NCT03500731RecruitingPhase 1/2
Lung and Bone Marrow Transplantation for Lung and Bone Marrow Failure
Lung Transplant in Tandem With Bone Marrow Transplant for Combined Lung and Bone Marrow Failure
Source: ClinicalTrials.gov · Last updated 13 Jan 2026
Brief summary (registry, in English)
The purpose of this study is to determine whether a lung transplantation prior to bone marrow transplantation (BMT) would allow for restoration of pulmonary function prior to BMT, allowing to proceed to BMT, to restore hematologic function.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 1/2
- Study type
- Interventional
- Enrollment
- 8 (estimated)
- First submitted
- 30 Mar 2018
- Start date
- 19 Apr 2018
- Primary completion date
- Dec 2027
- Lead sponsor
- Paul Szabolcs
- Diseases
- Idiopathic pulmonary fibrosis, COPD
- NCT number
- NCT03500731
What you commit to
- Study type: Interventional · Phase 1/2
- Planned participants: 8
- From 19 Apr 2018 to the primary completion date, Dec 2027
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Recent recipient of any licensed or investigational live attenuated vaccine(s) within 4 weeks of transplant.
Other illness
- Patients who have underlying malignant conditions.
- Patients who have non-malignant conditions not requiring BMT.
- HIV positive by serology or PCR, HTLV positive by serology. If HTLV serology is positive, it will be confirmed by nucleic acid testing (NAT). If HTLV NAT is negative, subject will remain eligible regardless of HTLV serology result.
- 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 infection, as determined by the appropriate imaging and/or confirmatory testing e.g. blood cultures, PCR testing, etc.
Lab values
- 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.
Other
- 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.
- Females who are pregnant or who are lactating.
Who the study is looking for
- Individuals must meet all of the following criteria in order to be eligible for this study.
- Subject must be able to understand and provide informed consent.
- Male or female, 18 through 60 years old, inclusive, at the time of informed consent.
- Meet criteria for UNOS listing for lung transplantation.
- Patients must have evidence of end stage lung disease. Examples of such diseases include but are not limited to:
- Pulmonary Fibrosis
- COPD/Emphysema
- Patients must have evidence of bone marrow failure with abnormal low cell count in at least one hematopoietic line, making the patient a poor candidate for long-term immunosuppressive therapy. Eligible patients must meet at least one of the following criteria:
- Unexplained, non-drug induced neutropenia with absolute neutrophils counts of \<1500/µL the previous year, confirmed by repeat testing
- Unexplained, non-drug induced thrombocytopenia with mean platelets counts of \<100,000/µL the previous year, confirmed by repeat testing
- Unexplained, non-hemolytic anemia, with a hemoglobin level of \< 12 g/dL the previous year, confirmed by repeat testing
- GFR ≥45 mL/min/1.73 m2.
- AST, ALT ≤4x upper limit of normal, total bilirubin ≤ 2.5 mg/dL, normal INR, albumin \>3.0 g/dL
- Cardiac ejection fraction ≥ 40% or shortening fraction ≥26%.
- Negative pregnancy test for females, 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 will also be counseled regarding the potential risks of infertility following BMT and advised to discuss sperm banking or oocyte harvesting.
Age in the registry: 18 years to 60 years · Sex: All · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| UPMC Presbyterian Coordinator of this site? Confirm its status | Pittsburgh | United States | Recruiting |
| Children's Hospital of Pittsburgh of UPMC Coordinator of this site? Confirm its status | Pittsburgh | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.