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Specifying the Anti-inflammatory Effects of Ziltivekimab (SPIDER)

Key facts

Where
Amsterdam, HollandiaSee the site
Phase
2/3. fázis

Where in Hollandia

  • Amsterdam UMC StichtingAmsterdam, HollandiaNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Stichting Amsterdam UMC
Trial code
EU 2024-515893-29-01
Record updated
2024. november 19.
Original description
The objective of this study is to research whether ziltivekimab therapy for 20 weeks reduces arterial wall inflammation, as assessed by state-of-the-art imaging modalities, and reduces systemic inflammatory tone, as assessed by in depth phenotyping of circulating monocytes, inflammatory biomarkers and proteomics.Read full original descriptionShow less

Specifying the anti-inflammatory effects of ziltivekimab with diverse imaging modalities and in-depth cellular phenotyping (SPIDER)

The objective of this study is to research whether ziltivekimab therapy for 20 weeks reduces arterial wall inflammation, as assessed by state-of-the-art imaging modalities, and reduces systemic inflammatory tone, as assessed by in depth phenotyping of circulating monocytes, inflammatory biomarkers and proteomics.

Inclusion: Age 50 years and older; Multi-vessel coronary artery disease (defined as CAD-RADS ≥2 and/or PAV/NCPV stage ≥2); Serum hsCRP level ≥2 mg/L.

Exclusion: Chronic or recent (<1 month) (serious) infections and/or clinical signs of acute (serious) infection; History of severe auto-immune diseases, or other (severe) (recurrent or chronic) inflammatory disorders; Untreated latent tuberculosis, active hepatitis B (positive HBsAg and/or positive anti-HBc with detectable HBV DNA) or C, human immunodeficiency virus (HIV) not on stable antiretroviral regimen; Coronary stents in situ.

EU CTIS 2024-515893-29-01