ClinicalTrials.gg
RecruitingNCT05932173Updated Jul 11, 2023

A Study of Novel Anti-CD19 CAR-T in Patients With r/r B-Cell Malignancies

A Phase 1/2 interventional study of Anti-CD19 Autologous CAR-T Cell Infusion in B-Cell Leukemia, B-Cell Lymphoma and B-cell Tumors, sponsored by 920th Hospital of Joint Logistics Support Force of People's Liberation Army of China. Recruiting at 1 site in China. Open to participants aged 2 Years to 75 Years. Per ClinicalTrials.gov, last updated 2023-07-11.

Sponsored by 920th Hospital of Joint Logistics Support Force of People's Liberation Army of China · Phase 1/2, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Jun 2024, 2 years 4 months ago, but the record still lists the study as recruiting.
  • Started Jul 2023; still recruiting 3 years 4 months later.
Phase
Phase 1/2
Study type
Interventional
Enrollment
60
Allocation
Not applicable
Ages
2 Years to 75 Years
Sex
All
01

Study summary

It is a single-center, open-labeled, single-arm, non-randomized, investigator-initiated trial aiming to evaluate the efficacy and safety of anti-CD19 CAR-T manufactured by OlyCAR platform (OlyCAR-019) for CD19+ refractory/relapsed B-Cell malignancies.

Read the detailed description

OlyCAR is a novel CAR-T manufacturing system which allows to generate clinical-use CAR-T cells in short time. This study is going to evaluate the feasibility of CAR-T manufactured by OlyCAR platform in the treatment of B-Cell malignancies. The OlyCAR-019 cells will be infused by vein. Subjects will be followed for safety and efficacy up to 12 weeks. For those with a durable remission 12 weeks after infusion, the follow-up will last for at least 12 months for disease control.

02

Conditions studied

  • B-Cell Leukemia
  • B-Cell Lymphoma
  • B-cell Tumors

Keywords

  • B Cell
  • CAR-T
  • CD19
  • Leukemia
  • Lymphoma
03

In context

Leukemia, B-Cell

190 studies on the registry are indexed under Leukemia, B-Cell; 52 are open to participants now.

This study's planned enrollment of 60 is above the median of 39 across 162 interventional studies indexed under Leukemia, B-Cell.

Browse Leukemia, B-Cell studies →

Lead sponsor

920th Hospital of Joint Logistics Support Force of People's Liberation Army of China is the lead sponsor of 18 studies on the registry; 10 are open to participants now.

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

04

Who can participate

Ages eligible
2 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Key Inclusion Criteria:

  1. A definite diagnosis of B-cell ;
  2. Male or female, aged 2-75 years;
  3. Confirmed detectable disease;
  4. Expected survival time >12 weeks;
  5. (ECOG) score is 0-2;
  6. Adequate liver , kidney and cardiopulmonary function;
  7. Women of childbearing age have negative blood pregnancy test before the start of the trial, and agree to take effective measures during the trial until the last follow-up; male subjects with partners of agree to take effective contraceptive measures during the trial until the last follow-up;
  8. Willingness to complete the process and to comply with study procedures and visit schedule.

Key Exclusion Criteria:

