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NCT Number: NCT04661020

CD19 CAR-T Therapy for Patients With Newly Diagnosed High-risk Large B-cell Lymphoma

A Study of CD19 CAR-T Therapy for Patients With Newly Diagnosed High-risk Large B-cell Lymphoma

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

The First Affiliated Hospital,College of Medicine, Zhejiang University

Hangzhou, Zhejiang, 310003, China

Location status: Recruiting

Location contact

He Huang, PhD

CONTACT

[email protected]

86-13605714822

About this study

This study is indicated for patients with CD19+ newly diagnosed high-risk large B-cell lymphoma. This study is an investigator-initiated, single-center, single-arm phase II clinical trial of rituximab, lenalidomide, and zanubrutinib (ZR2) with Sequential CAR-T cell as first-line therapy for newly diagnosed high-risk LBCL. Primary objective is to explore the efficacy and also safety.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age no less than 18, no gender limit;
  • Newly diagnosed high-risk Large B-cell Lymphoma, which was defined by the following criteria: (1) DLBCL not otherwise specified with an IPI score ≥3 at diagnosis, (2) high grade B-cell lymphoma (HGBL) with gene rearrangement of MYC and BCL2 and/or BCL6, (3) HGBL not otherwise specified;
  • Confirmed CD19 and CD20 postive expressions in lymphoma cells
  • ECOG score 0-2;
  • Total bilirubin ≤ 51 umol/L, ALT and AST ≤ 3 times of upper limit of normal, creatinine ≤ 176.8 umol/L;
  • Echocardiogram shows left ventricular ejection fraction (LVEF) ≥50%;
  • No active infection in the lungs, blood oxygen saturation in indoor air is ≥ 92%;
  • Estimated survival time ≥ 3 months;
  • Patients or their legal guardians volunteer to participate in the study and sign the informed consent.

Exclusion criteria

  • Central nervous system involvement by lymphoma;History of craniocerebral trauma, conscious disturbance, epilepsy, cerebrovascular ischemia, and cerebrovascular, hemorrhagic diseases;
  • Electrocardiogram shows prolonged QT interval, severe heart diseases such as severe arrhythmia in the past;
  • Patients with severe active infections (excluding simple urinary tract infection and bacterial pharyngitis);
  • Active infection of hepatitis B virus or hepatitis C virus;
  • Previously treated with any CAR-T cell product or other genetically modified T cell therapies;
  • Insufficient amplification capacity in response to CD3/CD28 co-stimulus signal (<5 times) ;
  • Other uncontrolled diseases that were not suitable for this trial;
  • Patients with HIV infection;
  • Any situations that the investigator believes may increase the risk of patients or interfere with the results of study.

Treatment and study plan

CD19 CAR-T cells

Drug

Each subject receive CD19 CAR T-cells by intravenous infusion

Other names: CD19 CAR-T cells injection

Primary outcomes

  1. Complete remission rate after CD19 CAR-T cell therapy

    Time frame: 3 months after CD19 CAR-T cell therapy

    Assessment of complete remission rate at 3 months after CD19 CAR-T cell therapy

Secondary outcomes

  1. Overall response rate (ORR)

    Time frame: After ZR2, 3 months after CAR-T cell therapy

    Assessment of ORR after ZR2 and CAR-T cell therapy

  2. Overall survival (OS)

    Time frame: Up to 2 years after CD19 CAR-T cells infusion

    From the start of treatment to death or the last visit

  3. Progression-free survival (PFS)

    Time frame: Up to 2 years after CD19 CAR-T cells infusion

    From the start of the treatment to the occurrence of any event, including death, disease progression (any one occurs first), or the last visit

  4. Duration of response (DOR)

    Time frame: Up to 2 years after CD19 CAR-T cells infusion

    among patients experiencing an objective response, defined as the time from the first objective response to events of disease progression or death from any cause

  5. Incidence of treatment-emergent adverse events (TEAEs)

    Time frame: Up to 2 years after CD19 targeted CAR T-cells infusion

    Incidence of treatment-emergent adverse events [Safety and Tolerability]

Study contacts

Contact information is provided by the study sponsor or research team.

He Huang, PhD

CONTACT

[email protected]

86-13605714822

Yongxian Hu, PhD

CONTACT

[email protected]

86-15957162012

Sponsors and collaborators

Lead sponsor

Zhejiang University

Other

Collaborators

  • Yake Biotechnology Ltd.

Registry information

Official study title

Clinical Trial for the Efficacy and Safety of CD19 CAR-T Therapy for Patients With Newly Diagnosed High-risk Large B-cell Lymphoma

Important dates

Study start
2020
Primary completion
2026
Study completion
2026
First posted
Dec 9, 2020
Registry last updated
Apr 7, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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