ClinicalTrials.gg
RecruitingNCT02579967Updated Nov 5, 2026

Pilot Trial of Allogeneic Blood or Marrow Transplantation for Primary Immunodeficiencies

A Phase 2 interventional study of Immunosuppression Only Conditioning -Closed with amendment L and Reduced Intensity Conditioning in Primary T-cell Immunodeficiency Disorders, Common Variable Immunodeficiency and Immune System Diseases, sponsored by National Cancer Institute (NCI). Recruiting at 2 sites in United States. Open to participants aged 4 Years to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-05.

Sponsored by National Cancer Institute (NCI) · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Started Nov 2015; still recruiting 10 years 11 months later.
Phase
Phase 2
Study type
Interventional
Enrollment
354
Allocation
Non-randomized
Ages
4 Years to 75 Years
Sex
All
01

Study summary

Background:

Allogeneic blood or marrow transplant is when stem cells are taken from one person s blood or bone marrow and given to another person. Researchers think this may help people with immune system problems.

Objective:

To see if allogeneic blood or bone marrow transplant is safe and effective in treating people with primary immunodeficiencies.

Eligibility:

Donors: Healthy people ages 4 or older

Recipients: People ages 4-75 with a primary immunodeficiency that may be treated with allogeneic blood or marrow transplant

Design:

Participants will be screened with medical history, physical exam, and blood tests.

Participants will have urine tests, EKG, and chest x-ray.

Donors will have:

Bone marrow harvest: With anesthesia, marrow is taken by a needle in the hipbone.

OR

Blood collection: They will have several drug injections over 5-7 days. Blood is taken by IV in one arm, circulates through a machine to remove stem cells, and returned by IV in the other arm.

Possible vein assessment or pre-anesthesia evaluation

Recipients will have:

Lung test, heart tests, radiology scans, CT scans, and dental exam

Possible tissue biopsies or lumbar puncture

Bone marrow and a small piece of bone removed by needle in the hipbone.

Chemotherapy 1-2 weeks before transplant day

Donor stem cell donation through a catheter put into a vein in the chest or neck

Several-week hospital stay. They will take medications and may need blood transfusions and additional procedures.

After discharge, recipients will:

Remain near the clinic for about 3 months. They will have weekly visits and may require hospital readmission.

Have multiple follow-up visits to the clinic in the first 6 months, and less frequently for at least 5 years.

Read the detailed description

Background:

  • Primary immunodeficiency diseases (PIDs) are conditions associated with major quantitative or qualitative immunologic abnormalities that are, in most cases, due to defects in cells of hematopoietic origin
  • Participants with PID can have life-threatening complications including malignancy, recurrent infection, and autoimmunity/immune dysregulation
  • Allogeneic blood or marrow transplantation (allo BMT) has the potential to cure the immune defect in PID and thereby reduce the morbidity and mortality associated with these diseases

Objectives:

-To estimate the acute graft-versus-host disease (aGVHD)-free, graft failure-free survival at day +180 after allo BMT, analyzed separately by conditioning arm/cohort

Eligibility:

  • Patients age >= 4 through 75 years
  • PID deemed to be of sufficient past severity to warrant allo BMT, by meeting the two criteria below:

    • PID as defined by identified genetic defect or, in the absence of a mutation, patients with an immune defect potentially amenable to allo BMT who meet the clinical history criteria below may be eligible
    • Clinical history of at least two of the following:

      • Life-threatening, organ-threatening, or severely disfiguring infection
      • Protracted or recurrent infections
      • Infection with an opportunistic organism
      • Chronic elevation in the blood of a latent virus
      • Evidence of immune dysregulation
      • Hypogammaglobulinemia/dysglobulinemia
      • Hematologic malignancy or lymphoproliferative disorder
      • Virus-associated solid tumor malignancy or pre-cancerous lesion
  • At least one 7-8/8 (9-10/10) HLA-matched related or unrelated donor, or an HLA-haploidentical related donor
  • Adequate end-organ function
  • Consensus opinion by the investigative team that the patient has the potential to benefit from transplant despite existing, non-hematopoietic organ dysfunction
  • Not pregnant or breastfeeding
  • HIV negative
  • Disease status: patients with malignancy should be referred in remission for evaluation, except in the case of virus-associated malignancy who may be referred at any time

