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Clinical trial intelligence report
Study of Safety and Efficacy of Anti-CD19 Chimeric Antigen Receptor T Cell(C-CAR011) Treatment in Subjects With Relapsed or Refractory B Cell Non-Hodgkin Lymphoma
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT03154775-Jul 28, 2026
NCT ID
NCT03154775
Status
UNKNOWN
Phase
Phase 1
Sponsor
Shanghai AbelZeta Ltd.
Executive brief
Investment-Ready Snapshot
C-CAR011, developed by Shanghai AbelZeta Ltd., targets CD19 for the treatment of relapsed or refractory B cell Non-Hodgkin Lymphoma (NHL). The asset is positioned in a competitive landscape dominated by established CAR-T therapies such as Kymriah (tisagenlecleucel) and Yescarta (axicabtagene ciloleucel). Given the increasing prevalence of NHL and the unmet need for effective therapies in relapsed cases, C-CAR011 could capture market share if it demonstrates superior efficacy or safety profiles. The trial's single-arm design and focus on a specific patient population may streamline regulatory pathways, but the commercial viability will depend on the robustness of clinical outcomes and pricing strategies in comparison to existing therapies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03154775
Indication
Refractory or Relapsed Non-Hodgkin Lymphoma
Modality
cell therapy
Target
CD19 (Chimeric Antigen Receptor T Cell Therapy)
Intervention
C-CAR011
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.