CI

At a glance

ClinicalIndex Comparison Record
Phase 3Recruiting· 507 target
Drug / intervention
mFOLFOX6 +3 moredrug
Likely dose
mFOLFOX6 85 mgfrom record
Key inclusion· 7
  • Histologically confirmed adenocarcinoma of colon or rectum
  • Resected (R0 or R1) and/or effectively treated metastases within 3-10 weeks before randomization
  • Resected primary tumor (synchronous or metachronous)
  • No radiographic evidence of active metastatic disease at study entry on CT/MRI not older than 10 weeks prior randomization
Key exclusion· 21
  • Treatment of metastases >3 cm with radio-frequency/microwave ablation within 24 months prior to study entry
  • Treatment of metastases >5 cm with radiation (stereotactic/brachytherapy) within 24 months prior to study entry
  • NYHA Class III or greater heart failure
  • Myocardial infarction within 6 months prior to randomization

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05008809
NCT05008809Phase 3RecruitingOn TrackUpdated 6mo ago
Long Recruiting

Post-resection/Ablation Chemotherapy in Patients With Metastatic Colorectal Cancer Prospective, Randomized, Open, Multicenter Phase III Trial to Investigate the Efficacy of Active Post-resection/Ablation Therapy in Patients With Metastatic Colorectal Cancer

Dominik Paul Modest·interventional·Posted Aug 17, 2021·Updated Dec 12, 2025

In Brief

A Phase 3 clinical trial evaluating mFOLFOX6, mFOLFOXIRI, and 2 other interventions for Colorectal Cancer. Currently recruiting, targeting 507 participants across 79 sites.

Detailed Summary

This is an open-label, randomized, controlled, multicenter, phase III study with two parallel arms. Patients with metastatic colorectal cancer after definite interventional therapy of all lesions are randomized in a 2:1 fashion (favoring active therapy) to investigate the efficacy, patient reported quality of life and safety of mFOLFOXIRI/mFOLFOX-6 as additive treatment (Arm A) versus active follow-up/surveillance (Arm B).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesGermany

Timeline

Phase 3Recruiting
2022202320242025202620272028202920302031
First PostedAug 17, 2021
Enrollment StartDec 6, 2021
Primary CompletionNov 1, 2027
Study CompletionNov 1, 2030
TodayJul 2, 2026
Enrollment to primary: 5.9 yearsPosted 4.9 years agoPrimary completion in 1.3 years

Interventions

mFOLFOX6drug

Oxaliplatin: 85 mg/m², 2h IV infusion on d1 Folinic acid: 400 mg/m², 1-2 h IV infusion on d1 5-FU: (optional: 400 mg/m² bolus, 2-5 min IV infusion), 2400 mg/m², 46 h IV infusion on d1 Cycles are repeated on day 15. A total of up to 12 cycles are administered.

mFOLFOXIRIdrug

Oxaliplatin: 85 mg/m², 2h IV infusion on d1 Irinotecan: 150 mg/m², 90 min IV infusion on d1 Folinic acid: 400 mg/m², 1-2 h IV infusion on d1 5-FU: 2400 mg/m², 46 h IV infusion on d1 Cycles are repeated on day 15. A total of up to 12 cycles are administered.

FOLFIRIdrug

Folinic acid: 400mg/m², 1-2h IV Infusion on d1 5-FU: 2400 mg/m², 46 h IV infusion on d1 Irinotecan: 180 mg/m², 90-120 min IV infusion on d1 Cycles are repeated on day 15. A total of up to 12 cycles is administered.

CAPOXdrug

Capecitabine: 1000 mg/m², oral 1-0-1 on d1-14 Oxaliplatin: 130 mg/m², 3h IV infusion on d1 Cycles are repeated on day 22. A total of up to 8 cycles isadministered.