Status:
ENROLLING_BY_INVITATION
Sequential Cadaveric Lung and Bone Marrow Transplant for Immune Deficiency Diseases
Lead Sponsor:
Paul Szabolcs
Conditions:
Severe Combined Immunodeficiency (SCID)
Immunodeficiency With Predominant T-cell Defect, Unspecified
Eligibility:
All Genders
5-45 years
Phase:
PHASE1
PHASE2
Brief Summary
The purpose of this study is to determine whether bilateral orthotopic lung transplantation (BOLT) followed by cadaveric partially-matched hematopoietic stem cell transplantation (HSCT) is safe and ef...
Detailed Description
This is an original IND for an investigator initiated phase I/II study. The primary purpose of the study is to evaluate the safety and efficacy of performing bilateral orthotopic lung transplantation ...
Eligibility Criteria
Inclusion
- Inclusion Criteria
- Subject and/or parent guardian must be able to understand and provide informed consent.
- Male or female, 5 through 45 years old, inclusive, at the time of informed consent.
- Patients must have evidence of an underlying primary immunodeficiency for which BMT is clinically indicated.
- Examples of such diseases include, but are not limited to:
- Severe Combined Immunodeficiency
- Combined immunodeficiency with defects in T-cell-mediated immunity, including Omenn syndrome and DiGeorge Syndrome
- Severe Chronic Neutropenia
- Chronic Granulomatous Disease
- Hyper IgE Syndrome or Job Syndrome
- CD40 or CD40L deficiency
- Wiskott-Aldrich Syndrome
- Mendelian Susceptibility to Mycobacterial Disease \[6\]
- GATA2 Associated Immunodeficiency NOTE: A genetic diagnosis is recommended, but not required.
- Patients must have evidence of end-stage lung disease and be candidates for bilateral orthotopic lung transplant as determined by the lung transplant team.
- GFR ≥ 50 mL/min/1.73 m2.
- AST, ALT ≤ 4x upper limit of normal, total bilirubin ≤ 2.5 mg/dL, normal INR.
- Cardiac ejection fraction ≥ 40% or shortening fraction ≥26%.
- Negative pregnancy test for females \>10 years old or who have reached menarche, unless surgically sterilized.
- All females of childbearing potential and sexually active males must agree to use a FDA approved method of birth control for up to 24 months after BMT or for as long as they are taking any medication that may harm a pregnancy, an unborn child or may cause birth defect.
- Subject and/or parent guardian will also be counseled regarding the potential risks of infertility following BMT and advised to discuss sperm banking or oocyte harvesting.
- Exclusion Criteria
- Individuals who meet any of these criteria are not eligible for this study:
- Inability or unwillingness of a participant to give written informed consent or comply with study protocol.
- Patients who have underlying malignant conditions.
- Patients who have non-malignant conditions not requiring hematopoietic stem cell transplantation.
- HIV positive by serology or PCR, HTLV positive by serology.
- Females who are pregnant or who are lactating.
- Allergy to DMSO or any other ingredient used in the manufacturing of the stem cell product.
- Uncontrolled pulmonary infection, as determined by radiographic findings and/or significant clinical deterioration. NOTE: Pulmonary colonization with multiple organisms is common, and will not be considered an exclusion criterion.
- Uncontrolled systemic infection, as determined by the appropriate confirmatory testing e.g. blood cultures, PCR testing, etc.
- Recent recipient of any licensed or investigational live attenuated vaccine(s) within 4 weeks of transplant.
- Past or current medical problems or findings from physical examination or laboratory testing that are not listed above, which, in the opinion of the investigator, may pose additional risks from participation in the study, may interfere with the participant's ability to comply with study requirements or that may impact the quality or interpretation of the data obtained from the study.
- Eligibility Criteria to proceed to Bone Marrow Transplant
- GFR ≥ 50 mL/min/1.73 m2.
- AST, ALT ≤ 4x upper limit of normal, total bilirubin ≤ 2.5 mg/dL.
- Cardiac ejection fraction ≥ 40% or shortening fraction of at least 26%.
- HIV negative by serology and PCR.
- HTLV serology negative.
- FVC and FEV1 ≥40% predicted for age and SpO2 of \>90% at rest on room air AND with clearance by the lung transplant team.
- Absence of uncontrolled infection as determined by positive blood cultures and radiographic progression of previous sites in particular pulmonary densities during the past 2 weeks prior to chemotherapy.
- Absence of clinically significant Acute Cellular Rejection (A2-A4 and/or B2R rejection).
Exclusion
Key Trial Info
Start Date :
June 20 2013
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
November 1 2027
Estimated Enrollment :
16 Patients enrolled
Trial Details
Trial ID
NCT01852370
Start Date
June 20 2013
End Date
November 1 2027
Last Update
December 15 2025
Active Locations (1)
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1
Children's Hospital of Pittsburgh of UPMC
Pittsburgh, Pennsylvania, United States, 15224