Recruiting
Phase 1
Phase 2

Lentiviral Gene Transfer

Sponsor:

David Williams

Code:

NCT03311503

Conditions

Severe Combined Immunodeficiency, X Linked

Gene Therapy

Eligibility Criteria

Sex: Male

Age: 0 - 5

Healthy Volunteers: Not accepted

Interventions

autologous CD34+ cell transduced with G2SCID vector

Study Details

Brief summary:

This is a phase I/II open label multi-center study in which patients will receive low dose targeted busulfan followed by infusion of autologous CD34+ selected bone marrow or mobilized peripheral blood cells transduced with the G2SCID vector. Subjects will be enrolled over 3 years and be followed for 2 years post-infusion on this protocol, then followed long-term on a separate long-term follow-up protocol.

Enrollment of subjects will be agreed upon by representatives of both sites. Data will be collected uniformly from both sites through an electronic capture system and key laboratory studies will be centralized.

Harvest, cellular manufacturing and infusion will occur at each site using the same SOPs. Key aspects of cellular product characterization will be centralized

Conditions

Severe Combined Immunodeficiency, X Linked

Gene Therapy

Study ID

NCT03311503

Start date

Feb 26, 2018

Status verified date

Dec, 2025

Completion date

Jan 1, 2028

Anticipated

Primary completion date

Jan 1, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Male

Age: 0 - 5

Healthy Volunteers: Not accepted

Inclusion Criteria:

\- 1. Diagnosis of SCID-X1 based on immunophenotype and lack of T cell function (proliferation to PHA <10% of the lower limit of normal for the laboratory) AND confirmed by a mutation in IL2RG 2. Lack of an HLA identical (A, B, C, DR, DQ) related donor 3. Age 5 years old or younger 4. Signed informed consent 5. Documentation of willingness to follow up for 15 years post-infusion as currently required by the FDA 6. If the patient has previously undergone allogeneic transplant, lack of donor T cell engraftment must be documented.

7\. Age at least 8 weeks by the time of busulfan administration

Exclusion Criteria:

1. Patients with an active, therapy-resistant infection. Infections that are known to be highly morbid in SCID patients will be considered active and therapy-resistant if the infectious agent is repeatedly isolated despite a minimum of 2 weeks of appropriate therapy and is associated with significant organ dysfunction (including but not limited to abnormalities listed below).

1. Mechanical ventilation including continuous positive airway pressure
2. Abnormal liver function defined by AST and ALT >10 times the upper range of normal OR Bilirubin >2 mg/dL
3. Shortening fraction on echocardiogram <25% or ejection fraction <50%
4. Renal failure defined as glomerular filtration rate <30 ml/min/1.73 m2 or dialysis dependence
2. Uncontrolled seizure disorder
3. Encephalopathy
4. Documented coexistence of any disorder known to affect DNA repair
5. Diagnosis of active malignant disease other than EBV-associated lymphoproliferative disease
6. Patients with evidence of infection with HIV-1
7. Major (life-threatening) congenital anomalies. Examples of "major (life-threatening) congenital anomalies" include, but are not limited to: unrepaired cyanotic heart disease, hypoplastic lungs, anencephaly or other major central nervous system malformations, other severe non-repairable malformations of the gastrointestinal or genitourinary tracts that significantly impair organ function.
8. Other conditions which in the opinion of the P.I. or co-investigators, contra-indicate collection and/or infusion of transduced cells or indicate patient's inability to follow the protocol. These may include for example clinical ineligibility to receive anesthesia, severe deterioriation of clinical condition of the patient after collection of bone marrow but before infusion of transduced cells, or documented refusal or inability of the family to return for scheduled visits. There may be other unforeseen rare circumstances that would result in exclusion of the patient, such as sudden loss of legal guardianship

\-

Study Design

Enrollment

12 participants

Anticipated

Allocation

Non randomized

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Treatment arm

single infusion of autologous CD34+ cells transduced with the self-inactivating (SIN) lentiviral vector G2SCID

Interventions

autologous CD34+ cell transduced with G2SCID vector

single infusion of autologous CD34+ cells transduced with the self-inactivating (SIN) lentiviral vector G2SCID

Primary outcome measure

  • The primary objective is to measure event free survival [ Time Frame: 1 year post infusion ]
  • T cell reconstitution [ Time Frame: 1 year post infusion ]

Central Contacts and Locations

Locations

Mattel Children's Hospital - UCLA

Recruiting

Los Angeles, California, United States, 90095

Contacts

Donald Kohn, MD

(310) 825-6708

Emory University/Childrens Healthcare of Atlanta

Recruiting

Atlanta, Georgia, United States, 30322

Contacts

Principal Investigator:

Shanmuganathan Chandrakasan, MD

Boston Childrens Hospital

Recruiting

Boston, Massachusetts, United States, 02115

Contacts

Principal Investigator:

Susan Prockop, MD

Cincinnati Children's Hospital Medical Center

Recruiting

Cincinnati, Ohio, United States, 45229

Contacts

Principal Investigator:

Sharat Chandra, M.D.

More Information

Sponsor

David Williams

Last update posted

Dec 11, 2025

Last verified

Dec, 2025

Keywords

  • lentiviral
  • Gene therapy
  • busulfan

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by David Williams on 2025-12-11.