Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Durham, North Carolina 27710


Purpose:

Objectives: - To determine the maximum tolerated dose of oral topotecan when administered with Temodar to patients with malignant glioma - To characterize any toxicity associated with the combination oral topotecan and Temodar. - To observe patients for clinical antitumor response when treated with oral topotecan and Temodar.


Study summary:

Subjects are patients with glioblastoma (GBM), anaplastic astrocytoma (AA) or grade 3 or greater WHO astrocytic, oligodendroglial or mixed glial tumors, which were initially diagnosed by histologic examination of biopsy/resection. Modified classical "3+3" phase I design used to determine maximum tolerated dose of topotecan in combination with Temodar.


Criteria:

Inclusion Criteria: - Histology: GBM, AA or grade 3 or greater WHO astrocytic, oligodendroglial or mixed glial tumors which were initially diagnosed by histologic exam of biopsy/resection - Age: > or equal to 18 years - Performance Status: Karnofsky Performance Status > or equal to 60% at study entry. - Renal Function: Serum creatinine < 1.5 mg/dl or creatinine clearance > 60 ml/dL. - Hematologic Status: The following baseline studies will be required before entry: total granulocyte count > or equal to 1000/microliter; platelet count > 100,000/microliter - Hepatic Function: Serum SGOT & total bilirubin < or equal to 2.5 times ULN. - Note: All lab parameters must have been obtained within 1 week of registration - Consent: Signed informed consent, approved by IRB, will be obtained prior to initiating treatment - Corticosteroids: For patients currently on corticosteroids, patients should be on stable dose for 1 week prior to study entry, if clinically possible. - Prior Therapy: Interval of at least 2 weeks between prior surgical resection or prior radiotherapy (XRT) or 1 week from completion of chemotherapy and all toxicities are < or equal to grade 1 & enrollment on this protocol unless there is unequivocal evidence of progressive disease. - Patients with Reproductive Potential: Patients must agree to practice effective birth control measures while on study and for 2 months after completing therapy Exclusion Criteria: - Pregnant or breast feeding women or women or men with reproductive potential not practicing adequate contraception. This therapy may be associated with potential toxicity to the fetus or child that exceeds minimum risks necessary to meet health needs of mother - Active infection requiring intravenous antibiotics - Prior failure with either topotecan or temozolomide


NCT ID:

NCT00610571


Primary Contact:

Principal Investigator
Katherine B Peters, MD, PhD
Duke University Health System


Backup Contact:

N/A


Location Contact:

Durham, North Carolina 27710
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 22, 2018

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.