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COMPLETED
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

2026-06-22

Last Updated

2026-07-23

Healthy Volunteers

No

Interventions

DRUG

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