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A Study to Investigate the Efficacy, Safety, and Tolerability of DFV890 for Inflammatory Marker Reduction in Adult Participants With Coronary Heart Disease and Elevated hsCRP

NCT06031844

CompletedPhase 2

Sponsor: Novartis Pharmaceuticals

Conditions: Coronary Heart Disease

Interventions: DFV890, DFV890 Placebo

Countries: United States, Canada

This Phase 2a clinical trial evaluated the effectiveness, safety, and tolerability of increasing dose strengths of an oral daily medication, DFV890, administered for 12 weeks, to reduce key markers of inflammation related to CVD risk, such as IL-6 and IL-18, in approximately 24 people with known heart disease and an elevated marker of inflammation, hsCRP.

Eligibility overview

Sex: ALL

Age: 18 Years to 85 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria

Inclusion Criteria:

* Male and female participants aged between 18 - 85 years (inclusive) at the start of screening will be included.
* Subjects must have a body mass index (BMI) within the range of 18 - 45 kg/m2. BMI = Body weight (kg) / \[Height (m)\]2
* Documented spontaneous myocardial infarction (MI) (diagnosed according to the universal MI criteria with or without evidence of ST segment elevation) at least 30 days before the start of screening.
* Participants must have hsCRP levels ≥ 2 mg/L at two timepoints during screening. Screening values must be separated by a minimum of 8 days. The initial hsCRP value must be a minimum of 30 days after the qualifying MI or after any percutaneous coronary intervention (PCI) performed separately from the qualifying MI.
* For participants on statin therapy (HMG-CoA reductase inhibitor), as clinically indicated, participants must be on a stable regimen (at least 4 weeks before randomization), with no planned statin dose changes over the course of the trial treatment period. Unplanned statin dose changes during the trial treatment period may occur.

Exclusion Criteria:

* Patients receiving concomitant medications that are known to be strong or moderate inducers of cytochrome CYP2C9 enzyme and/or strong inducers of CYP3A, strong inhibitors of CYP2C9 and/or strong or moderate inhibitors of CYP3A and the treatment cannot be discontinued or switched to a different medication within 5 half-lives or 1 week (whichever is longer) prior to Day 1 and for the duration of the study.
* Patients with suspected or proven immunocompromised state at screening
* History of ongoing, chronic, or major recurrent infectious disease, at the discretion of the investigator, at the start of screening.
* Use of any biologic drugs targeting the immune system within 26 weeks of Day 1
* Multi-vessel Coronary Artery Bypass Graft (CABG) surgery within the past 6 months prior to the start of screening.
* Symptomatic Class IV heart failure (New York Heart Association) at the start of screening.
* Planned coronary revascularization (PCI or CABG) or any other major surgical procedure during the study.

Locations (7)

Northridge, California, United States
Boca Raton, Florida, United States
Jacksonville, Florida, United States
Greensboro, North Carolina, United States
Rapid City, South Dakota, United States
Tacoma, Washington, United States
Montreal, Quebec, Canada