Clinical trial · Interventional
Sequential Administration of Oral 6-Thioguanine (6-TG) After Methotrexate (MTX) in Patients With Relapsed Hodgkin's Disease (Phase II)
NCT00587873CI-TRIAL-00002376completedPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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).
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Hodgkin's Disease | Hodgkin Lymphoma | ALIAS | 0.90 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 6-Thioguanine | Drug | Thioguanine | ALIAS |
| Leucovorin calcium | Drug | Leucovorin | ALIAS |
| Methotrexate | Drug | Methotrexate | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- 1
- description
- MTX, 6-TG, and Leucovorin combination
- interventionNames
- Drug: Methotrexate
- Drug: Leucovorin calcium
- Drug: 6-Thioguanine
Primary outcomes (1)
- measure
- 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-Thioguanine (6-TG) after IV Methotrexate (MTX).
- timeFrame
- Conclusion of the study
Secondary outcomes (1)
- measure
- Define Toxicity of this sequential drug combination.
- timeFrame
- Conclusion of study
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
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.
References
Publications (0)
Data not yet available
No reference posted for this study.