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Immunomodulator

Cyclophosphamide + Abatacept for Graft-versus-Host Disease

Phase 2
Waitlist Available
Led By Divya Koura, MD
Research Sponsored by Dimitrios Tzachanis, MD PhD
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
High risk hematologic malignancy justifying the need for an allogeneic hematopoetic stem cell transplantation: AML, ALL, CML in accelerated or blast phase, MDS/MPN, NHL, Hodgkin lymphoma, and multiple myeloma
Normal cardiac function (EF > 50%)
Must not have
Patients with hematologic malignancies for which transplant is not the only curative option, such as AML with good or intermediate cytogenetics or molecular markers in CR1 or CML in chronic phase
Inability to identify an 10/10 HLA-Matched Donor (related or unrelated) or a haploidentical donor
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, an average of 1 year
Awards & highlights
No Placebo-Only Group

Summary

This trial will compare two different treatments for GVHD.

Who is the study for?
This trial is for people with high-risk blood cancers needing a stem cell transplant and who have a perfectly matched or half-matched donor. They should not be pregnant, breastfeeding, or on other experimental drugs recently. People with active cancer relapse, short life expectancy, certain leukemia types in early stages, or uncontrolled infections and heart problems can't join.
What is being tested?
The study compares the effectiveness of Cyclophosphamide and Abatacept combination to standard treatments in preventing severe chronic graft-versus-host disease after stem cell transplantation. This condition happens when transplanted cells attack the patient's own body cells.
What are the potential side effects?
Possible side effects include immune system reactions like inflammation, infection risks due to weakened defenses, liver issues from medication toxicity, nausea from chemotherapy drugs like Methotrexate and Cyclophosphamide, as well as potential heart complications.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I have a high-risk blood cancer needing a stem cell transplant.
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My heart functions normally.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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My blood cancer can be treated with options other than a transplant.
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I cannot find a perfectly matched or half-matched donor for a transplant.
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My cancer has come back after treatment.
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I do not have any uncontrolled infections or heart problems.
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My leukemia is in its first chronic phase.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion, an average of 1 year for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Occurrence of Moderate and Severe Chronic GVHD at One Year Post Transplant
Secondary study objectives
GVHD- and Relapse- Free Survival by One Year Post Transplant

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Cyclophosphamide and abataceptExperimental Treatment2 Interventions
The GVHD prophylaxis regimen on the experimental arm will consist of high dose Cyclophosphamide on Days +3 and +4 followed by abatacept for 6 months. Abatacept at a dose of 10mg/kg will be administered on days +5, +14 and +28, +56, +84, +112, +140, +168
Group II: methotrexate and tacrolimusActive Control2 Interventions
The GVHD prophylaxis regimen on the standard of care arm will consist of methotrexate on Days +1,+3, +6 and +11 and tacrolimus
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Cyclophosphamide
2010
Completed Phase 4
~2310
abatacept
2006
Completed Phase 4
~1180

Find a Location

Who is running the clinical trial?

Dimitrios Tzachanis, MD PhDLead Sponsor
Bristol-Myers SquibbIndustry Sponsor
2,681 Previous Clinical Trials
4,124,941 Total Patients Enrolled
Divya Koura, MDPrincipal InvestigatorUniversity of California, San Diego

Media Library

Abatacept (Immunomodulator) Clinical Trial Eligibility Overview. Trial Name: NCT03680092 — Phase 2
Cancer Research Study Groups: Cyclophosphamide and abatacept, methotrexate and tacrolimus
Cancer Clinical Trial 2023: Abatacept Highlights & Side Effects. Trial Name: NCT03680092 — Phase 2
Abatacept (Immunomodulator) 2023 Treatment Timeline for Medical Study. Trial Name: NCT03680092 — Phase 2
~7 spots leftby Nov 2025