GVHD
An Expanded Access Program of Ruxolitinib for the Treatment of Graft-Versus-Host Disease Following Allogeneic Hematopoietic Stem Cell Transplant
Incyte Study ID:
INCB 18424-MA-GD-301
CT.gov ID:
Eudra ID:
N/A
Sponsor:
Incyte Corporation
Collaborator:
N/A
Study Contact Information:
Clinical Study Purpose
To provide ruxolitinib through an expanded access program for the treatment of graft-versus-host disease (GVHD) in United States to patients who are ineligible or unable to participate in any actively enrolling Incyte-sponsored clinical studies for ruxolitinib in the treatment of GVHD.
Clinical Study Summary

MEDICAL CONDITION(S)

PRODUCT

COLLABORATORS
N/A

DATE
N/A - N/A

TYPE
Expanded Access

PHASE
N/A

SEX
Female & Male

AGE
12+ years

ACCEPTS HEALTHY VOLUNTEERS
Clinical Study Locations
Name
Avera Research Institute
Sioux Falls, South Dakota, US, 57105
Status
Completed
Name
Memorial Sloan Kettering Cancer Center
New York, New York, US, 10065
Status
Completed
Name
Greenville Health System Cancer Institute
Greenville, South Carolina, US, 29615
Status
Completed
Name
Cancer Center of Kansas
Wichita, Kansas, US, 67214
Status
Completed
Name
Hackensack University Medical Center
Hackensack, New Jersey, US, 07601
Status
Completed
Name
Oregon Health & Science University
Portland, Oregon, US, 97239
Status
Completed
Key Inclusion and Exclusion Criteria
Inclusion Criteria
- Male or female, 12 years of age or older.
- Have undergone an allo-HSCT from any donor source using bone marrow, peripheral blood stem cells, or cord blood for hematologic malignancies. Recipients of nonmyeloablative and myeloablative conditioning regimens are eligible.
Exclusion Criteria
- Eligible for an existing and actively enrolling Incyte sponsored clinical trial for ruxolitinib for the treatment of GVHD.
- Clinically suspected all grades of acute GVHD as per Minnesota-Center for International Blood and Marrow Transplant Research (MN-CIBMTR) criteria or clinical suspicion of acute GVHD by the treating physician.
Protocol Summary
Incyte Study ID:
INCB 18424-MA-GD-301
Primary Purpose:
N/A
Allocation:
N/A
Study Design:
N/A
Masking:
N/A
Interventions:
Drug
Enrollment:
Primary Outcome
Open
Secondary Outcome
Open