Status:
COMPLETED
RGI-2001 for the Prevention of Acute Graft-vs-Host Disease in Subjects Following Allogeneic Hematopoietic Stem Cell Transplantation
Lead Sponsor:
Regimmune Corporation
Conditions:
Graft Vs Host Disease
Graft-versus-host-disease
Eligibility:
All Genders
18-64 years
Phase:
PHASE2
Brief Summary
This Phase II open label study will evaluate the safety and efficacy of repeat doses of RGI-2001 in combination with standard of care treatment for the prevention of acute graft-vs-host-disease (aGvHD...
Detailed Description
This is an open-label, multi-center, single-arm study to evaluate six weekly doses of RGI-2001 in combination with standard of care treatment for the prevention of aGvHD in subjects following alloHSCT...
Eligibility Criteria
Inclusion
- Ages ≥ 18 and ≤ 65 years of age
- Has a hematologic malignancy which includes Acute myelogenous leukemia (AML), T or B cell acute lymphoblastic leukemia (ALL) Myelodysplastic syndrome (MDS), chronic myelomonocytic leukemia (CMML), myeloproliferative disorder (MPD) including myeloid metaplasia and CML
- Must have adequate organ function
- Transplant Donor: Matched related donor or Unrelated donor
- Is a candidate for anti-graft-vs-host-disease (GvHD) prophylaxis that includes a calcineurin inhibitor
- Ability to understand and willingness to sign a written informed consent form
- If female of childbearing potential, must have had a negative serum pregnancy test prior to enrollment and must have agreed to use a double barrier method of contraception for 30 days after RGI-2001 administration
- If male, must be sterile or willing to use an approved method of contraception from the time of informed consent to 90 days after last dose of RGI-2001 administration
Exclusion
- Has had any other prior organ transplantation
- Planned procedure to deplete regulatory T cells from donor transplant materials
- Planned reduced intensity conditioning
- Has had prior treatment with anti-CD3, other T cell depleting antibodies, or anti-thymocyte globulin within 12 months prior to alloHSCT procedure
- Has progressive underlying malignant disease including post-transplant lymphoproliferative disease
- Has evidence of active central nervous system (CNS) disease including known brain or leptomeningeal disease (CT or MRI scan of the brain required only in case of clinical suspicion of CNS involvement)
- Is female and pregnant or lactating
- Has a documented history of uncontrolled autoimmune disease or on active treatment
- History of myocardial infarction, unstable angina, or acute coronary syndrome within 6 months prior to receiving study drug
Key Trial Info
Start Date :
November 25 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 3 2023
Estimated Enrollment :
49 Patients enrolled
Trial Details
Trial ID
NCT04014790
Start Date
November 25 2019
End Date
April 3 2023
Last Update
May 28 2024
Active Locations (7)
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1
UCLA Medical Center
Los Angeles, California, United States, 90095
2
University of Miami, Sylvester Comprehensive Cancer Center
Miami, Florida, United States, 33136
3
University of Maryland Greenebaum Comprehensive Cancer Center
Baltimore, Maryland, United States, 21201
4
Massachusetts General Hospital
Boston, Massachusetts, United States, 02114