Clinical trial · Interventional
Metformin for the Treatment of mCRC Patients Undergoing FOLFIRI Plus Target Therapy
Metformin as an Adjunctive Therapy for the Treatment of Metastatic Colorectal Cancer Patients Undergoing FOLFIRI Plus Target Therapy
NCT06826092CI-TRIAL-00085977recruitingPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
To investigate progression-free survival (PFS) in patients with metastatic colorectal cancer treated with chemotherapy FOLFIRI monotherapy or chemotherapy FOLFIRI combined with Metformin
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Progression-Free Survival | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| FOLFIRI plus target therapy only | Drug | — | UNRESOLVED |
| Metformin Pill | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Study group
- description
- Metformin 500mg TID、FOLFIRI (Leucovorin 200 mg/m2、5-FU 2800 mg/m2、Irinotecan 180 mg/m2) plus target therapy
- interventionNames
- Drug: Metformin Pill
- type
- PLACEBO_COMPARATOR
- label
- Control group
- description
- FOLFIRI (Leucovorin (LV), 200 mg/m2, 2-hour infusion, 5-FU, 2,800 mg/m2, 46-hour infusion, Irinotecan (IRI), 180 mg/m2, 2-hour infusion) plus target therapy
- interventionNames
- Drug: FOLFIRI plus target therapy only
Primary outcomes (1)
- measure
- Disease progression-free survival (PFS)
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 20 Years
- Maximum age
- 90 Years
Show eligibility criteria text
Inclusion Criteria: 1. Aged between 20 and 90 years old 2. Patients diagnosed with metastatic colorectal cancer who is going to receive FOLFIRI chemotherapy 3. Female must not be planning to become pregnant or breastfeeding, and not pregnant at any point during treatment. (Contraception is required to participate in this trial) 4. Those without major physiological diseases (example of major cardiovascular disease is acute myocardial infarction; example of major cerebrovascular disease is acute stroke, malignant hypertension, acute kidney failure, acute liver failure) 5. Those who are not allergic to the relevant drugs required for the test 6. Those who can follow the doctor's order to take the medicine 7. Subjects must be willing to sign the consent form 8. Blood sugar level above 80 mg/dL Exclusion Criteria: Subjects who meet any of the following exclusion conditions are not allowed to join the trial 1. Patients other than the above-mentioned main inclusion criteria. 2. Non-native speakers 3. Known allergy to metformin or any of its components. 4. Severe instability in diabetes (ketoacidosis). 5. Blood sugar level lower than 80 mg/dL 6. Heart failure, respiratory insufficiency. 7. inadequate hematopoietic function defined as below: * hemoglobin \< 9 g/dL; * absolute neutrophil count (ANC) \< 1,500/mm3; * platelet count \< 100,000/mm3; 8. inadequate organ functions defined as below: * total bilirubin \> 2 times upper limit of normal (ULN); * hepatic transaminases (ALT and AST) \> 2.5 x ULN; * creatinine \> 1.5 x ULN;
References
Publications (0)
Data not yet available
No reference posted for this study.