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A Safety Study of Autologous T Cells Engineered to Target CD19 and CRISPR Gene Edited to Eliminate Endogenous HPK1 (XYF19 CAR-T Cells) for Relapsed or Refractory Haematopoietic Malignancies.
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Aug 04, 2026
Report code
NCT04037566-Aug 04, 2026
NCT ID
NCT04037566
Status
UNKNOWN
Phase
Phase 1
Sponsor
Xijing Hospital
Executive brief
Investment-Ready Snapshot
The XYF19 CAR-T cell therapy targets CD19, a well-established antigen in B cell malignancies, and employs CRISPR technology to enhance therapeutic efficacy by eliminating endogenous HPK1. This first-in-human trial is positioned in a competitive landscape dominated by existing CAR-T therapies, particularly those targeting CD19, such as Kymriah and Yescarta. The trial's focus on relapsed or refractory cases, particularly in patients not eligible for HSCT, addresses a significant unmet medical need. Successful outcomes could position Xijing Hospital and its collaborator, Xi'An Yufan Biotechnology Co., Ltd, favorably in the CAR-T market, which is projected to grow significantly, driven by increasing incidences of hematological malignancies and advancements in gene editing technologies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04037566
Indication
Leukemia Lymphocytic Acute (ALL) in Relapse
Modality
cell therapy
Target
CD19 and endogenous HPK1 (CRISPR gene edited)
Intervention
XYF19 CAR-T cell, Cyclophosphamide, Fludarabine
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.