Rationale and design of the Virginia Commonwealth University-Anakinra Remodeling Trial-3 (VCU-ART3): A randomized, placebo-controlled, double-blinded, multicenter study.
Benjamin W Van TassellMichael J LipinskiDarryn AppletonCharlotte S RobertsMichael C KontosNayef AbouzakiRyan MelchiorGeorge MuellerJames GarnettJustin CanadaSalvatore CarboneLeo F BuckleyGeorge WohlfordDinesh KadariyaCory R TrankleClaudia Oddi ErdleRobin SculthorpeLaura PuckettChristine DeWildeKeyur ShahDominick J AngiolilloGeorge VetrovecGiuseppe Biondi-ZoccaiRoss ArenaAntonio AbbatePublished in: Clinical cardiology (2018)
There is clear association between the intensity of the acute inflammatory response during acute myocardial infarction (AMI) and adverse prognosis after AMI. Interleukin-1 (IL-1) is a pro-inflammatory cytokine released during AMI and involved in adverse remodeling and heart failure (HF). We describe a study to evaluate the safety and efficacy of IL-1 blockade using an IL-1 receptor antagonist (anakinra) during the acute phase of ST-segment elevation myocardial infarction (STEMI). The Virginia Commonwealth University-Anakinra Remodeling Trial-3 (VCU-ART3; http://www.ClinicalTrials.gov NCT01950299) is a phase 2, multicenter, double-blinded, randomized, placebo-controlled clinical trial comparing anakinra 100 mg once or twice daily vs matching placebo (1:1:1) for 14 days in 99 patients with STEMI. Patients who present to the hospital with STEMI within 12 hours of symptom onset will be eligible for enrollment. Patients will be excluded for a history of HF (functional class III-IV), severe valvular disease, severe kidney disease (stage 4-5), active infection, recent use of immunosuppressive drugs, active malignancy, or chronic autoimmune/auto-inflammatory diseases. We will measure the difference in the area under the curve for C-reactive protein between admission and day 14, separately comparing each of the anakinra groups with the placebo group. The P value will be considered significant if <0.025 to adjust for multiple comparisons. Patients will also be followed for up to 12 months from enrollment to evaluate cardiac remodeling (echocardiography), cardiac function (echocardiography), and major adverse cardiovascular outcomes (cardiovascular death, MI, revascularization, and new onset of HF).
Keyphrases
- double blind
- acute myocardial infarction
- percutaneous coronary intervention
- placebo controlled
- phase iii
- st segment elevation myocardial infarction
- clinical trial
- phase ii
- left ventricular
- end stage renal disease
- heart failure
- study protocol
- inflammatory response
- open label
- st elevation myocardial infarction
- coronary artery disease
- acute coronary syndrome
- ejection fraction
- chronic kidney disease
- squamous cell carcinoma
- drug induced
- atrial fibrillation
- peritoneal dialysis
- computed tomography
- pulmonary hypertension
- prognostic factors
- coronary artery bypass grafting
- randomized controlled trial
- newly diagnosed
- physical activity
- early onset
- oxidative stress
- high intensity
- toll like receptor
- aortic valve
- hiv infected
- adverse drug
- acute care
- respiratory failure
- lipopolysaccharide induced
- acute respiratory distress syndrome
- locally advanced