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Anti-metabolites
Tas-102 for Colorectal Cancer
Phase 1
Waitlist Available
Led By Nicholas Fidelman, MD
Research Sponsored by University of California, San Francisco
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 up to 4 years
Awards & highlights
Study Summary
This study is evaluating whether a combination of a drug and a radiation therapy is safe for people with cancer.
Eligible Conditions
- Colorectal Cancer
- Colon Cancer
- Liver Metastases
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 4 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 4 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Determine dose limiting toxicities (DLT)
Maximum tolerated dose (MTD)
Secondary outcome measures
Biomarker response
Extrahepatic progression free survival (EHPFS)
Hepatic progression-free survival (HPFS)
+3 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: Tas-102 and radioembolizationExperimental Treatment2 Interventions
Combination therapy with Tas-102 and radioembolization using 90Y resin microspheres
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
SIR-Sphere
2017
Completed Phase 3
~520
Tipiracil
FDA approved
Find a Location
Who is running the clinical trial?
University of California, San FranciscoLead Sponsor
2,505 Previous Clinical Trials
15,237,534 Total Patients Enrolled
Sirtex MedicalIndustry Sponsor
28 Previous Clinical Trials
4,249 Total Patients Enrolled
Taiho Pharmaceutical Co., Ltd.Industry Sponsor
63 Previous Clinical Trials
16,277 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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