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RecruitingNCT05210907Updated Feb 6, 2023

Clinical Study of Hospital-manufactured CD19 CAR-T in Children and Adolescents With Acute Lymphoblastic Leukemia

A Phase 1 interventional study of SNUH-CD19-CAR-T in B-cell Acute Lymphoblastic Leukemia, sponsored by Seoul National University Hospital. Recruiting at 1 site in Korea, Republic of. Open to participants aged 0 Years to 25 Years. Per ClinicalTrials.gov, last updated 2023-02-06.

Sponsored by Seoul National University Hospital · Phase 1, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Sep 2025, 1 year ago, but the record still lists the study as recruiting.
  • Started Feb 2022; still recruiting 4 years 7 months later.
Phase
Phase 1
Study type
Interventional
Enrollment
5
Allocation
Not applicable
Ages
0 Years to 25 Years
Sex
All
01

Study summary

Chimeric antigen receptor T cells (CAR-T cells) have been developed to treat relapsed and refractory hematological malignancies with promising outcome in patients with very poor prognosis. The purpose of this clinical study is to produce the CD19[cluster of differentiation antigen 19] CAR-T (SNUH-CD19-CAR-T) at the investigational site and to evaluate safety and efficacy of SNUH-CD19-CAR-T in children and adolescent with relapsed/refractory B-cell acute lymphoblastic leukemia.

02

Conditions studied

03

In context

Leukemia

5,441 studies on the registry are indexed under Leukemia; 636 are open to participants now.

This study's planned enrollment of 5 is below the median of 38 across 4,247 interventional studies indexed under Leukemia.

Browse Leukemia studies →

Lead sponsor

Seoul National University Hospital is the lead sponsor of 1,860 studies on the registry; 275 are open to participants now.

Of its 12 completed or terminated interventional studies of FDA-regulated products, 2 (17%) have results posted.

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

04

Who can participate

Ages eligible
0 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

    1. Relapsed or refractory CD19 Positive Acute Lymphoblastic Leukemia. All subjects must be younger than 26 years old at the time of obtaining informed consent

      a. 2nd or greater BM[bone marrow] relapse OR b. Any BM relapse after allogeneic SCT[stem cell transplant] and must be ≥ 6 months from SCT at the time of SNUH_CD19_CAR-T infusion OR c .Refractory as defined by not achieving a CR after 2 cycles of a standard chemotherapy regimen or chemorefractory as defined by not achieving a CR after 1 cycle of standard chemotherapy for relapsed leukemia OR d. Ineligible for allogeneic SCT because of:

      • Severe comorbid disease
      • Other contraindications to allogeneic SCT conditioning regimen
      • Lack of suitable donor

        1. Documentation of CD19 tumor expression in bone marrow or peripheral blood by flow cytometry.
        1. Karnofsky (age ≥ 16 years) or Lansky (age \< 16 years) performance status ≥ 50 at screening

Exclusion criteria

Exclusion Criteria:

  1. Evidence of uncontrolled hepatitis B virus (HBV) or hepatitis C virus (HCV) based on assessment done by treating physicians.
  2. Known human immunodeficiency virus (HIV) infection.
  3. Presence of clinically active uncontrolled infection based on assessment done by treating physicians. Infections are considered controlled if appropriate therapy has been instituted and, at the time of screening, no signs of progression are present. Persisting fever without other signs or symptoms will not be interpreted as progressing infection.
  4. Pregnant or nursing (lactating) women.
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
5 participants (estimated)

Study arms

  • Experimental
    CD19 CAR-T therapy

    SNUH-CD19-CAR-T is administered as an intravenous infusion.

    Biological: SNUH-CD19-CAR-T

Interventions

  • BiologicalSNUH-CD19-CAR-T

    SNUH-CD19-CAR-T is an autologous CAR-T from T cells collected from each patient. Administer a single dose of SNUH-CD19-CAR-T to patients with relapsed or refractory CD19 positive B-cell acute lymphoblastic leukemia, and evaluate safety and efficacy of SNUH-CD19-CAR-T for 12 months after the infusion.

06

What researchers measure

Primary outcomes

  1. Incidence of adverse events and its severity

    Time frame: 12 months post SNUH-CD19-CAR-T infusion

Secondary outcomes

  1. Patients with CR[complete remission] after Hospital-manufactured CAR-T infusion

    Time frame: 1 month post SNUH-CD19-CAR-T infusion

  2. Overall survival and event-free survival

    Time frame: 12 months post SNUH-CD19-CAR-T infusion

07

Study locations

1 of 1 sites recruiting
  • Seoul National University Hospital
    Seoul, 03080, Korea, Republic of
    • Hyoung Jin Kang, MD, PhD · Contact
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 6, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05210907
Lead sponsor
Seoul National University Hospital
Responsible party
Sponsor
First posted
Jan 27, 2022
Start date
Feb 15, 2022
Primary completion
Sep 30, 2025 (estimated)
Completion
Aug 31, 2026 (estimated)
Last update
Feb 6, 2023

Study contacts

Hyoungjin Kang, PhD
Contact
kanghj@snu.ac.kr
+82-2-2072-3304

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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