Recruiting
Phase 1

Emapalumab with Cyclophosphamide, Tacrolimus, Mycophenolate Mofetil

Sponsor:

City of Hope Medical Center

Code:

NCT06996119

Conditions

Acute Myeloid Leukemia

Graft Versus Host Disease

Myelodysplastic Syndrome

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

Biospecimen Collection

Busulfan

Computed Tomography

Cyclophosphamide

Echocardiography Test

Study Details

Brief summary:

This phase I trial tests the safety, side effects and effectiveness of emapalumab with post-transplant cyclophosphamide, tacrolimus, and mycophenolate mofetil in preventing graft-versus-host disease (GVHD) in patients with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) after reduced-intensity donor (allogeneic) hematopoietic cell transplant (HCT). Giving chemotherapy, such as fludarabine, melphalan, or busulfan, before a donor \[peripheral blood stem cell\] transplant helps kill cancer cells in the body and helps make room in the patient's bone marrow for new blood-forming cells (stem cells) to grow. When healthy stem cells for a donor are infused into a patient (allogeneic HCT), they may help the patient's bone marrow make more healthy cells and platelets. Allogeneic HCT is an established treatment, however, GVHD continues to be a major problem of allogeneic HCT that can complicate therapy. GVHD is a disease caused when cells from a donated stem cell graft attack the normal tissue of the transplant patient. Emapalumab binds to an immune system protein called interferon gamma. This may help lower the body's immune response and reduce inflammation. Cyclophosphamide is in a class of medications called alkylating agents. It works by damaging the cell's deoxyribonucleic acid and may kill cancer cells. It may also lower the body's immune response. Tacrolimus is a drug used to help reduce the risk of rejection by the body of organ and bone marrow transplants. Mycophenolate mofetil is a drug used to prevent GVHD after organ transplants. It is also being studied in the prevention of GVHD after stem cell transplants for cancer, and in the treatment of some autoimmune disorders. Mycophenolate mofetil is a type of immunosuppressive agent. Giving emapalumab with post-transplant cyclophosphamide, tacrolimus and mycophenolate mofetil may be safe, tolerable and/or effective in preventing GVHD in patients with AML or MDS after a reduced-intensity allogeneic HCT.

Conditions

Acute Myeloid Leukemia

Graft Versus Host Disease

Myelodysplastic Syndrome

Study ID

NCT06996119

Start date

Jun 12, 2026

Status verified date

May, 2026

Completion date

May 25, 2027

Anticipated

Primary completion date

May 25, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Documented informed consent of the participant and/or legally authorized representative

  • Assent, when appropriate, will be obtained per institutional guidelines
  • Age: ≥ 18 years and ≤ 75 years

  • Note: Patients > 70 years of age must have Karnofsky performance status ≥ 80% and HCT-comorbidity index (CI) ≤ 2
  • Karnofsky performance status ≥ 70%
  • Patients with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) in complete remission with bone marrow (BM) blast of < 5%. AML must be negative for minimal residual disease (MRD-)
  • Planned to undergo reduced-intensity conditioning (RIC) with either fludarabine/melphalan (Flu/Mel) or busulfan/fludarabine (Bu/Flu) regimens prior to an allogeneic HCT using a mobilized peripheral blood stem cell (PBMC) graft from an 8/8 match related/unrelated donor (A, B, C, DR by high resolution typing)
  • Total bilirubin ≤ 1.5 x upper limit of normal (ULN) (unless has Gilbert's disease)
  • Aspartate aminotransferase (AST) ≤ 3.0 x ULN
  • Alanine aminotransferase (ALT) ≤ 3.0 x ULN
  • Creatinine clearance of ≥ 60 mL/min per 24-hour urine test or the Cockcroft-Gault formula
  • Left ventricular ejection fraction (LVEF) ≥ 50%

  • Note: To be performed within 30 days prior to day 1 of protocol therapy
  • Bazett's correction formula (QTcB) ≤ 480 ms
  • If able to perform pulmonary function tests: forced expiratory volume in 1 second (FEV1), forced vital capacity (FVC) and diffusion capacity of the lung for carbon monoxide (DLCO) (diffusion capacity) ≥ 50% of predicted (corrected for hemoglobin).
  • If unable to perform pulmonary function tests: Oxygen (O2) saturation > 92% on room air
  • Seronegative for HIV antigen (Ag)/antibody (Ab) combo, hepatitis C virus (HCV), active hepatitis B virus (HBV) (surface antigen negative) OR

