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NCT04271800

Safety and Efficacy of CD19-Targeted CAR-T Therapy for Relapsed/Refractory CD19+ B Cell Leukemia and Lymphoma

Status unknown Phase 1, PHASE2 Last updated 18 April 2023
What this trial tests

Phase 1, PHASE2 trial testing CD19 CAR-T cells in Leukemia in 40 participants. Status unknown.

Timeline
1 December 2019
Primary endpoint
31 December 2023
1 July 2024

Quick facts

Lead sponsorChongqing Precision Biotech Co., Ltd
PhasePhase 1, PHASE2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment40
Start date1 December 2019
Primary completion31 December 2023
Estimated completion1 July 2024
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Chongqing Precision Biotech Co., Ltd — full company profile →

Who can join

Adults 3 to 75, any sex, with Leukemia or Lymphoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a single arm study to evaluate the efficacy and safety of CD19-targeted CAR-T cells therapy for patients with relapsed/refractory CD19+ B Cell Leukemia and Lymphoma.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Immune Dysfunctions and Immune-Based Therapeutic Interventions in Chronic Lymphocytic Leukemia.
    Griggio V, Perutelli F, Salvetti C, Boccellato E, et al · · 2020 · cited 54× · PMID 33312177 · DOI 10.3389/fimmu.2020.594556

Verify or expand the search:

Other trials of CD19 CAR-T cells

Trials testing the same drug.

Other recruiting trials for Leukemia

Currently open trials in the same condition.

Other Chongqing Precision Biotech Co., Ltd trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04271800.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing