TrialSignal
Clinical trial intelligence report
A Phase 1 Study to Evaluate the Safety and Tolerability of a Combination Autologous CD19 CAR T Cell Therapy (SYNCAR-001 + STK-009) in Subjects With Relapsed or Refractory CD19+ Hematologic Malignancies
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT05665062-Jul 28, 2026
NCT ID
NCT05665062
Status
ACTIVE_NOT_RECRUITING
Phase
Phase 1
Sponsor
Synthekine
Executive brief
Investment-Ready Snapshot
Synthekine's SYNCAR-001 + STK-009 is positioned in the competitive landscape of CAR T-cell therapies targeting CD19+ hematologic malignancies, specifically Chronic Lymphocytic Lymphoma (CLL) and Non-Hodgkin's Lymphoma (NHL). The combination therapy aims to enhance efficacy and safety profiles compared to existing CD19-targeted therapies. The market for CAR T therapies is rapidly expanding, with significant demand for innovative treatments in relapsed or refractory cases. The trial's focus on safety and tolerability will be critical for future regulatory approvals and market entry. Given the estimated completion date in 2041, Synthekine may face competitive pressures from other emerging therapies and established players in the CAR T space, necessitating robust clinical data to support differentiation.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05665062
Indication
CLL/SLL
Modality
cell therapy
Target
CD19 (Chimeric Antigen Receptor T Cell Therapy) and engineered IL-2 receptor (hoRb)
Intervention
SYNCAR-001, STK-009, Cyclophosphamide, Fludarabine
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.