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Graft vs Host Disease clinical trials

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NCT ID: NCT02945176 Completed - Clinical trials for Graft vs Host Disease

Safety and Performance Study of the ARGOS-IO System in Patients Undergoing Boston Keratoprosthesis Implantation

Start date: March 2015
Phase: N/A
Study type: Interventional

The ARGOS-IO pressure sensor is intended to be implanted in the human eye in combination with Boston Keratoprosthesis (BKPro) surgery and to remain in place indefinitely. It is intended to be used together with the hand-held Mesograph reading device to telemetrically measure the intraocular pressure (IOP) of patients with a BKPro. The purpose of this study is to evaluate the safety and performance of the ARGOS-IO system in patients undergoing concomitant implantation of a BKPro and an ARGOS-IO sensor over the 12 month period beginning at implantation.

NCT ID: NCT02942173 Completed - Lymphoma Clinical Trials

CD45RA Depleted T-cell Infusion for Prevention of Infections After TCRab/CD19-depleted Allo-HSCT

Start date: October 2016
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this prospective randomized study is to determine whether infusions of T-memory cells prevent infections in children with leukemia after allogeneic alpha, beta T-cell receptor (TcRab)/CD19-depleted hematopoietic stem cell transplantation (HSCT).

NCT ID: NCT02923375 Completed - Clinical trials for Graft vs Host Disease

A Study of CYP-001 for the Treatment of Steroid-Resistant Acute Graft Versus Host Disease

Start date: March 1, 2017
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess the safety, tolerability and efficacy of two infusions of CYP-001 in adults with steroid-resistant GvHD.

NCT ID: NCT02918188 Recruiting - Clinical trials for Chronic Graft-versus-host Disease

Therapeutic Effects of Hydrogen on Steroid-refractory/or Steroid-dependent cGVHD

Start date: January 2016
Phase: Phase 2
Study type: Interventional

This study suggested that hydrogen has a potential as an effective and safe therapeutic agent on cGVHD.

NCT ID: NCT02917148 Withdrawn - Acute GVH Disease Clinical Trials

MicroRNAs as Diagnostic and Predictive Biomarkers for Acute Graft Versus Host Disease

Start date: September 2016
Phase: N/A
Study type: Observational

The goal of this research proposal is to identify a miRNA expression profile as a biomarker to diagnose and predict acute graft versus host disease (aGVHD) in patients who undergo allogeneic transplantation. This biomarker, once identified, will need validation in larger cohorts.

NCT ID: NCT02913261 Completed - Clinical trials for Corticosteroid Refractory Acute Graft vs Host Disease

Safety and Efficacy of Ruxolitinib Versus Best Available Therapy in Patients With Corticosteroid-refractory Acute Graft vs. Host Disease After Allogeneic Stem Cell Transplantation

REACH2
Start date: March 10, 2017
Phase: Phase 3
Study type: Interventional

Assess the efficacy and safety of ruxolitinib compared to Best Available Therapy (BAT) in patients with corticosteroid-refractory acute graft vs. host disease (aGvHD) after allogeneic stem cell transplantation.

NCT ID: NCT02891603 Completed - Clinical trials for Graft Vs Host Disease

A Phase I/II GVHD Prevention Trial Combining Pacritinib With Sirolimus-Based Immune Suppression

Start date: June 8, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to examine a new approach to preventing a serious problem after transplant called graft vs. host disease (abbreviated as GVHD). This is a 3 arm sequential phase I/II, study of Pacritinib with Sirolimus and Tacrolimus (PAC/SIR/TAC) for the prevention of acute GVHD after matched related and unrelated allogeneic hematopoietic cell transplantation (alloHCT).

NCT ID: NCT02891395 Completed - Clinical trials for Graft Versus Host Disease

Efficacy and Safety of Nilotinib in Patients With a Chronic Disease of the Graft Against the Host

DoubleITK
Start date: December 24, 2012
Phase: Phase 2
Study type: Interventional

Open label non-randomized multicenter phase 2 trial with direct individual benefice

NCT ID: NCT02877082 Terminated - Clinical trials for Chronic Lymphocytic Leukemia

Tacrolimus, Bortezomib, & Thymoglobulin in Preventing Low Toxicity GVHD in Donor Blood Stem Cell Transplant Patients

Start date: September 2016
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well tacrolimus, bortezomib, and anti-thymocyte globulin (thymoglobulin) work in preventing low toxicity graft versus host disease (GVHD) in patients with blood cancer who are undergoing donor stem cell transplant. Tacrolimus and anti-thymocyte globulin may reduce the risk of the recipient's body rejecting the transplant by suppressing the recipient's immune system. Giving bortezomib after the transplant may help prevent GVHD by stopping the donor's cells from attacking the recipient. Giving tacrolimus, bortezomib, and anti-thymocyte globulin may be a better way to prevent low toxicity GVHD in patients with blood cancer undergoing donor stem cell transplant.

NCT ID: NCT02876679 Completed - Clinical trials for Graft vs Host Disease

Cyclophosphamide Versus Anti-thymocyte Globulin for GVHD Prophylaxis After RIC Allo-SCT

ATG-CyGVHD
Start date: April 6, 2017
Phase: Phase 2
Study type: Interventional

The study is designed as a two arm randomized Phase II, multicenter trial comparing cyclophosphamide to anti-thymocyte globulin for Graft-versus-Host Disease (GVHD) prophylaxis in patients with hematologic malignancies undergoing reduced intensity conditioning hematopoietic stem cell transplantation.