Design:

  • The study will have two arms that vary in mycophenolate mofetil (MMF) duration.
  • RIC and RIC-MMF arms: pentostatin 4 mg/m2/day IV on days -11 and -7, low-dose cyclophosphamide orally daily on days -11 through -4; busulfan IV, pharmacokinetically dosed, on days -3 and -2.
  • RIC-SHORT arm: pentostatin 4 mg/m2/day IV on days -9 and -5, low-dose cyclophosphamide orally daily on days -9 through -2; busulfan IV, pharmacokinetically dosed, on days -3 and -2.
  • Bone marrow is the preferred graft source. Peripheral blood stem cells are permitted on RIC-MMF arm but not on RIC-SHORT arm.
  • GVHD prophylaxis:

    • High-dose, post-transplantation cyclophosphamide (PTCy) on days +3 and +4, sirolimus on days +5 through +90, and mycophenolate mofetil (MMF) on days +5 through +35 for all arms except the RIC-MMF and RIC-SHORT arm. The RICMMF arm will receive MMF of varying durations based on a duration de-escalation schema.
    • RIC-SHORT: Reduced-dose, post-transplantation cyclophosphamide (PTCy) on days +3 and +4, sirolimus on days +5 through +90, and mycophenolate mofetil (MMF) on days +5 through +18.
02

Conditions studied

  • Primary T-cell Immunodeficiency Disorders
  • Common Variable Immunodeficiency
  • Immune System Diseases
  • Autoimmune Lymphoproliferative
  • Lymphoproliferative Disorders

Keywords

  • Haploidentical
  • Autoimmunity
  • Immune Dysregulation
  • Congenital
  • Opportunistic Infection
03

In context

Common Variable Immunodeficiency

54 studies on the registry are indexed under Common Variable Immunodeficiency; 13 are open to participants now.

This study's planned enrollment of 354 is above the median of 40 across 39 interventional studies indexed under Common Variable Immunodeficiency.

Browse Common Variable Immunodeficiency studies →

Lead sponsor

National Cancer Institute (NCI) is the lead sponsor of 3,556 studies on the registry; 336 are open to participants now.

Of its 411 completed or terminated interventional studies of FDA-regulated products, 373 (91%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
4 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

  • INCLUSION CRITERIA - RECIPIENT:
  • Patients age >= 4 through 75 years
  • PID deemed to be of sufficient past severity to warrant allo BMT, by meeting the two criteria below:

    1. PID as defined by identified genetic defect or, in the absence of a PID-associated genetic mutation, patients with an immune defect potentially amenable to allo BMT who meet the clinical history criteria below may be eligible upon discussion with the PI

      • Mutations should be confirmed in a CLIA-certified laboratory, if such testing is available.
      • Patients without a mutation must be deemed eligible and appropriate for allo BMT by the PI. Some patients may meet the clinical history criteria listed below, but will not be eligible if it is thought that their clinical history is due to a condition apart from an immune defect. In addition, patients with a PID of mild severity, such as those with selective IgA deficiency, may meet at least two of the clinical history criteria, but may be deemed inappropriate for allo BMT by the PI if it is felt that the risks of the procedure outweigh the severity of the disease.
    2. Clinical history of at least two of the following:

