CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 20 enrolled
Drug / intervention
GSK2256294 +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.

Search/NCT03318783
NCT03318783Phase 2Completed

Subarachnoid Hemorrhage and Soluble Epoxide Hydrolase Inhibition Trial

Oregon Health and Science University·interventional·Posted Oct 24, 2017·Updated Jan 22, 2021

In Brief

A Phase 2 clinical trial evaluating GSK2256294 and Placebo for Subarachnoid Hemorrhage, Aneurysmal and 3 related conditions. Completed, enrolled 20 participants across 1 site.

Detailed Summary

Soluble epoxide hydrolase (sEH) is the metabolizing enzyme of epoxyeicosatrienoic acids (EETs), which may play a role in reducing neuroinflammation and regulating cerebral blood flow after subarachnoid hemorrhage (SAH). Hypotheses: Pharmacologic inhibition of the sEH enzyme is safe and will result in increased EETs availability in the blood and cerebrospinal fluid. This study is a double-blind, placebo-controlled, phase 1b randomized trial to evaluate the safety and efficacy of GSK2256294, a novel soluble epoxide hydrolase inhibitor in patients with aneurysmal SAH.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2CompletedFinished
201820192020202120222023202420252026
First PostedOct 24, 2017
Enrollment StartMay 2, 2018
Primary CompletionApr 3, 2019
Study CompletionJan 9, 2020
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 8.7 years ago

Interventions

GSK2256294drug

GSK2256294 will be administered in a single dose once daily enteral for a duration of 10 days.

Placebodrug

Placebo will be administered in a single dose once daily enteral for a duration of 10 days.