Clinical trial · Interventional
Interleukin-2 in Treating Patients With Myelodysplastic Syndrome
A PHASE I TRIAL OF SUBCUTANEOUS, OUTPATIENT INTERLEUKIN-2 FOR PATIENTS WITH MYELODYSPLASTIC SYNDROME (MDS)
NCT00002746CI-TRIAL-00037333completedPhase 1ClinicalTrials.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)
RATIONALE: Interleukin-2 may stimulate a person's white blood cells to kill cancer cells. PURPOSE: Phase I trial to study the effectiveness of interleukin-2 in treating patients with myelodysplastic syndrome.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Leukemia | Leukemia | ONTOLOGY_EXACT | 0.90 |
| Myelodysplastic/Myeloproliferative Neoplasms | Myelodysplastic/Myeloproliferative Neoplasm | CURATED_BROADER | 0.80 |
| Myelodysplastic Syndromes | Myelodysplastic Syndrome | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| aldesleukin | Biological | Aldesleukin | ALIAS |
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 15 Years
- Maximum age
- 120 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS: * Histologically confirmed myelodysplastic syndrome: Refractory anemia (RA), refractory anemia with ringed sideroblasts (RARS), refractory anemia with excess blasts (RAEB) or chronic myelomonocytic leukemia (CMML) * No patients with refractory anemia with excess blasts in transformation (RAEB-t) PATIENT CHARACTERISTICS: Age: * 15 and over Performance status: * Karnofsky 70-100 Hematopoietic: * Platelet count greater than 20,000 Hepatic: * Bilirubin less than 1.6 mg/dL * SGOT less than 150 U/L Renal: * Creatinine no greater than 2.0 mg/dL Cardiovascular: * No symptoms of coronary artery disease, congestive heart failure, edema, clinically manifest hypotension, presence of cardiac arrhythmias on EKG, or severe hypertension Pulmonary: * No significant pleural effusion, dyspnea at rest or severe exertional dyspnea Other: * No patients with nephrotic syndrome * No uncontrolled infections or active peptic ulcer disease * No serious intercurrent medical illness * Not pregnant or nursing * Adequate contraception required of all patients PRIOR CONCURRENT THERAPY: Biologic therapy: * At least 4 weeks since prior immunosuppressive therapy Chemotherapy: * At least 4 weeks since prior chemotherapy Endocrine therapy: * At least 2 weeks since corticosteroid therapy * At least 4 weeks since other endocrine therapy Radiotherapy: * At least 4 weeks since prior radiotherapy Surgery: * Not specified
References
Publications (0)
Data not yet available
No reference posted for this study.