Expired Study
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New York, New York 10065


The objective of this study is to determine the incidence of complete and partial response and the duration of response in patients with recurrent or resistant Hodgkin's disease (HD) treated with sequential administration of oral 6-Thioguanin (6-TG) after IV Methotrexate (MTX).


Inclusion Criteria: - Patients with histologic proof of HD who are in relapse and have failed > or = to 2 prior chemotherapy regimens. - Patients must have a life expectancy of at least 8 weeks. - All patients must have ECOG performance level rating of < or = to 2. - Patients or their parents (guardian) must sign an informed consent indicating that they are aware of the investigational nature of the study. - Patients must have recovered from the toxic effects of prior therapy before entering this study or at least 2 weeks should have elapsed since the end of last course of CT. - Patients must have adequate liver function (bilirubin < or = to 2.0 mg/dl, SGOT less than 1.5 times normal (unless it is due to disease), adequate renal function (creatinine < or = to 1.5 mg/dl, creatinine clearance > or = to 60 ml/min/1.73 m2). - Patients should have a granulocyte count > or = to 500/gL and a platelet count > or = to 100,000/uL (unless due to disease involvement of the bone marrow). - Male and female patients of child-bearing age should use effective methods of contraception, if sexually active. Exclusion Criteria: - Patients with active infections or significant medical conditions other than their malignancy shall be excluded. - Patients with HD who had prior MTX or 6-TG should be excluded.



Primary Contact:

Principal Investigator
Tanya Trippett, MD
Memorial Sloan-Kettering Cancer Center/94-030

Backup Contact:


Location Contact:

New York, New York 10065
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: February 04, 2019

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