Addition of Antibiotics to Upfront Treatment Regimen for Colorectal Cancer

Recruiting Phase 2 Interventional Study
Colorectal Cancer CRC
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
97 (estimated)
Sponsor
Virginia Commonwealth University · Other
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About This Trial

This is a 2-arm, noncomparative phase 2 trial designed to evaluate treatment outcomes with or without the addition of ciprofloxacin, metronidazole, and aspirin to first-line chemotherapy for patients with stage IV colorectal cancer (CRC).

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Diagnosis of stage IV colorectal cancer * Measurable disease by Response evaluation criteria in solid tumors (RECIST) 1.1 criteria * Planned first-line treatment with a 5FU-based doublet chemotherapy regimen for colon cancer, specifics of the regimen at the discretion of the t…
Contacts

Massey IIT Research Operations

804-628-6430

masseyepd@vcu.edu

CONTACT