TrialSignal
Clinical trial intelligence report
Multicenter, Single-Arm Exploratory Phase I Clinical Study on the Safety and Efficacy of Fully Human BAFF-R Chimeric Antigen Receptor T-Cell Injection in Participants With Relapsed/Refractory BAFF-R-Positive B-Cell Lymphoma
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT07259070-Jul 28, 2026
NCT ID
NCT07259070
Status
RECRUITING
Phase
PHASE1
Sponsor
Institute of Hematology & Blood Diseases Hospital, China
Executive brief
Investment-Ready Snapshot
Multicenter, Single-Arm Exploratory Phase I Clinical Study on the Safety and Efficacy of Fully Human BAFF-R Chimeric Antigen Receptor T-Cell Injection in Participants With Relapsed/Refractory BAFF-R-Positive B-Cell Lymphoma is a PHASE1 clinical asset sponsored by Institute of Hematology & Blood Diseases Hospital, China in DLBCL, CLL, FL, MCL, WM, MZL. SEO and diligence focus: BAFF-R CAR-T, endpoint relevance, enrollment feasibility, competitive positioning, readout timing and IP durability.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT07259070
Indication
DLBCL
Modality
cell therapy
Target
BAFF-R CAR-T
Intervention
BAFF-R CAR-T
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.