drugset / Trial / NCT03594981

Adoptive Cord Blood Immunotherapy for EBV, CMV, BKV and Adenovirus Reactivation/Infection or Prophylaxis

NCT03594981 ↗

Phase 1/2 Recruiting 36 enrolled Catherine Bollard M.D. Anderson Cancer Center · collab
NaSingle-groupOpen-labelTreatment

Summary

This Phase I-II dose-finding trial to determine the optimal dose of intravenous (IV) injection dose of donor-derived cytotoxic T lymphocytes (CTLs) specific for CMV, EBV, BKV and Adenovirus. A maximum of 36 patients will be treated in up to 18 cohorts each of size 2, with the first cohort treated at the lowest dose level 1, all successive doses chosen by the EffTox method, and no untried dose level skipped when escalating. The scientific goal of the trial is to determine an optimal IV-CTL cell dose level among the three doses 1.0x107cells/m2, 2 x107cells/m2 and 5x107cells/m2., hereafter dose levels 1, 2, 3. Dose-finding will be done using the sequentially adaptive EffTox trade-off-based design of Thall et al.

Timeline

Start
2018-01-24
Primary completion
2025-07
Completion
2025-11

Drugs

EvaluationDrugModalityDoseRoute
Subject CMV/AdV /EBV/BKV specific T cells Cell therapy 1e+07 unknown Intravenous
Subject CMV/AdV /EBV/BKV specific T cells Cell therapy 2e+07 unknown Intravenous
Subject CMV/AdV /EBV/BKV specific T cells Cell therapy 5e+07 unknown Intravenous