Clinical trial · Interventional
Study of Metformin With Carboplatin/Paclitaxel Chemotherapy in Patients With Advanced Ovarian Cancer
Phase Ib Study of Metformin in Combination With Carboplatin/Paclitaxel Chemotherapy in Patients With Advanced Ovarian Cancer
NCT02312661CI-TRIAL-00076769OVMETcompletedPhase 1ClinicalTrials.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)
Molecularly targeted agents which inhibit the mammalian target of rapamycin (mTOR) pathway and/or circumvent p53 in the induction of apoptosis are exciting potential targets in ovarian cancer. Metformin is a biguanide, widely used in the treatment of type 2 diabetes mellitus, that has shown anti-cancer activity in preclinical studies. The main mechanism of metformin's effect is mTOR pathway inhibition and, in addition, it has been shown to circumvent p53-induced apoptosis making it an exciting, potentially effective drug in ovarian cancer.
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 |
|---|---|---|---|
| Epithelial Ovarian Cancer | Ovarian Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Carboplatin | Drug | Carboplatin | ALIAS |
| Metformin | Drug | Metformin | ALIAS |
| Paclitaxel | Drug | Paclitaxel | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Carboplatin / paclitaxel /metformin
- description
- Three-weekly cycles of carboplatin/paclitaxel chemotherapy in combination with metformin treatment
- interventionNames
- Drug: Metformin
- Drug: Carboplatin
- Drug: Paclitaxel
Primary outcomes (1)
- measure
- Number of participants with Adverse Events as a measure of safety and tolerability
- timeFrame
- 1-2 years
- description
- Data will be used to determine recommended phase 2 dose
Secondary outcomes (1)
- measure
- Pharmacokinetics (AUC, Tmax,Cmax) of carboplatin and paclitaxel chemotherapie
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patients with advanced stage (FIGO III-IV), histologically confirmed and documented epithelial ovarian carcinoma * Patients eligible for neo-adjuvant carboplatin/paclitaxel chemotherapy prior to surgical debulking OR patients with relapsed or progressive ovarian cancer after initial treatment eligible for palliative carboplatin/paclitaxel chemotherapy * Eastern Cooperative Oncology Group-performance status (ECOG-PS) of 0-2 * Age ≥ 18 years * Laboratory Requirements - within 7 days prior to enrolment: * absolute neutrophil count (ANC) ≥1.5 x 109/L * platelets \> 100 x 109/L * hemoglobin \>9g/dl. Patients may be transfused or use erythropoietin to maintain hemoglobin values ≥ 9 g/dl. * hepatic function: bilirubin ≤1.5×upper limit of normal (ULN), aspartate aminotransferase (AST)/ALT≤2.5×ULN * estimated creatinine clearance ≥ 60ml/min * Before patient registration/randomization, written informed consent for the trial must be given according to International Conference on Harmonisation (ICH)/ good clinical practice (GCP), and national/local regulations. Exclusion Criteria: * Current or recent (within 30 days of first study dosing) treatment with another investigational drug or participation in another investigational study. * Metformin within 4 weeks prior to enrolment. * Symptomatic central nervous system (CNS) metastasis * Pre-existing peripheral neuropathy ≥ Common toxicity criteria (CTC) grade 2. * Pregnant or lactating females. Serum pregnancy test to be assessed within 7 days prior to study treatment start, or within 14 days with a confirmatory urine pregnancy test within 7 days prior to study treatment start. * Women of childbearing potential (defined as \<2 years after last menstruation and not surgically sterile) not using effective, non-hormonal means of contraception (intrauterine contraceptive device, barrier method of contraception in conjunction with spermicidal jelly) during the study and for 6 months after the last study medication. * Known hypersensitivity to any of the study drugs or excipients. * Serious active infection requiring i.v. antibiotics at enrolment. * Unstable medical conditions. * Evidence of any other medical conditions, physical examination or laboratory findings that may interfere with the planned treatment, affect patient compliance or place the patient at high risk from treatment related complications.
References
Publications (0)
Data not yet available
No reference posted for this study.