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A Phase 1 Multicenter Study Evaluating the Safety and Tolerability of KTE-X19 in Adult Subjects With Relapsed/Refractory Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 24, 2026
Report code
NCT03624036-Jun 24, 2026
NCT ID
NCT03624036
Status
TERMINATED
Phase
Phase 1
Sponsor
Kite, A Gilead Company
Executive brief
Investment-Ready Snapshot
Brexucabtagene autoleucel (KTE-X19) is a CAR T-cell therapy targeting CD19, specifically developed for adult patients with relapsed/refractory chronic lymphocytic leukemia (r/r CLL) and small lymphocytic lymphoma (r/r SLL). The therapy aims to address a significant unmet need in a patient population that has limited treatment options after multiple lines of therapy, particularly those who have previously received Bruton's tyrosine kinase (BTK) inhibitors. The termination of the development program may indicate challenges in achieving desired efficacy or safety profiles, which could impact Kite's competitive positioning in the CAR T-cell therapy market. The ongoing follow-up study (NCT05041309) may yield long-term safety and efficacy data that could influence future strategic decisions or partnerships.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03624036
Indication
Relapsed/Refractory Chronic Lymphocytic Leukemia and Relapsed/Refractory Small Lymphocytic Lymphoma
Modality
cell therapy
Target
CD19 (Cluster of Differentiation 19)
Intervention
brexucabtagene autoleucel, Fludarabine, 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.