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Anti-metabolites
IXO regimen for Colorectal Cancer (IXOr Trial)
Phase 2
Waitlist Available
Led By Derek Jonker, MD
Research Sponsored by Ottawa Hospital Research Institute
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 q6 months first 2 years and annually thereafter
Awards & highlights
IXOr Trial Summary
This is a prospective open label single-arm, single-institution phase II clinical trial to test the efficacy of neoadjuvant treatment with IXO (Irinotecan, Capecitabine [Xeloda], Oxaliplatin) followed by chemoradiotherapy and resection in patients with resectable non-metastatic primary rectal cancer of stage cT3-T4 N0-N2.
Eligible Conditions
- Colorectal Cancer
IXOr Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ q6 months first 2 years and annually thereafter
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~q6 months first 2 years and annually thereafter
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Pathological complete response (pCR)
Secondary outcome measures
Number of Participants with Adverse Events as a Measure of Safety and Tolerability
OS
Objective Response
+5 moreIXOr Trial Design
1Treatment groups
Experimental Treatment
Group I: IXO regimenExperimental Treatment1 Intervention
single-group
Find a Location
Who is running the clinical trial?
Ottawa Hospital Research InstituteLead Sponsor
561 Previous Clinical Trials
2,785,676 Total Patients Enrolled
Ottawa Regional Cancer FoundationUNKNOWN
1 Previous Clinical Trials
23 Total Patients Enrolled
SanofiIndustry Sponsor
2,164 Previous Clinical Trials
3,514,965 Total Patients Enrolled
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