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Nanobody-Based CD19/CD20 Tandem Dual CAR-T-Cell Therapy for Relapsed/Refractory B-Cell Lymphoma Early Phase 1

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Summary

NIH registered a new Early Phase 1 clinical trial (NCT07546630) evaluating the safety and efficacy of Nanobody-Based CD19/CD20 Tandem Dual CAR-T-cell therapy for the treatment of relapsed/refractory B-cell lymphoma. The single-arm study will assess this novel tandem dual-targeting approach. This registration provides public visibility into an investigational CAR-T cell therapy program targeting both CD19 and CD20 antigens simultaneously.

“This is a single arm study to evaluate the safety and efficacy of Nanobody-Based CD19/CD20 Tandem Dual CAR-T-cell therapy for Relapsed/Refractory B-Cell Lymphoma”

NIH , verbatim from source
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About this source

ClinicalTrials.gov is the NIH-run registry of every clinical trial conducted in the United States, plus most international trials sponsored by US-based companies or institutions. By federal law, sponsors must register Phase 2 through Phase 4 studies before enrolling patients and post results within a year of completion. This feed tracks every new trial registration and study update, around 700 a month: drug interventions, device studies, behavioral protocols, observational research. Watch this if you scout drug candidates moving into mid or late-stage development, monitor competitor pipelines, or follow rare disease research where new trials signal patient hope. GovPing parses sponsor, phase, intervention, and target indication on each entry.

What changed

NIH published a new Early Phase 1 clinical trial registration (NCT07546630) for a nanobody-based CD19/CD20 tandem dual CAR-T cell therapy targeting relapsed/refractory B-cell lymphoma. The single-arm study will evaluate both safety and preliminary efficacy of this dual-targeted approach. This registration makes the trial publicly available on ClinicalTrials.gov, fulfilling requirements for transparency in human subjects research. For pharmaceutical companies and clinical investigators developing CAR-T or other cellular therapy programs, this registration illustrates the continued exploration of multi-antigen targeting strategies in hematologic malignancies. Sponsors and investigators should ensure all applicable clinical trial registrations are current and accurately reflect protocol amendments.

Archived snapshot

Apr 24, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← ClinicalTrials.gov Studies

Nanobody-Based CD19/CD20 Tandem Dual CAR-T-cell Therapy of Relapsed/Refractory B-Cell Lymphoma

Early Phase 1 NCT07546630 Kind: EARLY_PHASE1 Apr 23, 2026

Abstract

This is a single arm study to evaluate the safety and efficacy of Nanobody-Based CD19/CD20 Tandem Dual CAR-T-cell therapy for Relapsed/Refractory B-Cell Lymphoma

Conditions: Relapsed/Refractory B-Cell Lymphoma

Interventions: CD19/CD20 Tandem Dual CAR-T

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Last updated

Classification

Agency
NIH
Published
April 23rd, 2026
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor

Who this affects

Applies to
Clinical investigators Pharmaceutical companies
Industry sector
3254.1 Biotechnology
Activity scope
Clinical trial registration Cellular therapy development
Geographic scope
United States US

Taxonomy

Primary area
Pharmaceuticals
Operational domain
Regulatory Affairs
Topics
Healthcare Biotechnology

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