Phase I/Ib Clinical Trial of Autologous CD22 Chimeric Antigen Receptor (CAR) T Cells Following Commercial CD19 CAR T Cells in Children and Young Adults With Recurrent or Refractory B Cell Malignancies
This clinical trial, sponsored by Stanford University, investigates the safety and feasibility of autologous CD22 CAR T cell therapy administered after commercial CD19 CAR T cell therapy (Tisagenlecleucel) in pediatric and young adult patients with relapsed or refractory B-cell malignancies. The trial targets a niche but critical segment of the oncology market, particularly in pediatric leukemia, where there is a significant unmet need for effective therapies following initial CAR T cell treatments. Given the increasing prevalence of CAR T therapies and the potential for combination strategies, this trial could position Stanford as a leader in advancing CAR T cell therapies, potentially enhancing its competitive edge against other institutions and biopharmaceutical companies in the CAR T space. The successful outcomes could lead to expanded indications for CAR T therapies and increased market share for related products.
Indication: Leukemia
Modality: small molecule
Target: CD22 Chimeric Antigen Receptor (CAR) T Cells
Sponsor: Stanford University
Source URL: ClinicalTrials.gov
Source updated: Detailed source ingestion pending
Ingested: Jun 25, 2026
Model: trialsignal-ai-v1
Validation: validated
Matched by target_normalized: CD22 Chimeric Antigen Receptor (CAR) T Cells
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Condition raw: Leukemia, Acute Lymphoblastic Leukemia
Condition normalized: Leukemia, Acute Lymphoblastic Leukemia
Modality raw: small molecule
Modality normalized: small molecule
Target raw: CD22 Chimeric Antigen Receptor (CAR) T Cells
Target normalized: CD22 Chimeric Antigen Receptor (CAR) T Cells