Telemedicine for Early Detection of Cytokine Release Syndrome and Neurotoxicity Following CAR-T Infusion on an Outpatient Basis
The trial aimed to evaluate the feasibility of telemedicine in monitoring patients undergoing CAR-T therapy for relapsed or refractory large B-cell lymphoma. Given the increasing adoption of telehealth solutions, especially post-COVID-19, this approach could enhance patient management and reduce healthcare costs. However, the trial was withdrawn, indicating potential challenges in execution or strategic alignment. The market for CAR-T therapies is expanding, with significant competition from established players and emerging biotech firms. Companies should consider the implications of telemedicine integration in their CAR-T programs to improve patient outcomes and operational efficiencies.
Indication: Large B-cell Lymphoma
Modality: cell therapy
Target: Cytokine Release Syndrome (CRS) and Neurotoxicity assessment in CAR-T therapy patients.
Sponsor: Wake Forest University Health Sciences
Source URL: ClinicalTrials.gov
Source updated: Detailed source ingestion pending
Ingested: Jul 22, 2026
Model: trialsignal-ai-v1
Validation: validated
Matched by target_normalized: Cytokine Release Syndrome (CRS) and Neurotoxicity assessment in CAR-T therapy patients.
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Condition raw: Large B-cell Lymphoma, Diffuse Large B Cell Lymphoma, Primary Mediastinal Large B Cell Lymphoma, High-grade B-cell Lymphoma, Follicular Lymphoma
Condition normalized: Large B-cell Lymphoma, Diffuse Large B Cell Lymphoma, Primary Mediastinal Large B Cell Lymphoma, High-grade B-cell Lymphoma, Follicular Lymphoma
Modality raw: cell therapy
Modality normalized: cell therapy
Target raw: Cytokine Release Syndrome (CRS) and Neurotoxicity assessment in CAR-T therapy patients.
Target normalized: Cytokine Release Syndrome (CRS) and Neurotoxicity assessment in CAR-T therapy patients.