Clinical trial · Interventional
Chemotherapy Followed by Infusion of Partially HLA Matched Unrelated Donor Cells for Patients With AML Who Are Ineligible for Stem Cell Transplantation
NCT02189824CI-TRIAL-00019668SCRAMBLEunknownPhase 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)
A phase 1 study of infusion of partially HLA matched unrelated donor blood or marrow cells (microtransplantation) following consolidation chemotherapy in patients with AML that are not suitable for allogenic stem cell transplantation.
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 |
|---|---|---|---|
| Acute Myeloid Leukaemia | Acute Myeloid Leukemia | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Partially HLA-matched unrelated donor cells | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Infusion of partially matched unrelated donor cells
- interventionNames
- Biological: Partially HLA-matched unrelated donor cells
Primary outcomes (1)
- measure
- Incidence of acute graft versus host disease within 60 days of completion of final infusion of donor lymphocytes
- timeFrame
- 60 days
Secondary outcomes (3)
- measure
- Duration of post chemotherapy cytopenias
- timeFrame
- 60 days
- measure
- Remission rate
- timeFrame
- 12 months
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion Criteria: 1. Newly diagnosed AML not considered suitable for allogenic stem cell transplant on the basis of age or co-morbidities 2. Complete morphological remission following 1-2 cycles of induction chemotherapy consisting of an anthracycline/cytosine arabinoside combination 3. Availability of cryopreserved donor stem cells or bone marrow with appropriate HLA matching 4. Adequate hepatic and renal function 5. Estimated life expectancy of at least 6 months 6. Patient has given informed consent or in the event of a patient not able to give informed consent, consent has been given according to hospital procedures in force at the time of trial Exclusion Criteria: 1. Patient not in morphological remission following 2 cycles of induction chemotherapy 2. Use of fludarabine or other purine analogue during remission induction or use of any major immunosuppressive medication or any other immunomodulatory agent including thalidomide, lenalidomide, or azacitidine immediately prior to concurrent with administration of chemotherapy for AML or during or in the 3 months after administration of partially HLA matched 3rd party cells 3. Absence of a cryopreserved donor stem cell or bone marrow product with appropriate matching 4. Presence of significant hepatic, renal or other major organ dysfunction 5. Uncontrolled infection or bleeding prior to commencement of consolidation chemotherapy 6. Privately insured in or outpatient on the day the consent is signed and the days that cryopreserved partially HLA matched donor cells are infused
References
Publications (0)
Data not yet available
No reference posted for this study.