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Alkylating Agent
rebastinib for Solid Tumors
Phase 1 & 2
Waitlist Available
Research Sponsored by Deciphera Pharmaceuticals LLC
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up approximately 24 months
Awards & highlights
Study Summary
This trial is testing a new cancer drug, rebastinib, to see if it is safe and works well with carboplatin to treat solid tumors.
Eligible Conditions
- Solid Tumors
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ approximately 24 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~approximately 24 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Adverse Events (Part 1 and Part 2)
Objective response rate (ORR) (Part 2)
Secondary outcome measures
Area under the concentration-time curve (AUC) of rebastinib
Duration of response (DOR)
Maximum observed concentration (Cmax) of rebastinib
+3 moreTrial Design
2Treatment groups
Experimental Treatment
Group I: Part 2Experimental Treatment2 Interventions
Dose expansion in the following tumor types at the recommended Phase 2 dose (RP2D) of rebastinib in combination with carboplatin
Triple-negative breast cancer
Platinum-sensitive Ovarian cancer
Mesothelioma
Group II: Part 1Experimental Treatment2 Interventions
Dose comparison between 50 or 100 mg BID of rebastinib orally (PO) dosed in 21-day cycles in combination with carboplatin administered by IV infusion at either AUC5 or AUC6 once every 3 weeks
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Rebastinib
Not yet FDA approved
Carboplatin
FDA approved
Find a Location
Who is running the clinical trial?
Deciphera Pharmaceuticals LLCLead Sponsor
16 Previous Clinical Trials
2,127 Total Patients Enrolled
Frequently Asked Questions
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