Last update 22 Jun 2026

BRL-301

Overview

Basic Info

Drug Type
Universal CAR-T
Synonyms
Anti CD19 universal chimeric antigen receptor T cell therapy(Shanghai Bioray Laboratory), CD19UCART, Universal CD19 CAR-T(Shanghai Bioray Laboratory)
+ [4]
Target
Action
inhibitors
Mechanism
CD19 inhibitors(B-lymphocyte antigen CD19 inhibitors), Immunologic cytotoxicity, T lymphocyte replacements
Inactive Indication-
Originator Organization
Active Organization
Inactive Organization-
License Organization-
Drug Highest PhasePhase 1
First Approval Date-
Regulation-
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Aggressive B-Cell Non-Hodgkin LymphomaPhase 1
China
16 Mar 2026
Acute Lymphoblastic LeukemiaPhase 1-20 Dec 2023
B-Cell LymphomaPhase 1-20 Dec 2023
Non-Hodgkin LymphomaPhase 1-20 Dec 2023
Precursor B-Cell Lymphoblastic Leukemia-LymphomaPhase 1-20 Dec 2023
Rheumatic DiseasesClinical
China
15 Jul 2024
Autoimmune DiseasesClinical--
Systemic Lupus ErythematosusIND Approval
China
20 Sep 2025
B-cell lymphoma refractoryIND Approval
China
17 Apr 2025
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Phase 1/2
5
dlsnobgoka(hetqssknjk) = included cytopenias attributable to lymphodepletion hkkqbgedby (fhisaypfxl )
Positive
29 May 2026
Phase 1
4
(Allogeneic CD19-targeted CAR-T Therapy)
rzpfqvxnlt(codhfxcdul) = The most commonly observed grade 3 or 4 adverse events (AEs) within the first few weeks included neutropenia, lymphopenia and fatigue, which were considered relatively to the lymphodepletion conditioning regimen. All of them developed grade 1 CRS for 2 or 3 days, which recovered soon without tocilizumab and steroid usage. No ICANS and GvHD observed in all subjects. dwdhuvtsbe (itmfzffvab )
Positive
13 May 2026
Not Applicable
4
heeexibuqu(prgxaxrpna) = The most commonly observed grade 3 or 4 adverse events within the first few weeks were neutropenia, lymphopenia, hepatic dysfunction, fever, and fatigue. Neutropenia and lymphopenia were attributed to the lymphodepletion conditioning regimen. All patients experienced only grade 1 cytokine release syndrome (CRS), manifesting as fever that persisted for 2–3 days. No patients developed immune effector cell-associated neurotoxicity syndrome (ICANS) or GVHD during treatment. irxebncxsf (hauqdrermi )
Positive
08 May 2025
Not Applicable
3
cdanacarhe(odvtdnpmfy) = the significant improvement in the clinical response index scores for the two diseases, respectively, and supported by the observations of reversal of inflammation and fibrosis. ejqejeyknn (xgauelwfnn )
Positive
15 Jul 2024
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Regulation

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