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

StatusActive, Not Recruiting
PhasePhase 1/2
Started2018-01-24
View on ClinicalTrials.gov ↗
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.

Amendment history 4 changes detected by DataLookout

2026-08-15
notable
Enrollment closed, study ongoing
2026-08-15
critical
Enrollment reduced: 36 → 2 participants
2026-08-15
critical
Primary completion pushed: 2025-07 → 2026-11-05
2026-08-15
minor
Completion pushed: 2025-11 → 2026-12-15
Trial Details
NCT Number NCT03594981
Lead Sponsor Catherine Bollard
Collaborators: M.D. Anderson Cancer Center
Conditions Viral Infection
Enrollment 2 participants
Start Date 2018-01-24
Primary Completion 2026-11-05 (estimated)
Study Completion 2026-12-15 (estimated)
Updated on ClinicalTrials.gov 2026-08-14