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 @ 4:41 PM
Ignite Modification Date:
2025-12-24 @ 4:41 PM
NCT ID:
NCT00085566
Eligibility Criteria:
DISEASE CHARACTERISTICS:
* Histologically confirmed diagnosis of 1 of the following:
* Glioblastoma multiforme (GBM) (phase I only)
* Progressive disease despite standard therapy
* Progressive disease based on 1 of the following:
* New or progressive (25% bidimensional increase) soft tissue masses on CT scan or MRI
* New or prior lesions that have increased in size by physical examination
* Patients who had prior interstitial brachytherapy or stereotactic radiosurgery must have confirmation of true disease progression (rather than radiation necrosis) by positron-emission tomography scan, thallium scanning, magnetic resonance spectroscopy, or surgical documentation
* Castrate metastatic prostate cancer (closed to accrual as of 10/19/2006) (phase I and II)
* Progressive disease despite standard therapy AND castrate levels \< 50 ng/dL of testosterone
* Progressive disease based on 1 or more of the following:
* A minimum of 3 rising levels of prostate-specific antigen (PSA) that are obtained 1 or more weeks apart OR 2 rising PSA values obtained more than 1 month apart with at least a 25% increase over the range of values
* New or progressive (25% bidimensional increase) soft tissue masses on CT scan or MRI
* New metastatic lesions
* Patients on an antiandrogen as part of initial therapy must show disease progression after discontinuation of the antiandrogen
* Patients who have not undergone surgical orchiectomy must continue with medical therapy (e.g., gonadotropin-releasing hormone analogs) to maintain castrate levels of serum testosterone
* No brain metastases
PATIENT CHARACTERISTICS:
Age
* Over 18
Performance status
* Karnofsky 70-100%
Life expectancy
* More than 3 months
Hematopoietic
* Absolute neutrophil count ≥ 1,500/mm\^3
* Platelet count ≥ 100,000/mm\^3
* WBC ≥ 3,000/mm\^3
Hepatic
* ALT and AST ≤ 2.5 times upper limit of normal (ULN)
* Bilirubin ≤ 1.5 mg/dL
Renal
* Creatinine within 1.5 times ULN (\< 1.95 mg/dL at MSKCC)
Cardiovascular
* No significant cardiovascular disease
* No congestive heart failure
* No New York Heart Association class III or IV cardiac disease
* No active angina pectoris
* No myocardial infarction within the past 6 months
Other
* Not pregnant
* Negative pregnancy test
* Fertile patients must use effective contraception
* No serious medical illness
* No severe infection
* No severe malnutrition
* No other active malignancy except non-melanoma skin cancer
* Patients are not considered to have an active malignancy if they have completed prior therapy and currently have a \< 30% risk for relapse
PRIOR CONCURRENT THERAPY:
Biologic therapy
* No concurrent biological therapy
* No concurrent immunotherapy
Chemotherapy
* No concurrent chemotherapy
Endocrine therapy
* See Disease Characteristics
Radiotherapy
* See Disease Characteristics
* More than 4 weeks since prior radiotherapy
* No concurrent radiotherapy
Surgery
* See Disease Characteristics
* Prior recent resection of recurrent or progressive GBM allowed provided patient has recovered
* More than 4 weeks since prior major surgery
Other
* Recovered from all prior therapy
* More than 4 weeks since prior investigational anticancer drugs
* No concurrent anticonvulsant that interacts with CYP3A4 (e.g., phenytoin, carbamazepine, or phenobarbital)
* No other concurrent cytotoxic therapy
* No other concurrent investigational or commercial agents or therapies for the malignancy
Healthy Volunteers:
False
Sex:
MALE
Minimum Age:
18 Years
Maximum Age:
120 Years
Study:
NCT00085566
Study Brief:
Protocol Section:
NCT00085566