CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 60 enrolled / 60 target
Drug / intervention
Tacrolimus +6 moredrug
Likely dose
10 mcg/kgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02782546
NCT02782546Phase 2ActiveUpdate Overdue (0.5/mo)Completion was 8mo ago

A Phase II Study of Cytokine Induced Memory-like NK Cell Adoptive Therapy After Haploidentical Donor Hematopoietic Cell Transplantation

Washington University School of Medicine·interventional·Posted May 25, 2016·Updated Jun 25, 2026

In Brief

A Phase 2 clinical trial evaluating Graft cell infusion, Tacrolimus, and 5 other interventions for Acute Myeloid Leukemia. Active but no longer recruiting, targeting 60 participants across 1 site.

Signals

Enrollment appears stalled

Detailed Summary

This is a standard phase 2 study powered to demonstrate improvement in the 100 day leukemia free survival to 30% from \<10% expected with the use of reduced intensity haplo-HCT in this extremely high-risk patient cohort (based on the institutional experience using non-myeloablative / reduced intensity conditioning in a similar patient cohort). A formal safety evaluation will be done after every 6th patient enrolled and the trial will be stopped if noted to have unusually higher engraftment failure (acute GVHD rates (\>60% any grades or \>30% grade III/IV or ≥ 50% severe cGVHD) or engraftment failure rates (≥15%).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2Active
201720182019202020212022202320242025202620272028
First PostedMay 25, 2016
Enrollment StartJan 30, 2017
Primary CompletionOct 27, 2025
Study CompletionFeb 13, 2028
TodayJul 2, 2026
Enrollment to primary: 8.7 yearsPosted 10.1 years ago

Arms & Interventions

Recipientexperimental

* Standard of care reduced conditioning regimen on Day -1 * Graft cell infusion on Day 0 * Post-transplant cyclophosphamide on Days +3 and +4 * GvHD prophylaxis with tacrolimus and mycophenolate mofetil (MMF) will start on Day +5. MMF will continue till Day +35 and tacrolimus till Day +180 in the absence of GvHD * G-CSF will start on Day +7 and will continue until neutrophil engraftment as per institutional guidelines * The cytokine-induced memory like natural killer (CIML NK) cells will be infused on Day +7 without a filter or pump, slowly by gravity over at least 15 minutes. * ALT-803 will start approximately 4 hours after the CIML NK cell infusion. ALT-803 will be administered subcutaneously at a dose of 10 mcg/kg subcutaneously beginning Day +7 (on the day of CIML NK cell infusion) and then every 21 days for a total of 4 doses

Procedure: Graft cell infusionDrug: TacrolimusDrug: Mycophenolate mofetilDrug: G-CSFProcedure: CIML NK cell infusionDrug: ALT-803
Donorexperimental

* Donors will receive subcutaneous G-CSF from Day -4 till Day 0 and undergo 20L apheresis per institutional guidelines. * Two consecutive days for collection are allowed in case of the target CD34+ cell dose being less than the target 4 x106/kg-bw from the first day of collection. * On Day +6 (one day before the planned CIML NK cell infusion), peripheral blood mononuclear cells will be collected by a single standard 20-L apheresis over 4-5 hours from the same haploidentical related donor that provided the HCT graft.

Procedure: Leukapheresis

Interventions

Graft cell infusionprocedure

-Day 0

Tacrolimusdrug

-GVHD prophylaxis

Mycophenolate mofetildrug

-GVHD prophylaxis

G-CSFdrug

-Continue until neutrophil engraftment as per institutional guidelines

CIML NK cell infusionprocedure

-Day +7

ALT-803drug

-Start approximately 4 hours after CIML NK cell infusion

Leukapheresisprocedure

-Day +6