ClinicalTrials.gg
RecruitingNCT07524816Updated Apr 13, 2026

Real World Practice With Academic Anti CD19 CAR-T Cell Therapy in Relapse/Refractory B-cell Lymphoma

An observational study in Large B-Cell Lymphoma (LBCL), sponsored by N.N. Alexandrov National Cancer Centre. Recruiting at 1 site in Belarus. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-04-13.

Sponsored by N.N. Alexandrov National Cancer Centre · Observational

From the registry’s dates

  • Started Jun 2021; still recruiting 5 years 5 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
76
Ages
18 Years to 80 Years
Sex
All
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Study summary

Chimeric antigen receptor (CAR) T-cell therapy has been the standard of care for relapsed/refractory large B-cell lymphomas (R/R LBCLs) since 2018. However, high cost of commercial products limits their application in real-world clinical practice. Academic approach to manufacturing CAR-T cell products can reduce the costs and improve availability and affordability of this therapy option. The aim of the present study is assess the efficacy and safety of the use of academic CAR-T cell products in r/r LBCL patients.This prospective observational study with r/r LBCL patients treated in the NN Alexandrov National Cancer Centre of Belarus. The CAR-T cell product was manufactured using lentiviral vector encoding anti-CD19 CAR.

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Conditions studied

  • Large B-Cell Lymphoma (LBCL)

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Keywords

  • academic CAR-T cell products
  • r/r large B-cell lymphomas
  • efficacy
  • safety
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In context

Lymphoma, B-Cell

885 studies on the registry are indexed under Lymphoma, B-Cell; 286 are open to participants now.

This study's planned enrollment of 76 is below the median of 150 across 69 observational studies indexed under Lymphoma, B-Cell.

Browse Lymphoma, B-Cell studies →

Lead sponsor

N.N. Alexandrov National Cancer Centre is the lead sponsor of 5 studies on the registry; 5 are open to participants now.

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

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Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

patients with relapse or refractiry LBCL treated in N.N. Alexandron National Cancer Center

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

  • age ≥18 years,
  • LBCL,
  • confirmed CD19 expression in tumor tissue,
  • prior exposure to at least one line of anti-tumor therapy

Exclusion criteria

Exclusion Criteria:

  • pregnancy,
  • active or C infection, infection,
  • naïve T-lymphocyte count (CD3+CCR7+5RO-) ≤ 0,5%
Terms in these criteria, in plain language(4)

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.

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.

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.

CD4 count

The number of CD4 cells, a type of white blood cell, in a given amount of blood. It is used to follow how well the immune system is doing in HIV.

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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
76 participants (estimated)
Target follow-up
3 Months
Patient registry
Yes

Interventions

  • OtherCAR-T cell therapy

    The academic CAR-T cell product presented in this study encodes the anti-CD19 CAR construct with the single-chain variable fragment (scFv) of an anti-CD19 monoclonal antibody (FMC63) conjugated with the CD8 hinge region, CD4-1BB transmembrane (TM), co-stimulatory domain, and the CD3ζ pro-activator signaling domain along with a truncated form of the epidermal growth factor receptor (EGFRt) cell surface protein as a co-expression marker and a safety switch mechanism.

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What researchers measure

Primary outcomes

  1. ORR

    metabolic response evaluated by 2-deoxy-\[18F\]-fluoro-D-glucose positron emission tomography/computed tomography (FDG-PET/CT) performed on day 30 post-infusion

    Time frame: day 30 post-infusion

Secondary outcomes

  1. event-free survival (EFS)

    was defined as the time from CAR T-cell infusion to disease progression, relapse, or death from any cause, whichever occurred first; patients alive without events were censored at the last follow-up

    Time frame: 5 years

  2. Overall survival

    was calculated from the date of infusion to the date of death or last follow-up.

    Time frame: 5 years

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Study locations

1 of 1 sites recruiting
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References and documents

Publications

  • Katsin M, Dormeshkin D, Meleshko A, Migas A, Dubovik S, Konoplya N. CAR-T Cell Therapy for Classical Hodgkin Lymphoma. Hemasphere. 2023 Nov 16;7(12):e971. doi: 10.1097/HS9.0000000000000971. eCollection 2023 Dec. PubMed 38026793 ↗
  • Konoplya NE, Doroshenko TM, Zharkova KY, Savich TV, Seviaryn IM, Bobrova NM, Beleevsky AA, Sarydze EK, Polyakov SL. Academic anti CD19 CAR-T cell therapy for relapsed/refractory B-cell lymphomas in real-world clinical practice: a prospective cohort study. Front Oncol. 2026 Jul 17;16:1862517. doi: 10.3389/fonc.2026.1862517. eCollection 2026. PubMed 42539439 ↗

Related links

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: Undecided

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07524816
Lead sponsor
N.N. Alexandrov National Cancer Centre
Responsible party
Sponsor
First posted
Apr 13, 2026
Start date
Jun 1, 2021
Primary completion
Jan 1, 2028 (estimated)
Completion
Jan 1, 2029 (estimated)
Last update
Apr 13, 2026

Study contacts

Natalya Konoplya, PhD, MD, Professor
Contact
NKonoplya@mail.ru
+375297723101

Oversight

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

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