Chimeric Antigen Receptor (CAR)-T Cell Therapy for Patients With Hematologic Malignancies
This Phase 2 clinical trial, sponsored by the Masonic Cancer Center at the University of Minnesota, evaluates FDA-approved CAR-T therapies (Kymriah, Yescarta, and Tecartus) for treating hematologic malignancies, specifically B-cell acute lymphoblastic leukemia (ALL) and diffuse large B-cell lymphoma (DLBCL). The trial's focus on multiple CAR-T products positions it strategically within a competitive landscape dominated by established therapies. The outcomes may influence market dynamics, particularly in the pediatric and adult oncology segments, where CAR-T therapies are gaining traction. The trial's results could enhance the commercial viability of these therapies, especially in refractory cases, and provide critical data for regulatory submissions and market access strategies.
Indication: Acute Lymphoblastic Leukemia
Modality: gene therapy
Target: CD19-directed genetically modified autologous T cell immunotherapy
Sponsor: Masonic Cancer Center, University of Minnesota
Source URL: ClinicalTrials.gov
Source updated: Detailed source ingestion pending
Ingested: Jul 22, 2026
Model: trialsignal-ai-v1
Validation: validated
Matched by target_normalized: CD19-directed genetically modified autologous T cell immunotherapy
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Condition raw: Acute Lymphoblastic Leukemia, Large B-cell Lymphoma
Condition normalized: Acute Lymphoblastic Leukemia, Large B-cell Lymphoma
Modality raw: gene therapy
Modality normalized: gene therapy
Target raw: CD19-directed genetically modified autologous T cell immunotherapy
Target normalized: CD19-directed genetically modified autologous T cell immunotherapy