Motixafortide for MRD Sensitization in AML
Part of paid clinical trials in St Louis, Missouri.
- Sponsor
- Washington University School of Medicine
- Study ID
- NCT07392970
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Acute Myeloid Leukemia
- Measurable Residual Disease
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Motixafortide — DRUGMotixafortide is a CXCR4 inhibitor for the mobilization of hematopoietic stem progenitor cells (HSPCs) in patients undergoing autologous stem cell transplantation. It is provided as a single subcutaneous injection.
Study Details
This is a pilot phase I study evaluating the effect of motixafortide on determination of measurable residual disease (MRD) level in patients with acute myeloid leukemia (AML) who have completed induction treatment. Consenting and eligible patients will undergo standard of care (SOC) bone marrow and peripheral blood assessments with SOC MRD assays, followed by a single injection of motixafortide. Ten to 14 hours after injection, the patient will undergo peripheral blood collection for the same applicable MRD tests
Key Dates
- First listed
- Feb 6, 2026
- Start date
- Jul 23, 2026
- Status verified
- Jul 2026
- Primary completion
- Aug 2, 2028
- Completion
- Feb 2, 2030
Study Design
- Enrollment
- 10 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- DIAGNOSTIC
Arms
- Experimental: Motixafortide InjectionConsenting and eligible patients will bone marrow and peripheral blood testing assessments along with measurable residual disease (MRD) assays. Following completion of assessments, patients will receive a single injection of Motixafortide. The following day, 10-14 hours after the injection, patients will repeat the peripheral blood testing for MRD tests. Investigators will follow up with patients every 4 months for 18 months after study treatment.
Primary Outcome Measure
Efficacy of motixafortide on measurable residual disease (MRD) levels [ Time Frame: Day 1 before motixafortide and Day 2 (estimated total time is 2 days) ]
Central Contacts
- Samuel Urrutia, MD314-273-6734
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Washington University School of Medicine | St Louis | Missouri | 63110 | Samuel Urrutia, MD (PRINCIPAL_INVESTIGATOR) John F DiPersio, MD, PhD (SUB_INVESTIGATOR) Feng Gao, MD, PhD, MPH (SUB_INVESTIGATOR) Ningying Wu, MD, PhD (SUB_INVESTIGATOR) |
Find similar trials in St Louis, MO
By condition
By specialty
By research site
Related Studies
- A Study of Revumenib in R/R Leukemias Including Those With an MLL/KMT2A Gene Rearrangement or NPM1 MutationPHASE1/PHASE2 · Recruiting · Syndax Pharmaceuticals · Aurora, Colorado
- A Safety Study of SEA-CD70 in Patients With Myeloid MalignanciesPHASE1 · Recruiting · Seagen, a wholly owned subsidiary of Pfizer · Duarte, California
- A Study to Compare Standard Chemotherapy to Therapy With CPX-351 and/or Gilteritinib for Patients With Newly Diagnosed AML With or Without FLT3 MutationsPHASE3 · Recruiting · Children's Oncology Group · Birmingham, Alabama
- The Pediatric Acute Leukemia (PedAL) Screening Trial - A Study to Test Bone Marrow and Blood in Children With Leukemia That Has Come Back After Treatment or Is Difficult to Treat - A Leukemia & Lymphoma Society and Children's Oncology Group StudyPHASE1/PHASE2 · Recruiting · PedAL BCU, LLC · Birmingham, Alabama