Autopsy report · NCT06411132
Study to Evaluate Corneal Neurosensory Abnormalities in Patients With Sjögren's Dry Eye
Cause of deathOther
“The analyses presented are based on a database lock date of 05 March 2025.The study was prematurely interrupted by Dompé following a review of the database, which determined that an acceptable no. of patients was reached to meet the trial objectives.”
Life of this trial
- Ran for about 8 months before it stopped.
- 103 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Sponsor
- Dompé Farmaceutici S.p.A
- Sponsor type
- Industry
- Conditions
- Sjögren Syndrome; Dry Eye
- Interventions
- observational study
- Participants
- 103
- Sites
- 15
- Countries
- United States
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“The study was interrupted early and terminated when only 26 out of 80 patients were enrolled due to new clinical study results indicating that the current study would not be informative.” - AZD1222 Vaccine for the Prevention of COVID-19
“The study was put on hold in September 2020 due to a safety concern in another trial but never restarted. In the meantime our clinical development program now includes a similar study with a different design, which we prefer to complete now.” - A Study of Obinutuzumab in Combination With CHOP Chemotherapy Versus Rituximab With CHOP in Participants With CD20-Positive Diffuse Large B-Cell Lymphoma (GOYA)
“The study was closed by the Sponsor according to the protocol-specified minimum post-treatment follow-up period of 3 years.” - Inotropic Treatment With Levosimendan (SimdaxR)in Heart Surgery
“The study was stopped due to difficulties in including patients” - Study of the Safety and Effectiveness of Two Doses of Investigational Study Drug EVP-6124 in Subjects With Alzheimer's Disease
“Study has been suspended due to clinical hold.”
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.