      • Life-threatening, organ-threatening, or severely disfiguring infection
      • Protracted or recurrent infections requiring unusually long or repeated courses of antibiotics
      • Infection with an opportunistic organism
      • Chronic elevation in the blood (>=2 documented elevations over a period of 6 months or longer) of a latent virus (EBV, CMV, HHV6, HHV8, etc.)
      • Evidence of immune dysregulation, as manifested by disease, atopy, hemophagocytic lymphohistiocytosis/macrophage activation syndrome, granulomas, splenomegaly, or lymphadenopathy
      • Patients with hemophagocytic lymphohistiocytosis or macrophage activation syndrome related to an underlying lymphoma with no other clinical history suggestive of a primary immunodeficiency will not be eligible
      • Hypogammaglobulinemia, dysglobulinemia, or impaired response to vaccination
      • Hematologic or lymphoproliferative disorder
      • Tissue diagnosis should be confirmed by NCI Department of Pathology, if prior are available
      • Virus-associated solid tumor malignancy or pre-cancerous lesion
      • Tissue diagnosis should be confirmed by NCI Department of Pathology, if prior biopsies are available
  • Availability of at least one 7-8/8 (9-10/10) HLA-matched related (excluding an identical twin) or unrelated donor, or an HLA-haploidentical related donor
  • Consensus among the PI, key AIs, and consultants (as necessary) that correction of the patient s immune system through BMT has the potential to improve the patient s health, quality of life, and/or , after taking into consideration the patient s existing non-hematopoietic, potentially irreversible organ dysfunction
  • Adequate end-organ function, as measured by:

    • (LVEF) >= 40% by 2D echocardiogram (ECHO) or MUGA, or left ventricular shortening fraction >= 20% by ECHO for patients receiving RIC or RIC-MMF, or RIC-SHORT, or LVEF >= 30% if the patient has radiologic evidence of aortic, renal, or coronary artery vasculitis.
    • Pulmonary function tests: DL(co) (corrected for ) and FEV(1) >= 40% of predicted for the RIC, RIC-MMF, and RIC-SHORT arms; or in pediatric patients, if unable to perform pulmonary function tests, there should be no evidence of dyspnea at rest, no requirement for supplemental oxygen, and oxygen saturation >92% on room air. Calculations will be based on the values reported in CRIS.
    • \<= 3.0 mg/dL (unless due to Gilbert s syndrome or hemolysis) for patients receiving RIC, RIC-MMF, RIC-SHORT; and AST 10 x for patients receiving RIC, RIC-MMF, RIC-SHORT. Patients who are above these bilirubin, ALT, or AST thresholds may be eligible for the RIC, RIC-MMF, or RIC-SHORT arms if evaluated by a hepatologist who deems the liver function test abnormalities to be potentially reversible with bone marrow transplant.
    • Estimated of >= 40 mL/min/1.73 m\^2, calculated using the Cockcroft-Gault equation for adults and Schwartz formula for pediatric patients, for patients with creatinine levels above the institutional upper limit of normal
  • or Lansky performance status of >=60% or performance status of 2 or less
  • Ability of subject or Legally Authorized Representative (LAR) to understand and the willingness to sign a written document
  • Not pregnant or breastfeeding. As therapeutic agents used in this trial may be harmful to a fetus, women of and men must agree to use adequate (hormonal or barrier method of birth control; abstinence) prior to study entry and for at least one year post-allo BMT. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in the study, she should inform her treating physician immediately.
  • Disease status: Patients with malignancy are to be referred in remission for evaluation, except in cases of virus-associated malignancy who may be referred at any time. Should a patient have progressive disease or a donor becomes unavailable after enrollment, the patient will be referred back to his/her primary hematologist-oncologist for treatment. If this course of action is not in the best interest of the patient according to the clinical judgment of the PI, then the patient may receive standard treatment for the malignant disease under the current study, although this should only occur as a bridge to transplant. If under either of these settings, it becomes apparent that the patient will not be able to proceed to transplant, then he/she must come off the study. Patients receiving standard therapy will be told about the therapy, associated risks, potential benefits, alternatives to the proposed therapy, and the availability of receiving the same treatment elsewhere, outside of a research protocol.

