At a glance
ClinicalIndex Comparison RecordPhase 2Recruiting· 24 target
Drug / intervention
Allogeneic Bone-Marrow Derived Mesenchymal Stromal Cells Secretome +1 moredrug
Likely dose
Not stated in 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.
NCT06919081Phase 2RecruitingMonitorUpdated 5mo ago · Completion was 3mo agoSlow Enrollment
Monitor
Phase II Study of the Efficacy of Topical Mesenchymal Stromal Cell Secretome for Ocular Surface Disease
In Brief
A Phase 2 clinical trial evaluating Allogeneic Bone-Marrow Derived Mesenchymal Stromal Cells Secretome and Vehicle Control for Persistent Corneal Epithelial Defect and Corneal Epithelial Disorders. Currently recruiting, targeting 24 participants across 1 site.
Signals
Enrolling slower than its timeline implies
Detailed Summary
In this phase II randomized double-masked clinical trials, subjects with non-resolving corneal epithelial disease/defect (i.e., refractory to standard treatments for at least two weeks) will receive 8 weeks treatment of topical mesenchymal stem cell secretome or vehicle, with continued follow-up for up to Day 70.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Timeline
Phase 2RecruitingOverdue
2026
First PostedApr 2025
Enrollment StartAug 2025
Primary CompletionMar 2026
Study CompletionJun 2026
TodayJul 2026
First PostedApr 9, 2025
Enrollment StartAug 1, 2025
Primary CompletionMar 15, 2026
Study CompletionJun 15, 2026
TodayJul 1, 2026
Enrollment to primary: 7 monthsPosted 1.2 years ago
Interventions
Allogeneic Bone-Marrow Derived Mesenchymal Stromal Cells Secretomedrug
Eye Drops
Vehicle Controlother
Eye Drops