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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
2026-06-22
Last Updated
2026-07-23
Healthy Volunteers
No
Conditions
Interventions
Ir-CPI
Participants receive a single intravenous dose of Ir-CPI during 48 hours
Locations (8)
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 Damiaan
Ostend, West Flanders, Belgium
UCL St Luc
Brussels, Belgium
UZ Brussel
Brussels, Belgium
Clinique CHC MontLégia
Liège, Belgium