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A Study to Evaluate the Safety, Tolerability and the Effects of Ixodes Ricinus-Contact Phase Inhibitor (Ir-CPI) in Adult Patients With Spontaneous Intracerebral Haemorrhage
Sponsor: Bioxodes S.A.
Summary
The purpose of the study is to provide a first assessment of safety, tolerability and efficacy of Ir-CPI, administered on top of standard-of-care, on secondary brain injury in patients with spontaneous intracerebral haemorrhage.
Official title: A Phase IIa, Randomized, Open-label, Proof-of-Concept Study to Evaluate Safety, Tolerability and Efficacy of Ir-CPI in Patients With Spontaneous Intracerebral Haemorrhage
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
23
Start Date
2023-11-17
Completion Date
2027-07
Last Updated
2026-03-27
Healthy Volunteers
No
Conditions
Interventions
Ir-CPI
Participants receive a single intravenous dose of Ir-CPI during 48 hours
Locations (10)
HUB Erasme
Brussels, Brussels Capital, Belgium
UCL St Luc
Brussels, Brussels Capital, Belgium
UZ Brussel
Brussels, Brussels Capital, Belgium
UZ Gent
Ghent, East Flanders, Belgium
UZ Leuven
Leuven, Flemish Brabant, Belgium
CHU Ambroise Paré
Mons, Hainaut, Belgium
AZ Sint-Jan
Bruges, West Flanders, Belgium
AZ Groeninge
Kortrijk, West Flanders, Belgium
AZ Damiaan
Ostend, West Flanders, Belgium
Clinique CHC MontLégia
Liège, Belgium