Graft Versus Host Disease (GVHD)

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Review clinical trials related to Graft Versus Host Disease (GVHD). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Study of Tacrolimus/Methotrexate/Ruxolitinib Versus Post-Transplant Cyclophosphamide/Tacrolimus/Mycophenolate Mofetil in Non-Myeloablative/Reduced Intensity Conditioning Allogeneic Peripheral Blood Stem Cell Transplantation (BMT CTN 2203)

The purpose of this study is to assess Tacrolimus/Methotrexate/Ruxolitinib versus Post-Transplant Cyclophosphamide/Tacrolimus/Mycophenolate Mofetil in Non-Myeloablative/Reduced Intensity Conditioning Allogeneic Peripheral Blood Stem Cell Transplantation

Participants needed: 572
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Incyte CorporationUpdated: May 20, 2026Locations: 30
Eligibility criteria

Age 18.0 years or older at the time of enrollment. [+16]

Prior allogeneic transplant. [+20]

Status: Recruiting

Allogeneic HSCT With Low-Dose Post-Transplant Cyclophosphamide for GVHD Prevention

This Phase 2, single-arm, open-label study aims to evaluate the safety and efficacy of low-dose (25 mg/kg) post-transplant cyclophosphamide (PTCy) for prophylaxis of Graft-versus-Host Disease (GVHD) in patients undergoing allogeneic stem cell transplantation following reduced-intensity or non-myeloablative conditioning. The study will focus on matched sibling, matched unrelated, and haploidentical peripheral blood stem cell donors. The primary endpoint is 1-year GVHD-Free Relapse-Free Survival (GRFS). The study seeks to determine if low-dose PTCy offers similar outcomes as higher doses, with potentially reduced toxicity.

Participants needed: 41
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Milton S. Hershey Medical CenterUpdated: Apr 3, 2026Locations: 1
Eligibility criteria

Age 18 or older at the time of study enrollment. [+12]

Prior allogeneic stem cell transplant. [+10]

Status: Not yet recruiting

Vitamin C With Steroids for Gastrointestinal GVHD

After a transplant from another donor, one risk is graft versus host disease (GVHD) that happens because of differences between the donated cells (graft) and the patient's body cells (host). The new cells from the donor might see the body's cells as different and attack them. GVHD can be very serious and cause death. The standard first treatment for GVHD is corticosteroids but not all patients respond and in cases where they don't, they need to go onto other treatments that may or may not be effective. In addition, when GHVD involves the gut it can damage the cells of the gastrointestinal track causing long term problems such as abdominal pain and bowel disturbance. In laboratory studies giving a vitamin C has been able to protect the gastrointestinal cells and help them recover. In this trial the investigators would like to see if vitamin C can do the same thing when given with steroids in patients with GVHD. The standard first treatment for acute GVHD is corticosteroids but not all patients respond and in cases where they don't, they need to go onto other treatments that may or may not be effective. In addition, when GHVD involves the gut it can damage the cells of the gastrointestinal track causing long term problems such as abdominal pain and bowel disturbance. In the laboratory vitamin C has been able to protect gut stem cells and help them recover and the investigators would like to learn if this happens in people too. Vitamin C is a readily available supplement. Vitamin C has NOT been approved by the FDA for the treatment of acute GVHD.

Participants needed: 35
Trial details
Phase: Early Phase 1Age: 5+Biological sex: AllType: InterventionalSponsor: Baylor College of MedicineUpdated: Mar 4, 2026
Eligibility criteria

Patients 5 years of age or older at time of enrollment. [+4]

Relapsed, progressing or persistent malignancy or evidence of minimal residual d... [+13]

Status: Recruiting

Optimizing GVHD Prophylaxis After Allogeneic Hematopoietic Cell Transplantation

This study will compare post-transplant health-related quality of life following the use of standard versus attenuated dose of post-transplant cyclophosphamide in addition to two-drug graft-versus-host disease (GVHD) prophylaxis among recipients of allogeneic hematopoietic stem cell transplant.

Participants needed: 126
Trial details
Phase: Phase 2Age: 60+Biological sex: AllType: InterventionalSponsor: University of NebraskaUpdated: Dec 15, 2025Locations: 1
Eligibility criteria

Adults aged 60 years or older [+3]

Previous history of one or more prior allogeneic stem cell transplants (i.e., se... [+7]

Status: Recruiting

Dapagliflozin in Allo-HCT for aGVHD

The goal of this clinical trial is to learn if Dapagliflozin could prevent acute graft-versus-host disease (aGVHD) in patients undergoing allogeneic hematopoietic cell transplantation (allo-HCT) with haploidentical or unrelated donor and to assess its safety. The main questions it aims to answer are: Dose Dapagliflozin lower the cumulative incidence of aGVHD? What medical problems do participants undergoing allo-HCT from haploidentical or unrelated donor have when taking Dapagliflozin? Researchers will document the occurrence of graft-versus-host disease, hematopoietic reconstitution, survival rates and adverse effects. Participants will take Dapagliflozin every day in -1 to 14 days.

Participants needed: 72
Trial details
Phase: Phase 2Age: 18-65Biological sex: AllType: InterventionalSponsor: The First Affiliated Hospital of Soochow UniversityUpdated: Jun 5, 2025Locations: 1
Eligibility criteria

Age 18 to 65 years old. [+5]

With other malignancies. [+8]