Autopsy report · NCT03686033
A Study to Evaluate the Pharmacodynamic Activity of E2082 in Adult Participants With Photosensitive Epilepsy
Cause of deathSafety
“Safety Review”
Life of this trial
- Registered 1 month before it started.
- Ran for about 8 months before it stopped.
- 8 participants enrolled.
- Results were posted on the registry 1 year 3 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- Eisai Inc.
- Sponsor type
- Industry
- Conditions
- Photosensitive Epilepsy
- Interventions
- Placebo; E2082
- Participants
- 8
- Sites
- 5
- Countries
- United States
Trials that died the same way
- A Phase I Trial of a LTK63 Adjuvated Tuberculosis Nasal Subunit Vaccine (Ag85B-ESAT6)
“Safety Issues” - Safety and Tolerability of Tozadenant as Adjunctive Therapy in Levodopa-Treated Patients With Parkinson's Disease.
“New Safety Information” - Safety and Pharmacokinetics (PK) of a Polyurethane Tenofovir Disoproxil Fumarate (TDF) Vaginal Ring (TDF IVR-002)
“Safety-related” - Timing for Removal of Chest Tubes in Adult Cardiac Surgery
“Safety interim analysis” - AGN-242428 in the Treatment of Plaque Psoriasis
“safety reason”
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.