Clinical trial · Interventional
Fenretinide in Treating Patients With Recurrent or Metastatic Ovarian Epithelial or Primary Peritoneal Cancer
Phase II Trial of Fenretinide (NSC 374551) in Recurrent Ovarian Cancer and Primary Peritoneal Carcinoma
NCT00026091CI-TRIAL-00009806completedPhase 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)
Phase II trial to study the effectiveness of fenretinide in treating patients who have recurrent or metastatic ovarian epithelial or primary peritoneal cancer. Drugs used in chemotherapy, such as fenretinide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Recurrent Ovarian Epithelial Cancer | Ovarian Carcinoma | CURATED_BROADER | 0.78 |
| Recurrent Primary Peritoneal Cavity Cancer | — | UNRESOLVED | — |
| Stage IV Ovarian Epithelial Cancer | Ovarian Carcinoma | CURATED_BROADER | 0.78 |
| Stage IV Primary Peritoneal Cavity Cancer | — | UNRESOLVED | — |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| fenretinide | Drug | — | UNRESOLVED |
| laboratory biomarker analysis | Other | — | UNRESOLVED |
| pharmacological study | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Treatment (fenretinide)
- description
- Patients receive oral fenretinide twice daily on days 1-7. Treatment repeats every 21 days in the absence of disease progression or unacceptable toxicity.
- interventionNames
- Drug: fenretinide
- Other: laboratory biomarker analysis
- Other: pharmacological study
Primary outcomes (1)
- measure
- Response rate (CR or PR)
- timeFrame
- Up to 9 years
- description
- Associated exact 95% confidence intervals will be calculated.
Secondary outcomes (6)
- measure
- Time to treatment failure
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- Female
Show eligibility criteria text
Inclusion Criteria: * Patients with histologically confirmed recurrent or metastatic epithelial ovarian cancer or primary peritoneal carcinoma * Unidimensionally measurable disease; indicator lesions must not have been irradiated unless they have grown following radiation therapy * SWOG performance status 0-2 * Patients must have received a platinum and paclitaxel containing regimen * Patients are allowed to receive =\< 2 prior chemotherapy regimens for recurrent disease; patients who are rechallenged with the same chemotherapy regimen are considered to have had that regimen only once * Projected life expectancy must be at least 3 months * Signed informed consent * Absolute neutrophil count \>= 1500/ul * Platelet count \>= 100,000 ul * Bilirubin =\< 2 times the institutional limit of normal * ALT or AST =\< 3 times the upper limit of normal * Measured or calculated creatinine clearance \>= 60 ml/min * Fasting triglycerides =\< 1 time the upper limit of normal; triglycerides may be "normalized" prior to study entry with use of an antilipemic agent (atorvastatin, fenofibrate) * Patients must have recovered from acute toxicities from surgery, radiation or chemotherapy; at least 3 weeks will have elapsed since any prior therapy directed at the malignant tumor * Patients of childbearing potential must agree to use an approved method of birth control Exclusion Criteria: * Prior fenretinide is not allowed; prior 13-cis, 9-cis or all-transretinoic acid are allowed * Patients with a second malignancy within the last 5 years are not allowed, except for those with non-melanomatous skin cancer and carcinoma-in-situ of the cervix; all prior invasive malignancies must be in complete remission * The use of concomitant antioxidants, such as vitamin C or E, is not allowed * Patients with concurrent medical, psychological or social conditions of such severity that the investigator deems it unwise to enter the patient on protocol * Untreated or symptomatic brain metastases * Pregnant or nursing women
References
Publications (0)
Data not yet available
No reference posted for this study.