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NCT07830719RecruitingPhase 2

A clinical trial to learn more about the effects of YMI024 in people with coronary artery disease

A Phase 2b, multicenter, randomized, double-blind, placebo-controlled, parallel-group, dose-finding study of YMI024 to assess efficacy in reducing inflammatory markers, safety, and tolerability in adults with stable coronary artery disease and elevated hsCRP

Source: EU CTIS (euclinicaltrials.eu) · Last updated 5 Aug 2026

Brief summary (registry, in English)

To evaluate the dose-response relationship of YMI024 compared with placebo in reducing inflammatory markers in adults with stable CAD and elevated hsCRP ≥2 mg/L

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
43 (estimated)
First submitted
16 Jun 2026
Start date
29 Sept 2026
Lead sponsor
Novartis Pharma AG
EU CT number
2026-525974-21-00

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 43
  • 14 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study, not your situation.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participants who have certain heart problems, like a heart attack within 30 days before entering the trial

Other illness

  • Participants who have undergone open heart surgery in the past 6 months
  • Participants who have an autoimmune disease like rheumatoid arthritis or Crohn’s disease or ulcerative colitis and are taking certain therapies to treat, or if they have certain chronic infections such as hepatitis B or C

Who the study is looking for

  • Signed informed consent must be obtained prior to any study specific procedures, and participant able to understand and comply with study requirements.
  • Male and female participants aged between 18-80 years (inclusive) at Screening.
  • Confirmed diagnosis of CAD
  • Participants have CRP levels more than ≥2 mg/L, which is a sign of increased inflammation
  • Participant may be receiving standard treatment for high blood pressure, high cholesterol, diabetes, kidney and heart problems
  • Participant may have ongoing kidney disease or heart failure

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

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (14)

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

SiteCityCountrySite status
Velocity Clinical Research Germany GmbH
Coordinator of this site? Confirm its status
BerlinGermanyRecruiting
Charite Universitaetsmedizin Berlin KöR
Coordinator of this site? Confirm its status
BerlinGermanyRecruiting
Klinisches Forschungszentrum Dr. Hagemann
Coordinator of this site? Confirm its status
EssenGermanyRecruiting
Medical Center- University of Freiburg
Coordinator of this site? Confirm its status
Freiburg im BreisgauGermanyRecruiting
Hausarztzentrum Butendorf
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GladbeckGermanyRecruiting
Kardiopraxis Schirmer
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KaiserslauternGermanyRecruiting
Klinikum Konstanz GmbH
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KonstanzGermanyRecruiting
Universitaetsklinikum Leipzig Aor
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LeipzigGermanyRecruiting
Gemeinschaftspraxis Dr. Jens Biesenbaum/Dr. Uwe Gerbaulet
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LoehneGermanyRecruiting
Haus der Gesundheit
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LudwigshafenGermanyRecruiting
ze:ro Praxen MVZ fuer Nierenerkrankungen und Bluthochdruck GmbH Mannheim
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MannheimGermanyRecruiting
Diabetologische Schwerpunktpraxis Pirna Hausärztliche Versorgung
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PirnaGermanyRecruiting
Robert Bosch Gesellschaft fuer medizinische Forschung mbH
Coordinator of this site? Confirm its status
StuttgartGermanyRecruiting
Cardiologicum Herzklinik Ulm MVZ GmbH
Coordinator of this site? Confirm its status
UlmGermanyRecruiting

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