula St.
Aurora
CO
80045
USA
1200 Medical Ctr Pkwy Suite 1200
Maumee
OH
43537
USA