Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 1:12 PM
Ignite Modification Date:
2025-12-24 @ 1:12 PM
NCT ID:
NCT00091195
Eligibility Criteria:
Inclusion Criteria:
* Histologically or cytologically confirmed primary ovarian epithelial or peritoneal cavity cancer
* Histologic confirmation of recurrent disease not required
* Measurable disease, defined as ≥ 1 unidimensionally measurable lesion ≥ 20 mm by conventional techniques (including palpation, plain x-ray, computed tomography \[CT\] scan, or magnetic resonance imaging \[MRI\]) OR ≥ 10 mm by spiral CT scan
* Achieved a complete response after initial prior platinum-containing (cisplatin or carboplatin) chemotherapy regimen (e.g., conventional-dose therapy, high-dose therapy, consolidation therapy, or extended therapy after surgical or nonsurgical assessment)
* Patients who have not received paclitaxel or docetaxel as initial therapy may receive a second regimen containing these drugs
* No prior chemotherapy for persistent or recurrent disease, including re-treatment with the original regimen
* Platinum-sensitive disease, defined as having a treatment-free interval with no evidence of progressive disease for \> 6 but \< 12 months after completion of a platinum-based regimen
* No known brain metastases
* Performance status - Eastern Cooperative Oncology Group (ECOG) 0-2
* Performance status - Karnofsky 60-100%
* More than 6 months
* White blood cells (WBC) ≥ 3,000/mm\^3
* Absolute neutrophil count ≥ 1,500/mm\^3
* Platelet count ≥ 100,000/mm\^3
* Bilirubin normal
* Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 times upper limit of normal (ULN)
* Creatinine ≤ 1.5 times ULN
* Creatinine clearance ≥ 60 mL/min
* No New York Heart Association class III or IV congestive heart failure
* No myocardial infarction within the past year
* No uncontrolled dysrhythmias
* No poorly controlled angina
* No history of serious ventricular arrhythmia (e.g., ventricular tachycardia or ventricular fibrillation, ≥ 3 beats in a row)
* QTc interval \< 500 msec
* No other significant cardiac disease
* Potassium normal
* Magnesium normal
* No uncontrolled electrolyte abnormality (hypokalemia and hypomagnesemia)
* No ongoing or active infection requiring antibiotics
* No history of allergic reactions attributed to compounds of similar chemical or biological composition to study drug
* No neuropathy ≥ grade 2
* No other uncontrolled illness
* No psychiatric illness or social situation that would preclude study compliance
* No other invasive malignancy within the past 5 years except nonmelanoma skin cancer
* Not pregnant or nursing
* Negative pregnancy test
* Fertile patients must use effective contraception
* No prior monoclonal antibodies, cytokines, or signal transduction inhibitors for recurrent disease
* No concurrent biologic therapy
* See Disease Characteristics
* More than 4 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin) for the primary malignancy
* No prior FR901228 (depsipeptide)
* No other concurrent chemotherapy
* More than 4 weeks since prior hormonal therapy for the primary malignancy
* Concurrent estrogen replacement therapy allowed
* More than 4 weeks since prior radiotherapy
* No prior radiotherapy to \> 25% of bone marrow
* No concurrent radiotherapy
* Recovered from all prior therapy
* More than 4 weeks since prior noncytotoxic therapy for the primary malignancy
* No other prior noncytotoxic therapy for recurrent disease
* No concurrent combination anti-retroviral therapy for HIV-positive patients
* No other concurrent drugs known to have histone deacetylase inhibitor activity (e.g., valproic acid)
* No concurrent agents that cause QTc prolongation
* No other concurrent investigational agents
* No other concurrent anticancer agents
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT00091195
Study Brief:
Protocol Section:
NCT00091195