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Phase II Study of Liposomal Irinotecan With TAS102 and Bevacizumab for Patients With Metastatic Colorectal Cancer

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This study is being done to see if combining liposomal irinotecan with TAS102 and bevacizumab confers clinical benefit for patients with treatment refractory metastatic colorectal cancer.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients must be ≥ 18 years of age

• Eastern Cooperative Oncology Group (ECOG) performance must be 0 or 1.

• Patients must have a histologically or cytologically confirmed diagnosis of colorectal adenocarcinoma and be metastatic or unresectable.

• The cancer must be mismatch repair proficient.

• Patients must have had prior treatment with 5-fluorouracil, oxaliplatin, irinotecan containing regimens. If RAS wild-type must have received prior anti-EGFR therapy with either cetuximab or panitumumab. If RAS wild-type and HER2 positive then must have had a prior HER2 targeted therapy.

Locations
United States
Wisconsin
University of Wisconsin Carbone Cancer Center
RECRUITING
Madison
Contact Information
Primary
Cancer Connect
clinicaltrials@cancer.wisc.edu
800-622-8922
Time Frame
Start Date: 2023-10-13
Estimated Completion Date: 2028-07
Participants
Target number of participants: 50
Treatments
Experimental: Participants with Metastatic or Unresectable Colorectal Cancer
Male and females aged 18 years and older with histologically confirmed metastatic or unresectable (not amenable to curative therapy) colorectal cancer.
Related Therapeutic Areas
Sponsors
Collaborators: Ipsen
Leads: University of Wisconsin, Madison

This content was sourced from clinicaltrials.gov