ClinicalTrials.gg
Status unknownNCT04204161Updated Feb 4, 2021

A Clinical Study of CAR-T Cells Treatment for Children With CD19+/CD22+ R/R ALL and Lymphoma

A Phase 1 interventional study of CAR-T19/CAR-T22 in Relapsed B-cell Acute Lymphoblastic Leukemia, Childhood, Refractory B-cell Acute Lymphoblastic Leukemia, Childhood and Relapsed/Refractory B-cell Lymphoma, Childhood, sponsored by Shenzhen BinDeBio Ltd.. Status unknown at 1 site in China. Open to participants aged 1 Month to 18 Years. Per ClinicalTrials.gov, last updated 2021-02-04.

Sponsored by Shenzhen BinDeBio Ltd. · Phase 1, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Feb 2021), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 1
Study type
Interventional
Enrollment
30
Allocation
Not applicable
Ages
1 Month to 18 Years
Sex
All
01

Study summary

This is a single arm, open-label, uni-center, phase I study . In this study, Children withCD19+/CD22+ R/R B-cell acute lymphoblastic leukemia or lymphoma will be treated with CAR-T19/CAR-T22 Immunotherapy to determine the safety and efficacy of treatment.

02

Conditions studied

  • Relapsed B-cell Acute Lymphoblastic Leukemia, Childhood
  • Refractory B-cell Acute Lymphoblastic Leukemia, Childhood
  • Relapsed/Refractory B-cell Lymphoma, Childhood
03

In context

Burkitt Lymphoma

976 studies on the registry are indexed under Burkitt Lymphoma; 159 are open to participants now.

This study's planned enrollment of 30 is below the median of 36 across 765 interventional studies indexed under Burkitt Lymphoma.

Browse Burkitt Lymphoma studies →

Lead sponsor

Shenzhen BinDeBio Ltd. is the lead sponsor of 6 studies on the registry; none are open to participants now.

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

04

Who can participate

Ages eligible
1 Month to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Male and female subjects with CD19+/CD22+ B cell who have limited prognosis (several months to \< 2 year survival) with currently available therapies will be enrolled.

    1. no available curative treatment options (such as or allogeneic SCT)
    2. If patients had receive immunotherapy, they should reach requirments:tumor recurrency or the number of B cells recovered.
    3. Patients with recurrence after hematopoietic stem cell transplantation need additional satisfaction: 1) no GvHD and not require ;2) stem cell transplantation was completed for at least 4 months, and at least 6 months before the CART reinfusion;
    4. Patients must be willing to sign an .
    5. Age:≤18 years.
    6. survival>12 weeks
    7. Flow cytometry or IHC showed positive expression of CD19/ CD22 in tumor cells within two months.
    8. Routine blood test:>=90 g/L; >=50×10\^9/L.
    9. Liver function: and AST≤2.5 () times the upper limits of normal (if abnormal liver function is mainly caused by tumor infiltration, it can ≤5 ULN), \<2.0 mg/dl.
    10. Renal function:BUN: 9-20mg / dl; serum creatinine\<= 1.5 times upper limits of normal; endogenous rate>=50 ml/min
    11. Negative serum antibody for EBV, CMV, , syphilis, HBVa nd .
    12. Cardiac function: stable hemodynamic and (LVEF)>=55%.
    13. score ≤2。
    14. Adequate venous access for apheresis, and no other for leukapheresis

Exclusion criteria

Exclusion Criteria:

  1. >= 3.
  2. Patients with history of T cell tumors .
  3. organ failure:heart failure Ⅲ and Ⅳ;The liver reached grade C of child-turcotte .Renal failure and uremia;Respiratory failure;People with impaired consciousness.
  4. Acute or chronic after allogeneic hematopoiesis. Hormone or was used within 30 days.
  5. hormoneswere used before and after blood collection and infusion.
  6. infection or active or infection.
  7. Uncontrolled active infection.
  8. Enrolled to other clinical study in the last 4 weeks.
  9. Subjects with systemic auto-immune disease or immunodeficiency.
  10. Allergic to cytokines.
  11. Definite neuropathic or psychotic patients, including authors of dementia or seizures, history of psychotropic substance abuse and unable to quit, or other substantial lesions that may increase central neurotoxicity.
  12. Patients with malignant tumors of the central nervous system.
  13. Lung, brain or intestinal tumor infiltrates.
  14. The second tumor was found.
  15. Allergic to cytokine antagonists.
  16. Other patients that researchers considered unsuitable for inclusion.
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.

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.

Allogeneic and autologous transplant

Stem cell (bone marrow) transplants. Allogeneic uses cells from a donor; autologous uses your own cells, collected earlier and given back.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

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.

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).

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.

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.

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.

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.

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.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

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.

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.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

GVHD (graft-versus-host disease)

After a transplant from a donor, the donor’s immune cells attack the recipient’s body, often the skin, gut or liver.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

05

Study design

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

Study arms

  • Experimental
    CAR-T19/CAR-T22

    CAR-T19/CAR-T22 (autologous T cells transduced with CD19 / 22 CAR-ζ/4-1BB vector) will be administered to children with R/R B cell Acute Lymphoblastic Leukemia (ALL) or Lymphoma as an IV infusion on days 0, 1 and 2 in the absence of disease progression or unacceptable toxicity.

    Biological: CAR-T19/CAR-T22

Interventions

  • BiologicalCAR-T19/CAR-T22

    According to tumor burden and other conditions, patients will be treated with cyclophosphamide or fludarabine,then,CAR-T cells will be infused 48-72 hours later.The recommand dose is 1x10\^5/kg-2.5x10\^8/kg .

06

What researchers measure

Primary outcomes

  1. Number of Participants With Adverse Events evaluated with NCI CTC AE, version 4.0

    Safety evaluation

    Time frame: 60 months

Secondary outcomes

  1. Overall remission rate

    Overall remission rate consists of complete remission rate and partial remission rate of patients being treated with CAR-T19/CAR-T22

    Time frame: 60 months

  2. CAR-T cells testing

    The level of CAR-T cells will be tested regularly by Real-time Quantitative Polymerase Chain Reaction Detecting System(qPCR) or Flow cytometry to evaluate the proliferation in vivo and long-term survival.

    Time frame: 60 months

07

Study locations

1 of 1 sites recruiting
  • Xiangya Hospital Central South University
    Changsha, Hunan 410008, China
    Recruiting
    • Yang Minghua, PhD · Contact13973135843
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Oct 2019 (actual). Primary completion is estimated for Oct 2021, 24 months after the start.

Of 109 phase 1 interventional studies under Burkitt Lymphoma, half reached primary completion within 61 months of starting (the median), counting those still running; a quarter within 38 and three quarters within 90. This study's planned 24 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 13, 2019
First posted
Dec 18, 2019
StartActual
Oct 8, 2019
Primary completionEst.
Oct 30, 2021
CompletionEst.
Oct 8, 2024
Last update
Feb 4, 2021
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 4, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04204161
Lead sponsor
Shenzhen BinDeBio Ltd.
Responsible party
Sponsor
First posted
Dec 18, 2019
Start date
Oct 8, 2019
Primary completion
Oct 30, 2021 (estimated)
Completion
Oct 8, 2024 (estimated)
Last update
Feb 4, 2021

Study contacts

Yang Zhonghua
Contact
zh.yang@bindebio.com
18938688105
Yang Zhonghua
study director · Shenzhen BinDeBio Tech Co.,Ltd

Oversight

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

Not currently enrolling

This study is status unknown, as verified in Feb 2021. You cannot join it, but the record below documents what was studied.

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