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A Clinical Study to Investigate Safety, Tolerability, and Preliminary Efficacy of mRNA Encoding CD19/CD3 T Cell Engager (ABO2203) in Adult Patients With Relapsed or Refractory B-NHL
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT07072169-Jul 28, 2026
NCT ID
NCT07072169
Status
RECRUITING
Phase
PHASE1
Sponsor
Ruijin Hospital
Executive brief
Investment-Ready Snapshot
A Clinical Study to Investigate Safety, Tolerability, and Preliminary Efficacy of mRNA Encoding CD19/CD3 T Cell Engager (ABO2203) in Adult Patients With Relapsed or Refractory B-NHL is a PHASE1 clinical asset sponsored by Ruijin Hospital in B-cell Non-Hodgkin Lymphoma. SEO and diligence focus: ABO2203 Injection, endpoint relevance, enrollment feasibility, competitive positioning, readout timing and IP durability.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT07072169
Indication
B-cell Non-Hodgkin Lymphoma
Modality
small molecule
Target
ABO2203 Injection
Intervention
ABO2203 Injection
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.