Clinical trial · Interventional
Myocet ® - Carboplatine in Ovarian Cancer in Relapse, Sensitive to the Platinum
Phase Ib / II Trial Evaluating the Association Myocet ® - Carboplatine in Patients Having a Cancer of the Ovary in Relapse, Sensitive to the Platinum
NCT01705158CI-TRIAL-00069348MYCAcompletedPhase 1 / Phase 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)
The purpose of this study is to determine the efficacy and the safety of the association of carboplatine and liposomal doxorubicin in patient with ovarian cancer in relapse, sensitive to platin.
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 |
|---|---|---|---|
| Ovarian Cancer | Malignant Ovarian Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| carboplatin and liposomal doxorubicin | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- carboplatin and liposomal doxorubicin
- description
- carboplatin and liposomal doxorubicin in ovarian cancer in realapse
- interventionNames
- Drug: carboplatin and liposomal doxorubicin
Primary outcomes (1)
- measure
- Determine the control disease rate in 1 year
- timeFrame
- 12 months
- description
- To determine the proportion of not progressive patients in 1 year (rate of control of the disease or the rate of not progress in 12 months)
Secondary outcomes (1)
- measure
- To estimate the rate of objective answer (CR/PR)
- timeFrame
- 2,5 years
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * First or second relapse of a carcinoma of the ovary, the fallopian tubes or the peritoneal tissue histological proved. * Interval without progress \> 6 months after the last administration of a salt of platinum(deck). * Measurable Disease (according to the criteria RECIST 1.1) or an assessable disease according to CA-125 (according to the criteria of the GCIG). * Satisfactory biological Balance sheet(Assessment), according to the following criteria: * Neutrophiles \> 1,5x 109/L, Plaques \> 100 x 109/L, Haemoglobin \> 9,0 g/dL. * Bilirubine \< 1.5 x LSN (Normal Superior Limit), transaminases and alkaline phosphatase \< 2. 5 x LSN. * Creatinin clearance \> 50 mL/min calculated according to the formula of Cockroft-Gault or MDRD. * Performance status \< 2. * Life expectancy of at least 12 weeks. * Age \> 18 years. * Capacity to follow the protocol. * Consent signed before any procedure of inclusion. * Membership in a national insurance scheme. Exclusion Criteria: * Tumor of mild histology or borderline, or malignant not epithelial tumor of the ovary, the fallopian tubes or the peritoneal tissue(eg. tumor of germ cells, tumor of the sexual cords and the stroma). * History of abdominal or pelvic radiotherapy. * Patient having received more than 2 lines of chemotherapy. * Patient in 3rd relapse or more. * History of another malignant tumor during the last 5 years, with the exception of a carcinoma in situ by the neck of the womb or by a squamous-cell carcinoma of the skin treated in a adequate way or any solid tumor considered in forgiveness completes without relapse for at least 5 years. * Patients having a stubborn illness in the platinum, (eg. progress during the last chemotherapy or in 6 months following the last administration of platinum). * Occlusive or sub-occlusive disease or presence of symptomatic intellectual metastases. * Heart disorder dissuading the use of an anthracycline. * Left venticular ejection fraction (LVEF) defined by MUGA/ECHO \< 50%. * Wait presenting a severe infection. * Woman old enough to procreate not using adequate contraceptive method. * Concomitant disease not allowing a surgery and/or a chemotherapy. * Pathology severe or concomitant not compatible with the taking of the study treatment or the participation of the patient in the study.
References
Publications (1)
- DERIVEDRomeo C, Joly F, Ray-Coquard I, El Kouri C, Mercier-Blas A, Berton-Rigaud D, Kalbacher E, Cojocarasu O, Fabbro M, Cretin J, Zannetti A, Abadie-Lacourtoisie S, Mollon D, Hardy-Bessard AC, Provansal M, Blot E, Delbaldo C, Lesoin A, Freyer G, You B. Non-pegylated liposomal doxorubicin (NPLD, Myocet(R)) + carboplatin in patients with platinum sensitive ovarian cancers: A ARCAGY-GINECO phase IB-II trial. Gynecol Oncol. 2019 Jan;152(1):68-75. doi: 10.1016/j.ygyno.2018.10.043. Epub 2018 Nov 14. PMID 30446275