At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 51 enrolled
Drug / intervention
Tildrakizumabdrug
Likely dose
Tildrakizumab 100 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Phase II Trial of Tildrakizumab for Prevention of Acute Graft-Versus-Host Disease
In Brief
A Phase 2 clinical trial evaluating Tildrakizumab for Hematologic Malignancies. Completed, enrolled 51 participants across 1 site.
Detailed Summary
This is a phase 2 open-label trial designed to evaluate the efficacy of tildrakizumab in improving graft-versus-host disease (GVHD)-free relapse-free survival after myeloablative allogeneic hematopoietic cell transplantation (alloHCT) for hematologic malignancy.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHematologic Malignancies
CountriesUnited States
Collaborators--
Timeline
Phase 2CompletedFinished
2020202120222023202420252026
First PostedOct 2019
Enrollment StartMar 2020
Primary CompletionJun 2024
Study CompletionJun 2024
TodayJul 2026
First PostedOct 2, 2019
Enrollment StartMar 1, 2020
Primary CompletionJun 1, 2024
Study CompletionJun 17, 2024
TodayJul 2, 2026
Enrollment to primary: 4.3 yearsPosted 6.8 years ago
Interventions
Tildrakizumabdrug
100 mg will be injected subcutaneously on Day -1, Day 28 ± 3, Day 112 ± 7, Day 196 ± 14, and Day 280 ± 14.