drugset / Trial / NCT00940095

Clazosentan in Aneurysmal Subarachnoid Hemorrhage

NCT00940095 ↗

Phase 3 Terminated 577 enrolled Idorsia Pharmaceuticals Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The aim of this study is to demonstrate that clazosentan, administered as a continuous intravenous infusion at either 5 mg/h or 15 mg/h until Day 14 post aneurysmal subarachnoid hemorrhage (aSAH), reduces the incidence of cerebral vasospasm-related morbidity and all-cause mortality within 6 weeks post-aSAH treated by endovascular coiling. The primary endpoint of the study is the occurrence of cerebral vasospasm-related morbidity, and mortality of all-causes within 6 weeks post-aSAH, defined by at least one of the following: 1. Death (all causes). 2. New cerebral infarct(s) due to cerebral vasospasm as either the primary or relevant contributing cause, or not adjudicated to be entirely due to causes other than vasospasm. 3. Delayed ischemic neurological deficit (DIND) due to cerebral vasospasm as either the primary or relevant contributing cause, or not adjudicated to be entirely due to causes other than vasospasm. 4. Administration of a valid rescue therapy in the presence of confirmed cerebral vasospasm on angiography (DSA or CTA). An independent Critical Events Committee (CEC) will adjudicate whether or not patients meet the primary endpoint and its individual morbidity components.

Timeline

Start
2009-07-01
Primary completion
2010-10-01
Completion
2011-01-01

Outcome

Met primary endpoint

Stopped: “Lack of efficacy data from the Phase 3 clinical study (AC-054-301; CONSCIOUS-2)”

paper Clazosentan 15 mg/h significantly reduced postaSAH vasospasm-related morbidity/all-cause mortality PMID 22403047 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Clazosentan Small molecule 5 mg Intravenous
Subject Clazosentan Small molecule 15 mg Intravenous