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NCT05970224CompletedPhase 2

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

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

Source: ClinicalTrials.gov · Last updated 23 Jul 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
23 (actual)
First submitted
24 Jul 2023
Start date
17 Nov 2023
Primary completion date
20 Mar 2026
Lead sponsor
Bioxodes S.A.
Diseases
Stroke
NCT number
NCT05970224
EU CT number
2022-500491-53-00

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 23
  • From 17 Nov 2023 to the primary completion date, 20 Mar 2026
  • 8 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Planned neurosurgical hematoma evacuation or other urgent surgical intervention (i.e., surgical relief of increased intracranial pressure) on initial presentation.
  • Use of immunosuppressive or immune-modulating therapy at admission (e.g., steroids, methotrexate, monoclonal antibodies, etc).

Other illness

  • History of personal or familial bleeding disorders; including prolonged or unusual bleeding.
  • Patients with intraventricular haemorrhage (IVH) having a Graeb score of \>3 on initial presentation. Patients must not have blood in the 4th ventricle and may only have blood in the 3rd ventricle in the absence of ventricular expansion. Trace or mild haemorrhage in either or both lateral ventricles is permitted. Patients with hydrocephalus determined radiologically on initial presentation are excluded regardless of Graeb score.
  • Patients with active systemic bacterial, viral or fungal infections.

Lab values

  • Severe renal impairment (eGFR \< 30 mL/min/1.73 m2).

Other

  • Known deficiency in factor XII (FXII) or haemophilia type A (FVII) or type B (FIX) or type C (FXI).
  • Infratentorial (midbrain, pons, medulla, or cerebellum) ICH.
  • Secondary ICH due to aneurysm, brain tumour, arteriovenous malformation, thrombocytopenia, coagulopathy, acute sepsis, traumatic brain injury (TBI), or disseminated intravascular coagulation (DIC).
  • Anticoagulation reversal treatment.
  • Women of childbearing potential.
  • Have a body weight \> 120 kg at screening.

Who the study is looking for

  • Male or female patients aged ≥ 18 years.
  • Written informed consent obtained before any study assessment. If the patient is not able to give the informed consent personally, consent by a legal representative as defined by local law and regulation is acceptable.
  • First-ever, spontaneous, supratentorial intracerebral haemorrhage in cerebral cortex or deep brain structures (putamen, thalamus, caudate, and associated deep white matter tracts) with a volume ≥ 5 mL and ≤ 60 mL determined by non-contrast CT scan.
  • Patients with Glasgow Coma Scale (GCS) best motor score no less than 5.
  • Modified Rankin Scale (mRS) score 0-2 prior to ICH symptom onset.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (8)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
AZ Sint Jan
Coordinator of this site? Confirm its status
BrugesBelgiumUnknown status
UZ Brussel
Coordinator of this site? Confirm its status
BrusselsBelgiumUnknown status
UCL St-Luc
Coordinator of this site? Confirm its status
BrusselsBelgiumUnknown status
UZ Gent
Coordinator of this site? Confirm its status
GhentBelgiumUnknown status
UZ Leuven
Coordinator of this site? Confirm its status
LeuvenBelgiumUnknown status
Clinique CHC MontLégia
Coordinator of this site? Confirm its status
LiègeBelgiumUnknown status
CHU Ambroise Paré
Coordinator of this site? Confirm its status
MonsBelgiumUnknown status
AZ Damiaan
Coordinator of this site? Confirm its status
OstendBelgiumUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.