EichorEICHOR
Study identifier: NCT05970224 Synced from ClinicalTrials.gov · August 02, 2026
● Completed

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

Condition: Intracerebral Hemorrhage  ·  Sponsor: Bioxodes S.A.

PhasePhase 2
Planned participants23
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (8)

UZ GentGhent, East Flanders, Belgium
UZ LeuvenLeuven, Flemish Brabant, Belgium
CHU Ambroise ParéMons, Hainaut, Belgium
AZ Sint-JanBruges, West Flanders, Belgium
AZ DamiaanOstend, West Flanders, Belgium
UCL St LucBrussels, Belgium
UZ BrusselBrussels, Belgium
Clinique CHC MontLégiaLiège, Belgium

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