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OncoMatch/Clinical Trials/NCT07779018

CD19/CD22 CAR-T Consolidation in R/R Aggressive B-Cell Lymphoma After Second-Line Therapy

Is NCT07779018 recruiting? Yes, currently enrolling (Sep 2026). This Phase 2 trial studies CD22/CD19 CAR-T cell immunotherapy for lymphoma.

Phase 2RecruitingLiping DouNCT07779018Data as of Sep 2026Location: China

Treatment: CD22/CD19 CAR-T cell immunotherapyThe purpose of this study is to determine the efficacy and safety of CD22/CD19-targeted CAR-T cell immunotherapy as consolidation therapy after second-line treatment in patients with high-risk aggressive B-cell lymphoma.

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Extracted eligibility criteria

Treatments studied

Other

CD22/CD19 CAR-T cell immunotherapy

Cancer type

Non-Hodgkin Lymphoma

Hodgkin Lymphoma

Diffuse Large B-Cell Lymphoma

Primary Central Nervous System Lymphoma

Biomarker criteria

Required: CD19 expression (positive)

CD19 and/or CD22-positive large B-cell lymphoma (LBCL)

Required: CD22 expression (positive)

CD19 and/or CD22-positive large B-cell lymphoma (LBCL)

Allowed: MYC rearrangement

FISH confirmed high-grade B-cell lymphoma with double or triple strikes, accompanied by MYC and BCL2 and/or BCL6 rearrangements

Allowed: BCL2 rearrangement

FISH confirmed high-grade B-cell lymphoma with double or triple strikes, accompanied by MYC and BCL2 and/or BCL6 rearrangements

Allowed: BCL6 rearrangement

FISH confirmed high-grade B-cell lymphoma with double or triple strikes, accompanied by MYC and BCL2 and/or BCL6 rearrangements

Allowed: MYC expression

Immunohistochemistry suggests dual expression of MYC and BCL-2 (recommended dual expression threshold is MYC ≥ 40%, BCL2 ≥ 50%)

Allowed: BCL2 expression

Immunohistochemistry suggests dual expression of MYC and BCL-2 (recommended dual expression threshold is MYC ≥ 40%, BCL2 ≥ 50%)

Allowed: CD5 expression

Immunohistochemical CD5 positivity

Allowed: TP53 mutation

Gene sequencing shows TP53 mutation

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Ages ≤ 85

Prior therapy

Must have received: second-line chemotherapy — induction treatment

disease has achieved complete response (CR) after induction treatment with a standard second-line chemotherapy regimen

Cannot have received: CAR-T cell therapy

Have received any form of chimeric antigen receptor cell therapy or other genetically modified T cell therapy

Lab requirements

Blood counts

HGB ≥ 60g/L; absolute neutrophil count ≥ 1000/μl; platelet count ≥ 45000/μl

Kidney function

Serum creatinine ≤ 1.5x ULN or creatinine clearance rate ≥ 60 mL/min

Liver function

Total bilirubin (TBIL) ≤ 1.5x ULN (except Gilbert's syndrome); ALT/AST ≤ 2.5x ULN

Cardiac function

LVEF ≥ 50%; ECHO confirms no pericardial effusion and no clinically significant arrhythmia

Liver and kidney function, as well as heart and lung function, meet the following requirements: 1) Total bilirubin (TBIL) ≤ 1.5 times the upper limits of normal (ULN), except for subjects with Gilbert's syndrome; 2) Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5 times ULN; 3) Serum Creatinine (Cr) ≤ 1.5 times ULN or Creatinine Clearance Rate (CCr) ≥ 60mL/min, estimated based on the Cockcroft Gault formula; 4) The left ventricular ejection fraction (LVEF) of the heart is ≥ 50%. Echocardiography (ECHO) confirms no pericardial effusion and no clinically significant arrhythmia; 5) Baseline transcutaneous oxygen saturation under indoor ventilation>92%; 6) No clinically significant pleural effusion

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT07779018 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior CAR-T cell therapy disqualifies patients from enrollment.

Does this trial require CD19?

Yes, CD19 expression is a required biomarker for enrollment.

Does this trial require CD22?

Yes, CD22 expression is a required biomarker for enrollment.

Is there an age limit?

Yes. Patients must be 85 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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