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
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.
Indication: CLL/SLL
Modality: cell therapy
Target: CD19 (Chimeric Antigen Receptor T Cell Therapy) and engineered IL-2 receptor (hoRb)
Sponsor: Synthekine
Source URL: ClinicalTrials.gov
Source updated: Detailed source ingestion pending
Ingested: Jul 15, 2026
Model: trialsignal-ai-v1
Validation: validated
Matched by target_normalized: CD19 (Chimeric Antigen Receptor T Cell Therapy) and engineered IL-2 receptor (hoRb)
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Condition raw: CLL/SLL, NHL, Mantle Cell Lymphoma, Follicular Lymphoma, Large B-cell Lymphoma, Indolent B-Cell Non-Hodgkin Lymphoma, Diffuse Large B Cell Lymphoma
Condition normalized: CLL/SLL, NHL, Mantle Cell Lymphoma, Follicular Lymphoma, Large B-cell Lymphoma, Indolent B-Cell Non-Hodgkin Lymphoma, Diffuse Large B Cell Lymphoma
Modality raw: cell therapy
Modality normalized: cell therapy
Target raw: CD19 (Chimeric Antigen Receptor T Cell Therapy) and engineered IL-2 receptor (hoRb)
Target normalized: CD19 (Chimeric Antigen Receptor T Cell Therapy) and engineered IL-2 receptor (hoRb)