Phase II Clinical Study on the Safety and Efficacy of Autotransfusion Agents Targeting CD19 Chimeric Antigen Receptor T Lymphocytes (BIC-19GG, BIC-2019,BIC-2219)in the Treatment of CD19-positive Children With Relapsed/Refractory B-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
The Phase II study evaluates the safety and efficacy of three autotransfusion agents (BIC-19GG, BIC-2019, BIC-2219) targeting CD19 in pediatric patients with relapsed/refractory B-cell acute lymphoblastic leukemia (ALL) and lymphoblastic lymphoma. Given the high unmet medical need in this patient population, successful outcomes could position these agents favorably in the competitive landscape of CAR T-cell therapies, which have shown promise but also face challenges such as high costs and adverse effects. The market for CAR T-cell therapies is expanding, with significant investment and interest from major biopharmaceutical companies, indicating potential for lucrative partnerships or acquisitions if the trial demonstrates positive results.
Indication: B Lymphocytic Leukemia
Modality: medical device
Target: CD19 Chimeric Antigen Receptor T Lymphocytes
Sponsor: Zhu Xiaofan
Source URL: ClinicalTrials.gov
Source updated: Detailed source ingestion pending
Ingested: Jul 18, 2026
Model: trialsignal-ai-v1
Validation: validated
Matched by target_normalized: CD19 Chimeric Antigen Receptor T Lymphocytes
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Condition raw: B Lymphocytic Leukemia, B Lymphoblastic Lymphoma
Condition normalized: B Lymphocytic Leukemia, B Lymphoblastic Lymphoma
Modality raw: medical device
Modality normalized: medical device
Target raw: CD19 Chimeric Antigen Receptor T Lymphocytes
Target normalized: CD19 Chimeric Antigen Receptor T Lymphocytes