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Study identifier: NCT07685457 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Evaluation of Safety and Efficacy of Virus Specific T-Cell Administration in Pediatric Patients With Systemic Viral Infection Following Allogeneic Hematopoietic Stem Cell Transplantation.

Condition: BKV Infection · CMV Infection · EBV Infection  ·  Sponsor: LucasBio

PhaseNA
Planned participants6
Who can joinAll sexes, 1 Year to 25 Years
Healthy volunteersNo

About this study

The goal of this prospective clinical study is to evaluate the safety and efficacy of Multi-Virus Specific T cells (LB-DTK-MV) in pediatric patients with systemic viral infection, including CMV, EBV, and BKV, after allogeneic hematopoietic stem cell transplantation (allo-HSCT). The main questions it aims to answer are: * What is the maximum tolerated dose of LB-DTK-MV based on dose-limiting toxicity? * What treatment emergent adverse events occur within 14 days after the second infusion? * Is there a clinically significant reduction in CMV, EBV, and BKV viral loads within 14 days following the second infusion? * Is there a clinically significant improvement in clinical symptoms within 14 days following the second infusion? Participants will: * Receive a single intravenous infusion of LB-DTK-MV during the baseline visit (low dose: 1x10\^7/m\^2; high dose: 2x10\^7/m\^2). * Receive the second infusion of LB-DTK-MV intravenously at the same dose 14 days after the first infusion. * Attend weekly follow-up visits at the clinic for 6 months after the first infusion.

This description comes directly from the study's public registry record.

Talk to the study team

Nayoun Kim, Ph.D.  ·  +82 1040222340  ·  nkim@lucasbio.com

Always discuss trial participation with your own doctor first.

Locations (1)

The Catholic University of Korea Seoul St.Mary's HospitalSeoul, South KoreaRecruiting

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Source record: clinicaltrials.gov/study/NCT07685457