Clinical Trials Directory

Trials / Completed

CompletedNCT02244632

Modufolin (Arfolitixorin) in Combination With 5-Fluorouracil Alone or Together With Oxaliplatin or Irinotecan in Colorectal Cancer

An Open-label, Multiple-site, Phase I/II Dose Cohort Trial of [6R] 5,10-Methylene Tetrahydrofolate (Modufolin®) in Combination With a Fixed Dose of 5-Fluorouracil (5-FU) Alone or Together With a Fixed Dose of Oxaliplatin or Irinotecan in Patients With Stage IV Colorectal Cancer

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
105 (actual)
Sponsor
Isofol Medical AB · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose is to characterise the tolerability of Modufolin (arfolitixorin) in combination with 5-FU alone, in combination with 5-FU and Oxaliplatin, in combination with 5-FU and Irinotecan and in combination with 5-FU, Oxaliplatin and Bevacizumab. Another purpose is to investigate 4 doses of Modufolin to identify the best dose for further assessment.

Detailed description

The study will investigate the tolerability of Modufolin at four (4) different dose levels (30 to 240 mg/m2) in therapy combinations with the chemotherapeutic agents 5-FU, Oxaliplatin +/- bevcizumab, and Irinotecan. When the selected phase 2 dose is determined, 40 additional patients, will be included in the study in order to acquire more data on the safety and tolerability of Modufolin at this dose level. Twenty (20) of these additional patients will be treated in with Oxaliplatin, 20 with Irinotecan.

Conditions

Interventions

TypeNameDescription
DRUGModufolin (arfolitixorin)IV injection every second week for 8 weeks.
DRUGFluorouracilIV injection every second week for 8 weeks.
DRUGOxaliplatinIV infusion every second week for 8 weeks.
DRUGIrinotecanIV infusion every second week for 8 weeks.
DRUGBevacizumabIV infusion every second week for 8 weeks.

Timeline

Start date
2014-09-01
Primary completion
2020-01-30
Completion
2020-01-30
First posted
2014-09-19
Last updated
2020-09-09

Locations

10 sites across 4 countries: Denmark, Greece, Norway, Sweden

Source: ClinicalTrials.gov record NCT02244632. Inclusion in this directory is not an endorsement.