Phase I/II Trial of Keratinocyte Growth Factor (rHuKGF) to Prevent Acute GVHD in 6/6 HLA=BMT Recipients
Trial Snapshot
- Phase
- Phase 1
- Status
- Completed
- Sponsor
- Enrollment
- 72
- Locations
- 2
Study Overview
Brief Summary
This is a study to determine the safety and efficacy of keratinocyte growth factor (KGF) to prevent acute graft-versus-host disease (GVHD) in patients undergoing allogeneic bone marrow (BM) or peripheral blood progenitor cell (PBPC) transplantation.
Detailed Description
GVHD remains the major complication of allogeneic BM transplantation and is initiated during the conditioning of the recipient for transplant when the host tissues are damaged. Research has demonstrated that the gastrointestinal (GI) tract is a critical organ in GVHD pathophysiology. Agents that protect the GI tract may provide prophylaxis against the cytokine cascade and can lead to a reduced incidence and severity of GVHD. KGF is a protein that stimulates the growth of epithelial cells including those of the GI tract. KGF can protect the GI tract, prevent GVHD, and preserve donor T-cell function.
Patients will receive standard GVHD prophylaxis in addition to the study drug. Overall GVHD will be graded weekly during the first 2 months after transplant, then every other week to Day 100. Response to therapy will be measured through the use of severity indices, physical exam, and laboratory serum values.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Primary Purpose
- Prevention
- Masking
- Double
Eligibility Criteria
- Ages
- 3 Years to 65 Years (Child, Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Diagnosis of a hematological malignancy, including myelodysplastic syndromes.
- •Eligible for cyclophosphamide and total body irradiation conditioning therapy or busulphan and cyclophosphamide conditioning therapy.
- •Must have a 6/6 human leukocyte antigens (HLA)-matched family member donor.
- •Women must be post-menopausal, sterile, or using effective contraception for 1 month before, during, and for 2 months after study.
- •Eastern Cooperative Oncology Group (ECOG) performance status 0-2.
Exclusion Criteria
- •T-cell depletion for GVHD prophylaxis.
- •Active hepatitis.
- •Pre-existent inflammatory bowel disease requiring active therapy.
- •Active uncontrolled infection.
- •Prior bone marrow or peripheral blood stem cell (PBSC) transplantation.
- •Documented hypersensitivity to rHuKGF.
- •Prior enrollment to a study of rHuKGF.
- •HIV-positive.
- •Pregnant or nursing.
- •Active chronic skin disease requiring therapy.