EXCLUSION CRITERIA - RECIPIENT:

  • Patients who are receiving any other agents, with the exception of virus-specific cytotoxic T-cells for the treatment of viral infection/reactivation prior to allo BMT.
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to agents (cyclophosphamide, busulfan, pentostatin, sirolimus, MMF, filgrastim or filgrastim biosimilar) used in the study
  • Active psychiatric disorder which may compromise compliance with the transplant protocol, or which does not allow for appropriate informed consent
  • Active central nervous system (CNS) involvement by malignancy, except in cases of virus-associated malignancies with CNS involvement in which case the patient may benefit from the transplant to control the malignancy.
  • MAGT1 mutation and active need to take anti- agents and/or therapeutic anti-coagulation that cannot be interrupted during aplasia.
  • positive or other acquired immunodeficiency that, as determined by the PI, interferes with the assessment of PID severity and/or the attribution of clinical manifestations of immunodeficiency to a PID.
  • Lack of adequate central venous access potential

Inclusion Criteria (Related Donor):

  • Ages >= 4
  • Related donor deemed suitable and eligible and willing to donate per clinical evalations who are additionally willing to donate blood, urine, and marrow specimens for research. Related donors will be evaluated in accordance with existing Standard Policies and Procedures for determination of eligibility and suitability for clinical donation. Note that participation in this study is offered to all related donors but is not required for clinical donation, so it is possible that not all related donors will enroll on this study.

Exclusion Criteria (Related Donor):

None

INCLUSION CRITERIA - UNRELATED DONOR:

  • Ages >= 18
  • Unrelated donors will be evaluated in accordance with existing NMDP Standard Policies and Procedures, available at: http://bethematch.org/About-Us/Global-transplant-network/Standards/, except for the additional requirement of EBV serostatus testing. Note that participation in this study is offered to all unrelated donors but not required for clinical donation, so it is possible that not all unrelated donors will enroll on this study.

EXCLUSION CRITERIA - UNRELATED DONOR:

-Unrelated donors: failure to qualify as a National Marrow Donor Program (NMDP) donor per current NMDP Standards, available at: http://bethematch.org/About-Us/Global-transplant-network/Standards/.

Terms in these criteria, in plain language(18)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Biopsy and archival tissue

A biopsy takes a small piece of tissue to examine. “Archival tissue” is a sample already taken, for example at diagnosis, and kept by the hospital.

Whether a stored sample will do depends on when it was taken, how much there is and what the study needs. Ask whether the study accepts your stored sample or needs a new biopsy.

Life expectancy

The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.

LVEF (left ventricular ejection fraction)

The share of blood the heart’s main pumping chamber (the left ventricle) pushes out with each beat, measured by an echocardiogram (heart ultrasound) or a MUGA scan. About 50–70% is normal.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

Creatinine clearance (CrCl)

How quickly the kidneys clear creatinine, a waste product, from the blood. A study may estimate it from a blood test with age, weight and sex (often by the Cockcroft–Gault formula), or measure it using blood and urine collected over a set time. Given in mL/min; higher is better.

Karnofsky performance status (KPS)

A 0–100 scale of how well someone can carry out everyday activities. 100 is no complaints and no signs of illness; 70 is able to look after yourself but not to work or keep up normal activity; 50 is needing considerable help and frequent medical care.

Studies often ask for 60 or 70 and above. Your doctor gives the score.

