Phase 2
N=24
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
Coronary Heart Disease
Bottom Line
View on ClinicalTrials.gov: NCT06031844 ↗Enrolled (actual)
24
Serious AEs
1.5%
Results posted
Mar 2026
Primary outcome: Primary: Ratio to Baseline Serum Levels of IL-6 for DFV890 Based on an Emax Model — 0.7191; 0.5478; 0.4512; 0.3901 ratio serum levels of IL-6 — p=0.0011
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- DFV890 (Drug); DFV890 Placebo (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Novartis Pharmaceuticals
- Primary completion
- Dec 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Ratio to Baseline Serum Levels of IL-6 for DFV890 Based on an Emax Model |
0.7191; 0.5478; 0.4512; 0.3901; 1.0828 | 0.0011 sig |
| PRIMARY Ratio to Baseline Serum Levels of IL-18 for DFV890 Based on an Emax Model |
0.9334; 0.8944; 0.8676; 0.8481; 0.9956 | 0.0108 sig |
| SECONDARY Trough Plasma Concentration (Ctrough) |
146; 455; 898; 2050 | — |
Summary
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 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.
Data sourced from ClinicalTrials.gov (NCT06031844). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.