Second-Line Therapy Study For Potentially Platinum-Sensitive Relapsed Ovarian Cancer

Inclusion criteria:

   - Subject must have baseline laboratory values as follows:

   - Hemoglobin 9.0 g/dL

   - Neutrophils 1,500/mm3

   - Platelets 100,000/mm3

   - Creatinine 1.5 mg/dL ( 133 mol/l) or creatinine clearance 60 mL/min

   - Serum bilirubin < 2.0 mg/dL (< 35 umol/L)

   - SGOT/AST, SGPT/ALT and alkaline phosphatase < 2 times ULN if liver metastases are
   absent by abdominal CT or MRI or < 5 times ULN if liver metastases are present

   - Subject is allowed to have received, but is not required to have received, one
   additional prior non-cytotoxic regimen for management of recurrent or persistent
   disease according to the following definition: Non-cytotoxic (biologic or cytostatic)
   agents include (but are not limited to) monoclonal antibodies, cytokines, and
   small-molecule inhibitors of signal transduction

   - Subject is female 18 years of age with an ECOG Performance Status of 0, 1 or 2

   - Subject has recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer
   which was histologically confirmed at the time of the primary diagnosis

   - Subject has received one prior platinum-based chemotherapeutic regimen (containing
   either carboplatin or cisplatin) for the treatment of primary disease. Consolidation
   chemotherapy is not permitted

   - Subject's disease is considered potentially platinum-sensitive (i.e., have had a
   platinum-free interval following complete response to carboplatin or cisplatin of
   greater than 6 months)

   - Subject must have at least one measurable lesion as determined by diagnostic studies
   including CT or MRI or physical exam. Measurable disease must be accurately measured
   in at least one dimension (longest dimension to be recorded). Each lesion must be 20
   mm in their longest dimension when measured by conventional techniques, including
   palpation, plain X-ray, CT and MRI, or 10 mm when measured by spiral CT. Palpable
   tumor masses that cannot be evaluated radiologically must have 2 diameters 20 mm. An
   attempt to document lesion size by ultrasound should be undertaken for palpable
   lesions not visualized on CT (or MRI).

   - The same diagnostic imaging method used to evaluate disease must be used throughout
   the study to evaluate lesions consistently

   - Stable blood, liver and renal functions.

   - Subjects of child-bearing potential must be practicing adequate contraception (e.g.
   oral contraceptives, diaphragm plus spermicide, or IUD) for at least 3 months prior to
   study start. The same contraceptive method should be used throughout the study and
   continue for at least 4 weeks after the end of the study

Exclusion criteria:

   - Pregnant or lactating.

   - Subject has received more than 1 prior chemotherapy regimen or a history of
   consolidation cytotoxic chemotherapy

   - Subject has concomitant or history of previous malignancies, with the exception of
   adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer,
   or other cancer from which the subject has been disease-free for 5 years

   - Subject has brain metastases as documented by CT or MRI. Note: Asymptomatic subjects
   do not require CT or MRI to rule out brain metastases

   - Received previous treatment with HYCAMTIN.

   - Subject has received an investigational agent within 30 days or 5 half-lives
   (whichever is longer) prior to study entry

   - Received prior radiation therapy for ovarian cancer