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
EU CT Number:
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 - Invalid Date
TYPE
Expanded Access
PHASE
N/A
SEX
Female & Male
AGE
12+ years
ACCEPTS HEALTHY VOLUNTEERS
N/A
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
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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.
Requirements information
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.
- • Clinically suspected all grades chronic GVHD according to NIH Consensus Criteria that is refractory or intolerant to corticosteroids, occurring after allo-HSCT with any conditioning regimen and any anti-GVHD prophylactic regimen. Clinical suspicion of steroid-refractory chronic GVHD by the treating physician is also sufficient.
- • Evidence of myeloid engraftment (eg, absolute neutrophil count ≥ 1.0 × 10^9/L for 3 consecutive days if ablative therapy was previously used). Use of growth factor supplementation is allowed.
- • Evidence of platelet engraftment (ie, platelets ≥ 20 × 10^9/L).
- • Eastern Cooperative Oncology Group (ECOG) performance status 0 to 3.
- • Be willing to avoid pregnancy or fathering children based on 1 of the following criteria:
- o Women of non-childbearing potential (ie, surgically sterile with a hysterectomy and/or bilateral oophorectomy OR ≥ 12 months of amenorrhea).
- o Woman of childbearing potential who has a negative serum pregnancy test at screening and who agrees to take appropriate precautions to avoid pregnancy (with at least 99% certainty) from screening through safety follow-up. Permitted methods that are at least 99% effective in preventing pregnancy should be communicated to the patient and their understanding confirmed.
- o Man who agrees to take appropriate precautions to avoid fathering children (with at least 99% certainty) from screening through safety follow-up. Permitted methods that are at least 99% effective in preventing pregnancy should be communicated to the patient and their understanding confirmed.
- • Able to provide written informed consent and/or assent from the patient, parent, or guardian.
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.
- • Patients or legal guardians unable to review and sign informed consent form.
- • Females who are pregnant or breastfeeding, and males and females who cannot comply with requirements to avoid fathering a child or becoming pregnant.
- • Patients with inadequate liver function (alanine aminotransferase above 4 × upper limit of normal (ULN) or direct bilirubin 4 × ULN and the laboratory abnormalities are considered to be due to underlying liver dysfunction) unless attributed to GVHD.
- • Patients with end stage renal function (creatinine clearance (CrCl) < 15 mL/min or glomerular filtration rate < 15 mL/min), regardless of whether hemodialysis is required.
- • Any underlying or current medical or psychiatric condition that, in the opinion of the treating physician, would place the patient at an unacceptable risk if he or she were to participate in the program.
- • Previous allergic reactions to Janus kinase (JAK) inhibitors or excipients.
- • Patients who are currently taking any anticancer therapy (eg, chemotherapy, radiation therapy, surgery, immunotherapy, biologic therapy, hormonal therapy, or tumor embolization).
- • Concomitant use of any JAK inhibitor.
- • Initiating therapy with any investigational medication.
- • Presence of an active uncontrolled infection. An active uncontrolled infection is defined as hemodynamic instability attributable to sepsis or new symptoms, worsening physical signs, or radiographic findings attributable to infection. Persisting fever without signs or symptoms will not be interpreted as an active uncontrolled infection.
- • Known HIV infection.
- • Active hepatitis B virus (HBV) or hepatitis C virus infection that requires treatment or at risk for HBV reactivation. At risk for HBV reactivation is defined as hepatitis B surface antigen positive or anti-hepatitis B core antibody positive. Previous test results obtained as part of standard of care before allo-HSCT that confirm a patient is immune and not at risk for reactivation (ie, hepatitis B surface antigen negative, surface antibody positive) may be used for purposes of eligibility.
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:
Enrollment:
N/A
Primary Outcome
Open
Not Available
Secondary Outcome
Open
Not Available