Overview

Randomized Trial of Crenolanib in Subjects With D842V Mutated GIST

Status:
Active, not recruiting
Trial end date:
2021-08-01
Target enrollment:
0
Participant gender:
All
Summary
This is a multicenter, randomized, double-blinded, placebo-controlled, trial of oral crenolanib versus oral placebo in combination with best supportive care in subjects with advanced or metastatic GIST with a D842V mutation in the PDGFRA gene. Approximately 120 subjects will be randomized in a 2:1 ratio to receive either crenolanib 100 mg or matching placebo orally (PO) 3 times daily (TID) in combination with best supportive care.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Arog Pharmaceuticals, Inc.
Collaborators:
Centre Leon Berard
Fox Chase Cancer Center
Treatments:
Crenolanib
Criteria
Inclusion Criteria:

1. Histologically or cytologically-confirmed advanced or metastatic GIST with a D842V
mutation in the PDGFRA gene as determined by central laboratory testing

2. Measurable disease as per modified RECIST 1.1

• A lesion in an area that was previously treated with local therapy (e.g. radiation,
surgery, or cryotherapy) can be considered measurable disease as long as there is
objective evidence of progression of the lesion prior to randomization

3. Subjects (male or female) ≥ 18 years of age

4. Female subjects with reproductive potential must have negative serum or urine
pregnancy test

5. Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 2

Exclusion Criteria:

1. Severe liver disease (e.g. cirrhosis, non-alcoholic steatohepatitis, sclerosing
cholangitis)

2. Known, active infection with hepatitis B virus (HBV) or hepatitis C virus (HCV)

3. Female subject who is pregnant or breastfeeding, or planning to become pregnant within
30 days after ending treatment

4. Systemic anti-cancer treatment (e.g. chemotherapy, tyrosine kinase inhibitors,
immunotherapy, or investigational agents) or investigational device within 3 weeks or
5 half-lives (if the drug's half-life in subject is known) prior to randomization,
whichever is shorter