ECOG performance status

A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
354 participants (estimated)

Study arms

  • Experimental
    1/ IOC Arm-Closed with amendment L (07/05/2019)

    Immunosuppression Only Conditioning Arm

    Drug: Immunosuppression Only Conditioning -Closed with amendment L · Drug: GVHD Prophylaxis · Procedure: Allo BMT

  • Experimental
    2/ RIC Arm - Closed with Amendment L (07/05/2019)

    Reduced Intensity Conditioning Arm

    Drug: Reduced Intensity Conditioning · Drug: GVHD Prophylaxis · Procedure: Allo BMT

  • Experimental
    3/ MAC Arm-Closed with amendment L (07/05/2019)

    Myeloablative Conditioning Arm

    Drug: Myeloablative Conditioning-Closed with amendment L · Drug: GVHD Prophylaxis · Procedure: Allo BMT

  • Experimental
    4/ RIC-MMF Arm

    Reduced Intensity Conditioning with MMF duration de-escalation design

    Drug: Reduced Intensity Conditioning · Drug: GVHD Prophylaxis · Procedure: Allo BMT

  • No intervention
    5/ Donor Arm

    Donor

  • Experimental
    6/ RIC-SHORT Arm

    Reduced Intensity Conditioning with shortened duration and dose-reduced PTCy

    Drug: Reduced Intensity Conditioning · Drug: GVHD Prophylaxis · Procedure: Allo BMT

Interventions

  • DrugImmunosuppression Only Conditioning -Closed with amendment L

    Pentostatin 4 mg/m2/day IV on days -9 and -5, cyclophosphamide 5 mg/kg orally daily on days -9 through -2 (Closed with amendment L)

  • DrugReduced Intensity Conditioning

    pentostatin 4 mg/m2/day IV on days -11 and -7, cyclophosphamide 3 mg/kg orally daily on days -11 through -4; busulfan IV, pharmokinetically dosed, on days -3 and -2.

  • DrugMyeloablative Conditioning-Closed with amendment L

    Pentostatin 4 mg/m2/day IV on days -13 and -9, low-dose cyclophosphamide orally daily on days -13 through -6; busulfan IV, pharmokinetically dosed, on days -5, -4, -3, and -2. (Closed with amendment L)

  • DrugGVHD Prophylaxis

    High-dose, post-transplantation cyclophosphamide (PTCy) 25-50 mg/kg on days +3 and +4, sirolimus 6 mg on days +5 through +90, and mycophenolate mofetil (MMF) on days +5 through 0, +18, +25, or +35 depending on treatment arm and cohort.

  • ProcedureAllo BMT

    Allogeneic blood or marrow transplantation

06

What researchers measure

Primary outcomes

  1. For the RIC-SHORT arm: To estimate the aGVHD-free, graft failure-free survival

    Proportion of participants without GVHD

    Time frame: +180 after allo BMT

  2. For the RIC : To estimate the aGVHD-free, graft failure-free survival

    Proportion of participants without GVHD

    Time frame: +180 after allo BMT

  3. For the RIC-MMF arm: To determine the shortest duration of MMF that can be safely administered without excessive rates of graft failure or acute grade 3-4 GVHD

    Shortest duration of MMF

    Time frame: Duration de-escalation design

Secondary outcomes

  1. Transplant-related mortality

    Cumulative incidence of transplant-related mortality at 180 days and 1 year post transplant.

    Time frame: +180 and 1 year post transplant

  2. Secondary graft failure

    Cumulative incidence of secondary graft failure at 1 year post transplant.

    Time frame: 1 year post transplant

  3. Overall survival

    Time from transplant to death of any cause.

    Time frame: 1 year post transplant

  4. Kinetics and durability of lineage-specific donor chimerism

    Median amount of patient who has early chimerism

    Time frame: days +28 and +42

  5. Kinetics and durability of engraftment

    The percentage of donor T-, B-, NK-, and myeloid cell populations at days +28, +42, +60, +100, +180, and 1 year post transplant.

    Time frame: days +28, +42, +60, +100, +180, and 1 year after allo BMT

  6. Incidence of Chronic Graft-versus-host disease

    Cumulative incidence of chronic graft versus host disease at 1 and 2 years post transplant.

    Time frame: 1 and 2 years post transplant

  7. Incidence of Acute Graft-versus-host disease

    Cumulative incidence of acute graft versus host disease at 1 year post transplant

    Time frame: 1 year post transplant

  8. Event-free survival

    Time from transplant to death of any cause or other event, including disease relapse, graft failure, grade 3-4 acute GVHD, chronic GVHD requiring systemic therapy, or receipt of post-transplant donor cell infusion.

