Phase 2 Trial Using Talampanel in Patients With Recurrent High Grade Gliomas

NCT ID: NCT00062504

Last Updated: 2011-05-23

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2003-07-31
• Study Completion Date: 2006-04-30

Brief Summary

To analyze the effect of Talampanel on progression free survival in patients with recurrent high grade gliomas.

Detailed Description

To determine the efficacy of Talampanel in patients with recurrent malignant glioma as measured by 6-month progression survival, as well as to obtain preliminary information regarding the spectrum of toxicities of the drug among this patient population.

Conditions

Glioblastoma Multiforme; Anaplastic Astrocytoma; Anaplastic Oligodendroglioma; Anaplastic Mixed Oligoastrocytoma

Study Design

• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT

Study Groups

1

Valproic: 10mg TID week 1, 25mg TID week 2, 35mg week 3

Group Type: EXPERIMENTAL

Talampanel

Intervention Type: DRUG

10mg, 25 mg, 35 mg, 50 mg, 75mg TID for 3 weeks

2

Non-enzyme-inducing anti-epileptic drugs: 25mg TID week 1, 35mg week 2, 50mg week 3

Group Type: EXPERIMENTAL

Talampanel

Intervention Type: DRUG

10mg, 25 mg, 35 mg, 50 mg, 75mg TID for 3 weeks

3

Enzyme-inducing anti-epileptic drugs: 35mg TID week 1, 505mg week 2, 75mg week 3

Group Type: EXPERIMENTAL

Talampanel

Intervention Type: DRUG

10mg, 25 mg, 35 mg, 50 mg, 75mg TID for 3 weeks

Interventions

Talampanel

10mg, 25 mg, 35 mg, 50 mg, 75mg TID for 3 weeks

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Patients with histologically proven intracranial malignant glioma will be eligible for this protocol. Malignant glioma include glioblastoma multiforme (GBM), anaplastic astrocytoma (AA), anaplastic oligodendroglioma (AO), anaplastic mixed oligoastrocytoma (AMO), or malignant astrocytoma NOS (not otherwise specified).

2. Patients must have unequivocal evidence for tumor progression by MRI or CT scan. This scan should be performed within 14 days prior to registration and on a steroid dosage that has been stable for at least 5 days.

3. Patients having undergone recent resection of recurrent or progressive tumor will be eligible as long as all of the following conditions apply:

1. They have recovered from the effects of surgery.

2. Residual disease following resection of recurrent tumor is not mandated for eligibility into the study. To best assess the extent of residual disease post-operatively, a CT/ MRI should be done:

• no later than 96 hours in the immediate post-operative period or
• at least 4 weeks post-operatively, and
• within 14 days of registration, and
• on a steroid dosage that has been stable for at least 5 days.

4. If the 96-hour scan is more than 21 days before registration, the scan needs to be repeated.

5. Patients must have failed prior radiation therapy and must have an interval of greater than or equal to 4 weeks from the completion of radiation therapy to study entry.

6. All patients must sign an informed consent indicating that they are aware of the investigational nature of this study.

7. Patients must be > 18 years old, and with a life expectancy > 8 weeks.

8. Patients must have a Karnofsky performance status of > 60.

9. Patients must have recovered from the toxic effects of prior therapy: 4 weeks from any investigational agent, 4 weeks from prior cytotoxic therapy, two weeks from vincristine, 6 weeks from nitrosoureas, 3 weeks from procarbazine administration, and 1 week for non-cytotoxic agents, e.g., interferon, tamoxifen, thalidomide, cis-retinoic acid, etc. (radiosensitizer does not count).

10. Patients must have adequate bone marrow function (ANC > 1,200/mm3, platelet count of > 100,000/mm3, and hemoglobin > 10 gm/dl), adequate liver function (SGOT and bilirubin < 2 times ULN), and adequate renal function (serum creatinine < 1.5 mg/dL otherwise a measured 24-hour creatinine clearance > 60 cc/min) before starting therapy. These tests must be performed within 14 days prior to registration.

11. Patients must not have any significant medical illnesses that in the investigator's opinion cannot be adequately controlled with appropriate therapy or would compromise the patients' ability to tolerate this therapy.

12. This study was designed to include women and minorities, but was not designed to measure differences of intervention effects.

13. Patients must not have active infection requiring IV antibiotics.

14. Patients must not be pregnant or nursing, and all patients (both men and women) must be willing to practice birth control during and for 2 months after treatment with Talampanel. Women of childbearing potential (WCBP) must have a negative serum or urine pregnancy test. In addition, sexually active WCBP must agree to use adequate contraceptive methods (oral, injectable, or implantable hormonal contraceptive; tubal ligation; intra-uterine device; barrier contraceptive with spermicide; or vasectomized partner).

Exclusion Criteria

1. Patients who, in the view of the treating physician, have significant active cardiac, hepatic, renal, or psychiatric diseases are ineligible that would significantly increase the risk of using talampanel.

2. No concurrent use of other standard chemotherapeutics or investigative agents.

3. Patients known to have an active, life-threatening malignancy.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: collaborator

Teva Branded Pharmaceutical Products R&D, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Teva Neuroscience

Other Identifiers

IXR-205-21-189

Identifier Type: -

Identifier Source: org_study_id