  • If seropositive for HIV, HCV or HBV, nucleic acid quantitation must be performed. Viral load must be undetectable
  • Meets other institutional and federal requirements for infectious disease titer requirements

  • Note Infectious disease testing to be performed within 28 days prior to day 1 of protocol therapy
  • QuantiFERON-TB Gold+

  • Administer tuberculosis prophylaxis to patients at risk for tuberculosis, or known to have a positive purified protein derivative (PPD) test result, or positive interferon gamma (IFNγ) release assay
  • Women of childbearing potential (WOCBP): negative urine or serum pregnancy test

  • If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required
  • Agreement by females and males of childbearing potential to use an effective method of birth control or abstain from heterosexual activity for the course of the study through at least 180 days post-HCT

  • Childbearing potential defined as not being surgically sterilized (men and women) or have not been free from menses for > 1 year (women only)

Exclusion Criteria:

  • Prior allogeneic HCT
  • Other cancer therapies (chemotherapy, radiation, biologics) are not allowed within two weeks of starting HCT conditioning; however targeted agents for underlying hematologic malignancies may be continued up to one day before conditioning, including, but not limited to:

  • FLT3 inhibitors
  • IDH1/2 inhibitors
  • Menin inhibitors
  • ABL-BCR inhibitors
  • BCL-2 inhibitors
  • Hydroxyurea
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to study agent
  • Psychological issues, no appropriate caregivers identified, or non-compliant to medication
  • Clinically significant uncontrolled illness
  • Active uncontrolled infections (bacterial, viral, fungal). Infections are considered controlled if appropriate therapy has been initiated and, at the time of screening, no signs of infection are present
  • Other active malignancy
  • Females only: Pregnant or breastfeeding
  • Any other condition that would, in the investigator's judgment, contraindicate the patient's participation in the clinical study due to safety concerns with clinical study procedures
  • Prospective participants who, in the opinion of the investigator, may not be able to comply with all study procedures (including compliance issues related to feasibility/logistics)

Study Design

Enrollment

15 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Prevention (emapalumab, cyclophosphamide)

Patients receive fludarabine IV on days -7 to -3 and melphalan IV over 1 hour on day -2 or busulfan IV on days -7 and -6 and fludarabine IV on days -7 to -2. Patients receive HCT infusion on day 0 per institutional standards of practice. Patients also receive emapalumab IV over 1 hour on days -8. -1, -7, 14 and 21, cyclophosphamide IV on days 3 and 4, tacrolimus IV or PO on days 5-95, mycophenolate mofetil IV or PO on days 5-35. Additionally, patients undergo chest CT and ECHO or MUGA at baseline and blood sample collection throughout the study.

Interventions

Biospecimen Collection

Undergo blood sample collection

Busulfan

Given IV

Computed Tomography

Undergo chest CT

Cyclophosphamide

Given IV

Echocardiography Test

Undergo ECHO

Emapalumab

Given IV

Fludarabine

Given IV

Hematopoietic Cell Transplantation

Given infusion

Melphalan

Given IV

Multigated Acquisition Scan

Undergo MUGA

Mycophenolate Mofetil

Given IV or PO

Questionnaire Administration

Ancillary studies

Tacrolimus

Given IV or PO

Primary outcome measure

  • Incidence of grade 3 or higher adverse events (AEs) [ Time Frame: From starting the first emapalumab dose to the first observation of a primary safety endpoint (PSE) event or day 28 post-hematopoietic cell transplantation (HCT), whichever comes first ]
  • Incidence of severe infusion reaction [ Time Frame: From starting the first emapalumab dose to the first observation of a PSE event or day 28 post-HCT, whichever comes first ]
  • Incidence of primary graft failure [ Time Frame: From starting the first emapalumab dose to the first observation of a PSE event or day 28 post-HCT, whichever comes first ]
  • Non-relapse mortality (NRM) [ Time Frame: From starting the first emapalumab dose to the first observation of a PSE event or day 28 post-HCT, whichever comes first ]

Central Contacts and Locations

Locations

City of Hope Medical Center

Recruiting

Duarte, California, United States, 91010

Contacts

Amandeep Salhotra

626-218-2405asalhotra@coh.org

Principal Investigator:

Amandeep Salhotra

More Information

Sponsor

City of Hope Medical Center

Last update posted

Jul 1, 2026

Last verified

May, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by City of Hope Medical Center on 2026-07-01.