    Time frame: 1 year post transplant

  9. Disease free survival

    Time from transplant to death of any cause or disease relapse.

    Time frame: 1 year post-transplant

07

Study locations

2 of 2 sites recruiting
  • National Institutes of Health Clinical Center
    Bethesda, Maryland 20892, United States
    Recruiting
    • For more information at the NIH Clinical Center contact National Cancer Institute Referral Office · Contact888-624-1937
  • National Marrow Donor Program
    Minneapolis, Minnesota 55413-1753, United States
    Recruiting
08

References and documents

Publications

  • Bashey A, Zhang X, Sizemore CA, Manion K, Brown S, Holland HK, Morris LE, Solomon SR. T-cell-replete HLA-haploidentical hematopoietic transplantation for hematologic malignancies using post-transplantation cyclophosphamide results in outcomes equivalent to those of contemporaneous HLA-matched related and unrelated donor transplantation. J Clin Oncol. 2013 Apr 1;31(10):1310-6. doi: 10.1200/JCO.2012.44.3523. Epub 2013 Feb 19. PubMed 23423745 ↗
  • Mariotti J, Taylor J, Massey PR, Ryan K, Foley J, Buxhoeveden N, Felizardo TC, Amarnath S, Mossoba ME, Fowler DH. The pentostatin plus cyclophosphamide nonmyeloablative regimen induces durable host T cell functional deficits and prevents murine marrow allograft rejection. Biol Blood Marrow Transplant. 2011 May;17(5):620-31. doi: 10.1016/j.bbmt.2010.11.029. Epub 2010 Dec 3. PubMed 21130889 ↗
  • Kang E, Gennery A. Hematopoietic stem cell transplantation for primary immunodeficiencies. Hematol Oncol Clin North Am. 2014 Dec;28(6):1157-70. doi: 10.1016/j.hoc.2014.08.006. Epub 2014 Sep 16. PubMed 25459185 ↗

Individual participant data

Plan to share: Yes — All IPD recorded in the medical record will be shared with intramural investigators upon request. In addition, all large scale genomic sequencing data will be shared with subscribers to dbGAP

Supporting information: Study protocol, Statistical analysis plan, Informed consent form

Time frame: Clinical data available during the study and indefinitely. Genomic data are available once genomic data are uploaded per protocol GDS plan for as long as the database is active.

Access criteria: Clinical data will be made available and with permission of the study PI. Genomic data are made available via dbGAP through requests to the data custodians

09

Updates

6 registry updates since Sep 25, 2026
Minor edits
Nothing that changes what the study is or who can join. Edited: description, verification date and references
6 updates, last Nov 5, 2026
Show all 6 updates
  1. Nov 5, 2026
    Minor edits only
    + 1 other change: verification date
  2. Nov 3, 2026
    Minor edits only
    + 1 other change: description
  3. Oct 26, 2026
    Minor edits only
    + 1 other change: description
  4. Oct 21, 2026
    Minor edits only
    + 1 other change: verification date
  5. Oct 16, 2026
    Minor edits only
    + 2 other changes: verification date and references
  6. Sep 28, 2026
    Minor edits only
    + 1 other change: description

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT02579967
Responsible party
Sponsor
First posted
Oct 20, 2015
Start date
Nov 19, 2015
Primary completion
Dec 31, 2031 (estimated)
Completion
Dec 31, 2036 (estimated)
Last update
Nov 5, 2026

Study contacts

Amy H Chai
Contact
amy.chai@nih.gov
(240) 858-3755
Dimana Dimitrova, M.D.
Contact
dimana.dimitrova@nih.gov
(240) 858-3647
Dimana Dimitrova, M.D.
principal investigator · National Cancer Institute (NCI)

Oversight

FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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