Stem cell transplant offers new hope for rare immune diseases
NCT ID NCT07284641
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a stem cell transplant for people with common variable immunodeficiency (CVID) and other immune disorders. The goal is to replace the faulty immune system with a healthy donor's stem cells. Participants are aged 5 to 40 and will receive a reduced-intensity transplant. The main outcome is survival, and the study is currently recruiting.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 25 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2026
- Expected to finish
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Feb 2031
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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5 to 40 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Patient, parent, or legal guardian must have given written informed consent. For pediatric subjects who are developmentally able, assent or affirmation will be obtained. 2. Male or female, 5 through 40 years old, inclusive, at the time of informed consent. 3. Patients must have evidence of common variable immunodeficiency (CVID) or other autoimmune manifestation of a primary immune regulatory disorder (PIRD). Genetic screening is required by a targeting gene panel to determine presence of genetic variations that may lead to inborn errors of immunity. Examples of such diseases include, but are not limited to: * Common variable immunodeficiency (CVID) * Combined Immunodeficiency (CID) * Immune dysregulation polyendocrinopathy enteropathy X-linked (IPEX syndrome), IPEX like syndromes * Combined immunodeficiency with defects in T-cell-mediated immunity, including Omenn syndrome and DiGeorge Syndrome * Chronic Granulomatous Disease (CGD) * Signal Transducer and Activator of Transcription (STAT 1) Gain of Function (STAT1 GOF) * Signal Transducer and Activator of Transcription (STAT 3) Gain of Function (STAT3 GOF) * Hypomorphic Recombination-Activating Genes (RAG) 1 and RAG 2 * CD40 or CD40L deficiency * Mendelian Susceptibility to Mycobacterial Disease * GATA-binding factor 2 (GATA2) Associated Immunodeficiency * Mouth and Genital Ulcers with Inflamed Cartilage Syndrome (MAGIC) 4. Must have previously failed, due to lack of response or intolerance, mycophenolate mofetil and a B cell-depleting antibody, such as Rituximab 5. Glomerular Filtration Rate (GFR) ≥50 mL/min/1.73 m2 6. Aspartate Aminotransferase (AST) ≤4x upper limit of normal 7. Alanine Aminotransferase (ALT) ≤4x upper limit of normal 8. Direct bilirubin ≤ 2.5 mg/dL 9. Human Immunodeficiency Virus (HIV) negative by serology and PCR 10. Human T-cell Lymphotropic Virus (HTLV) negative by serology 11. Cardiac ejection fraction ≥ 40% or shortening fraction ≥26% 12. Forced Vital Capacity (FVC) and Forced Expiratory Volume in 1 second (FEV1) ≥40% predicted for age 13. Peripheral Capillary Oxygen Saturation (SpO2) of \>92% at rest on room air 14. Subjects must be a minimum of 8 weeks post-solid organ transplant prior to start of conditioning, if applicable 15. Negative pregnancy test for females \>10 years old or who have reached menarche, unless surgically sterilized. 16. All females of childbearing potential and sexually active males must agree to use a FDA approved method of birth control for up to 12 months after stem cell transplant or for as long as they are taking any medication that may harm a pregnancy, an unborn child or may cause birth defects. 17. Subject and/or parent guardian informed of the potential risks of infertility following stem cell transplant and advised to discuss sperm banking or oocyte harvesting. 18. Transplant endorsement from clinical immunologist Exclusion Criteria: 1. Allergy to Dimethylsulfoxide (DMSO) or any other ingredient used in the manufacturing of the stem cell product 2. Uncontrolled systemic infection, as determined by the appropriate confirmatory testing e.g. blood cultures, Polymerase chain reaction (PCR) testing, etc. 3. Recent recipient of any licensed or investigational live attenuated vaccine(s) within 4 weeks of stem cell transplant 4. 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 subject's ability to comply with study requirements or that may impact the quality or interpretation of the data obtained from the study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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UPMC Children's Hospital of Pittsburgh
RECRUITINGPittsburgh, Pennsylvania, 15224, United States
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Other studies related to the condition(s) this trial covers.
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