A Proof of Concept Study to Evaluate CN-105 in ICH Patients

PHASE2CompletedINTERVENTIONAL
Enrollment

38

Participants

Timeline

Start Date

August 28, 2017

Primary Completion Date

September 30, 2019

Study Completion Date

January 25, 2020

Conditions
Intracerebral Hemorrhage
Interventions
DRUG

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)

Trial Locations (5)

22908

University of Virginia Health Systems, Charlottesville

27103

Wake Forest Baptist Health, Winston-Salem

27709

Duke University Health System, Durham

29425

Medical University of South Carolina, Charleston

40536

A.B. Chandler Medical Center-University of Kentucky, Lexington

All Listed Sponsors
collaborator

Duke Clinical Research Institute

OTHER

collaborator

PharPoint Research, Inc.

INDUSTRY

lead

AegisCN LLC

INDUSTRY

NCT03168581 - A Proof of Concept Study to Evaluate CN-105 in ICH Patients | Biotech Hunter | Biotech Hunter