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NCT01746849Active, not recruitingPhase 2

Palifermin With Leuprolide Acetate for the Promotion of Immune Recovery Following Total Body Irradiation Based T-Cell Depleted Allogeneic Hematopoietic Stem Cell Transplantation

Phase II Study of Palifermin With Leuprolide Acetate or Degarelix For the Promotion of Immune Recovery Following Total Body Irradiation Based T-Cell Depleted Allogeneic Hematopoietic Stem Cell Transplantation

Source: ClinicalTrials.gov · Last updated 7 Jan 2026

Brief summary (registry, in English)

The purpose of this study is to help determine if palifermin and leuprolide acetate can help the immune system recover faster following a stem cell transplant. Blood stem cells are very young blood cells that grow in the body to become red or white blood cells or platelets. The transplant uses stem cells in the blood from another person. The donor can be a family member or a volunteer donor. This is called an allogeneic stem cell transplant. The investigators want to see if palifermin and leuprolide acetate can help the immune system recover faster after an allogenic transplant because experiments have shown they may be able to do this.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
82 (actual)
First submitted
7 Dec 2012
Start date
Dec 2012
Primary completion date
Dec 2026
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT01746849

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 82
  • From Dec 2012 to the primary completion date, Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who have undergone a prior allogeneic or autologous stem cell transplant within the previous six months.

Other illness

  • Active extramedullary disease
  • Active and uncontrolled infection at time of transplantation
  • HIV infection

Other

  • Pregnant or breast feeding
  • Patient is felt to not be a candidate for TBI by the BMT service
    • Donor Inclusion Criteria:
  • Donor must be willing and able to undergo PBSC collection.

Who the study is looking for

  • Treatment Portion:
  • AML in 1st remission - for patients whose AML does not have "good risk" cytogenetic features (i.e. t (8;21), t(15;17), inv 16 without c-kit mutations).
  • Acute leukemias of ambiguous lineage in ≥ 1st remission
  • Secondary AML in remission
  • AML in ≥ 2nd remission
  • ALL in 1st remission with clinical or molecular features indicating a high risk for relapse; or ALL ≥ 2nd remission
  • CML failing to respond to or not tolerating imatinib, dasatinib or nilotinib in first chronic phase of disease; CML in accelerated phase, second chronic phase, or in CR after accelerated phase or blast crisis.
  • Non-Hodgkins lymphoma with chemo responsive disease in any of the following categories:
    • intermediate or high grade lymphomas who have failed to achieve a first CR or have relapsed following a 1st remission who are not candidates for autologous transplants.
    • b.ii. any NHL in remission which is considered not curable with chemotherapy alone and not eligible/appropriate for autologous transplant.
  • Myelodysplastic syndrome (MDS): RA/RCMD with high risk cytogenetic features or transfusion dependence, RAEB-1 and RAEB-2
  • Chronic myelomonocytic leukemia: CMML-1 and CMML-2.
  • Patient's age is ≥18 or ≤60 years old
  • Patients must have a Karnofsky (adult) or Lansky (pediatric) Performance Status ≥ 70%
  • Patients must have adequate organ function measured by:
    • Cardiac: asymptomatic or if symptomatic then LVEF at rest must be \> 50% and must improve with exercise.
  • Pulmonary: asymptomatic or if symptomatic, DLCO \> 60% of predicted (corrected for hemoglobin)
  • Hepatic: \< 3xULN ALT and \< 1.5 total serum bilirubin, unless there is congenital benign hyperbilirubinemia
  • Renal: serum creatinine \< 1.2 mg/dL or if serum creatinine is outside the normal range, the CrCl \> 50 ml/min (measured or calculated/estimated)
  • Patients have a plan to receive a CD34-selected peripheral blood stem cell transplant with TBI-based conditioning.

Age in the registry: 18 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Memorial Sloan-Kettering Cancer Center
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.