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ACTIVE NOT RECRUITING
NCT05970224
PHASE2

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.

View on ClinicalTrials.gov

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

Interventions

DRUG

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