Autopsy report · NCT02028312
A Phase IV, Randomized, Parallel Group, Investigator-Masked Evaluation of the Effect of Loteprednol Etabonate Ophthalmic Gel 0.5% on the Initiation of Dry Eye Treatment With Restasis®
Cause of deathFunding or business
“Per Sponsor”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Phase 4
- Sponsor
- Edward Holland, MD
- Sponsor type
- University, hospital or other
- Conditions
- Dry Eye Disease
- Interventions
- Loteprednol etabonate; Artificial Tears; Restasis
- Participants
- 0
- Sites
- 1
- Countries
- United States
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“Sponsor related” - An Open-Label Extension of XPro1595 in Patients With Alzheimer's Disease
“Sponsor resource allocation” - Research Study to Compare Semaglutide Tablets With Empagliflozin Tablets Taken Once Daily in People With Type 2 Diabetes and Obesity
“Sponsor decision”
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.