38
Participants
Start Date
August 28, 2017
Primary Completion Date
September 30, 2019
Study Completion Date
January 25, 2020
CN-105
Patients with supratentorial intracerebral hemorrhage (ICH) will be evaluated for eligibility within 12 hours of symptom onset. Eligible participants will receive CN-105 administered intravenously (IV) for a 30 -minute infusion every 6 hours for up to a maximum of 3 days (13 doses) or until discharge (if earlier than 3 days)
University of Virginia Health Systems, Charlottesville
Wake Forest Baptist Health, Winston-Salem
Duke University Health System, Durham
Medical University of South Carolina, Charleston
A.B. Chandler Medical Center-University of Kentucky, Lexington
Lead Sponsor
Collaborators (2)
Duke Clinical Research Institute
OTHER
PharPoint Research, Inc.
INDUSTRY
AegisCN LLC
INDUSTRY