  1. Presence of other concurrent active malignancy; People with severe mental disorders;
  2. History of any of the following genetic disorders, such as Fanconi anemia, Schu-Day syndrome, Gerstmann syndrome, or any other known bone marrow failure syndrome;
  3. Acute of grade II-IV or extensive chronic GVHD;
  4. Grade III-IV heart failure or myocardial infarction, cardiac angioplasty or stenting, unstable angina pectoris, or other clinically prominent heart disease within one year prior to enrollment;
  5. The presence of any indwelling catheter or drainage (e.g., percutaneous nephrostomy, indwelling catheter, bile drainage, or pleural/peritoneal/pericardial catheter), except for patients who are permitted to use dedicated central venous catheters;
  6. (HIV) seropositivity; surface antigen positive or hepatitis B core antibody positive, and HBV-DNA positive; Patients with (HCV-RNA quantitative test results positive); Or the presence of other serious active viral or bacterial infections or uncontrolled systemic fungal infections; Patients with severe history of allergy or allergic constitution;
  7. A history of diseases (e.g., Crohn's disease, rheumatoid arthritis, systemic lupus erythematosus) leading to end-organ damage or requiring systemic /systemic disease modulating drugs within the past 2 years; Had or is suffering from interstitial lung disease (e.g., pneumonia, pulmonary fibrosis);
  8. Had undergone other clinical trials in the 4 weeks prior to participating in this trial;
  9. Poor compliance due to physiological, family, social, geographical and other factors, unable to cooperate with the study protocol and follow-up plan;
  10. For patients with cyclophosphamide and fludarabine chemotherapy;
  11. Subjects requiring systemic therapy (prednisone ≥5mg/ day or equivalent dose of another corticosteroid) or other immunosuppressive agents within 1 month after UCAR-T cell reinfusion, except for adverse events;
  12. Receiving donor lymphocyte infusion within 6 weeks before enrollment;
  13. Pregnant and lactating women;
  14. Subjects with any other condition which the investigator considers unsuitable for inclusion in the study.
Terms in these criteria, in plain language(14)

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.

Relapsed and refractory

Relapsed: the illness came back after treatment had worked. Refractory: it did not respond to treatment, or stopped responding while still on it.

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.

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.

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.

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.

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.

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.

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 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.

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.

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.

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.

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.

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.

05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    OlyCAR-019 Cell Infusion

    OlyCAR-019 cell infusion will be administered by vein after short-time manufacture.

    Biological: Anti-CD19 Autologous CAR-T Cell Infusion

Interventions

  • BiologicalAnti-CD19 Autologous CAR-T Cell Infusion

    Autologous T cells modified with anti-CD19 ScFv expression and manufactured by OlyCAR platform

    Also known as: OlyCAR-019

06

What researchers measure

Primary outcomes

  1. Incidence of adverse events(AE) after infusion

    The frequency, severity, and laboratory findings of all adverse events/serious adverse events are included.

    Time frame: Up to 12 months after infusion

  2. MTD

    MTD will be determined based on DLTs observed during the first 28 days of study treatment.

    Time frame: Up to 28 days after infusion

Secondary outcomes

  1. Overall Response Rate (ORR)

    Overall Response Rate (ORR) is defined as the proportion of subjects achieving complete remission(CR) and partial response(PR).

    Time frame: Up to 3 months after infusion

  2. Progression-free survival(PFS)

    Progression-free survival(PFS) refers to the time from cell infusion to the first assessment of tumor progression or death from any cause.

    Time frame: Up to 3 months after infusion

07

Study locations

1 of 1 sites recruiting
  • 920th Hospital of Joint Logistics Support Force of People's Liberation Army of China
    Kunming, Yunnan 650100, China
    Recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jul 2023 (actual). Primary completion is estimated for Jun 2024, 11 months after the start.

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

Registered
Jun 27, 2023
First posted
Jul 6, 2023
StartActual
Jul 1, 2023
Primary completionEst.
Jun 30, 2024
CompletionEst.
Jun 30, 2025
Last update
Jul 11, 2023
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 Jul 11, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05932173
Lead sponsor
920th Hospital of Joint Logistics Support Force of People's Liberation Army of China
Responsible party
Sponsor
First posted
Jul 6, 2023
Start date
Jul 1, 2023
Primary completion
Jun 30, 2024 (estimated)
Completion
Jun 30, 2025 (estimated)
Last update
Jul 11, 2023

Study contacts

Sanbin Wang, Professor
Contact
Sanbin1011@163.com
13187424131 ext. +86
Shiqi Li, MD
Contact
Lystch@qq.com
15398671578
Sanbin Wang, Professor
principal investigator · 920th Hospital of Joint Logistics Support Force of People's Liberation Army of China

Oversight

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

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