Autopsy report · NCT02309736
OTX-14-002: Device Exposure Registry
Cause of deathRegulatory or ethics
“On going discussions with FDA”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Sponsor
- Ocular Therapeutix, Inc.
- Sponsor type
- Industry
- Conditions
- Endophthalmitis
- Interventions
- ReSure Sealant
- Participants
- 0
Trials that died the same way
- MAS-1 Adjuvanted Compared to Unadjuvanted Influenza Vaccines in the Elderly
“FDA hold on the project” - Perceval S Aortic Heart Valve Study- North America
“FDA approval” - Safety and Efficacy of Bevacizumab in Combination With NaviFUS System for the Treatment of Recurrent Glioblastoma Multiforme (rGBM)
“FDA reviewing” - Pilot Study Of Anti-Programmed Death Ligand-1 (Anti-PD-L1, Atezolizumab) In Asymptomatic Myeloma
“Based on FDA requirements” - Safety of SP-420 in the Treatment of Transfusional Iron Overload
“Study is on hold by FDA in the US.”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.