TrialSignal
Clinical trial intelligence report
A Phase Ia Study of Tri-specific CAR19.20.22 Chimeric Antigen Receptor (CAR) T-cells for Patients With Relapsed/Refractory B-Cell Lymphomas
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT07168486-Jul 28, 2026
NCT ID
NCT07168486
Status
ENROLLING_BY_INVITATION
Phase
Phase 1a
Sponsor
University of Maryland, Baltimore
Executive brief
Investment-Ready Snapshot
The Phase 1a trial of CAR19.20.22 CAR T-cells, sponsored by the University of Maryland, aims to address the unmet medical need for patients with relapsed/refractory B-cell lymphomas, particularly those expressing multiple target antigens. The market for CAR T-cell therapies is expanding, with significant competition from existing therapies such as Kymriah and Yescarta. The success of this trial could position the University of Maryland as a key player in the CAR T-cell landscape, particularly if the asset demonstrates superior efficacy and safety profiles. Given the increasing demand for innovative therapies in oncology, successful outcomes may lead to strategic partnerships or licensing opportunities with larger biopharmaceutical companies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT07168486
Indication
B-Cell Lymphoma
Modality
protein therapy
Target
Tri-specific CAR19.20.22 Chimeric Antigen Receptor targeting CD19, CD20, and CD22 antigens on B-cell malignancies.
Intervention
CD19.20.22 CAR T cells, Fludarabine and Cyclophosphamide
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.