← Back
NeuroTrials.ai
Neurology Clinical Trial Database

CORALreef Lipids

A Placebo-Controlled Trial of the Oral PCSK9 Inhibitor Enlicitide

Year of Publication: 2026

Authors: Ann Marie Navar, Elina Mikhailova, Alberico L. Catapano, ..., Christie M. Ballantyne; for the CORALreef Lipids Investigators

Journal: New England Journal of Medicine

Citation: N Engl J Med 2026;394:529-39. DOI: 10.1056/NEJMoa2511002

Link: https://clinicaltrials.gov/ct2/show/NCT05952856


Clinical Question

Does the oral PCSK9 inhibitor enlicitide effectively lower LDL cholesterol levels compared to placebo in adults with established atherosclerotic cardiovascular disease or at high risk for a first ASCVD event?

Bottom Line

Once-daily oral enlicitide 20 mg reduced LDL cholesterol by approximately 56–60 percentage points compared to placebo at 24 weeks, with 67.5% of patients achieving LDL-C <55 mg/dL with ≥50% reduction. The drug also significantly lowered non-HDL cholesterol, apolipoprotein B, and lipoprotein(a), with no apparent increase in adverse events. This oral PCSK9 inhibitor offers efficacy comparable to injectable anti-PCSK9 monoclonal antibodies.

Major Points

  • First phase 3 trial of an oral PCSK9 inhibitor (enlicitide decanoate) for LDL-C lowering
  • Enlicitide reduced LDL-C by 57.1% vs +3.0% increase with placebo at 24 weeks (adjusted difference −55.8 pp, p<0.001)
  • Effect sustained at 52 weeks with adjusted difference of −47.6 percentage points
  • Comparable LDL-C reduction to injectable PCSK9 inhibitors (alirocumab, evolocumab)
  • Non-HDL-C reduced by 53.4 pp, ApoB by 50.3 pp, and Lp(a) by 28.2 pp vs placebo
  • 67.5% achieved LDL-C <55 mg/dL with ≥50% reduction (vs 1.2% placebo)
  • No significant differences in adverse events, serious adverse events, or deaths
  • No increase in new-onset or worsening diabetes mellitus
  • High adherence (97.2%) to daily oral dosing with fasting requirements
  • Cardiovascular outcomes trial (CORALreef Outcomes) ongoing with projected completion December 2029

Design

Study Type: Phase 3, multinational, double-blind, randomized, placebo-controlled trial

Randomization: 1

Blinding: Double-blind; participants and investigators blinded to treatment assignment; matching placebo (note: placebo did not contain sodium caprate excipient)

Enrollment Period: August 2023 to July 2025

Follow-up Duration: 52 weeks treatment + 8 weeks safety follow-up

Centers: 168

Countries: USA, Japan, UK, Spain, Colombia, South Africa, Argentina, China, and others (14 countries total)

Sample Size: 2904

Analysis: Intention-to-treat; ANCOVA model with baseline value as covariate, treatment and stratification factors (renal function, geographic region) as fixed effects; washout imputation for missing data; nonparametric bootstrap (1000 samples) for CIs; aligned-rank Wilcoxon test for Lp(a); hierarchical testing for multiplicity control


Inclusion Criteria

  • Age ≥18 years
  • History of major ASCVD event (ACS, MI, coronary revascularization, ischemic stroke, cerebrovascular revascularization, or PAD with acute limb ischemia/revascularization/major amputation) with LDL-C ≥55 mg/dL
  • OR intermediate-to-high risk for first ASCVD event (heterozygous FH, diabetes, stable angina, prior TIA, symptomatic PAD, age ≥40 with 10-year ASCVD risk ≥7.5%, or CAC score ≥100) with LDL-C ≥70 mg/dL
  • Stable dose of appropriate lipid-lowering therapy for ≥30 days (including at least moderate- or high-intensity statin unless documented statin intolerance)

Exclusion Criteria

  • Active or recent treatment with a PCSK9 inhibitor
  • Uncontrolled hypertension
  • Uncontrolled diabetes
  • Active liver disease
  • Triglyceride level ≥400 mg/dL at screening

Arms

FieldEnlicitideControl
InterventionEnlicitide decanoate 20 mg oral tablet once daily, taken in the morning on an empty stomach with food/beverages (other than water) withheld for 30 minutes after dosing; formulation contains sodium caprate as permeation enhancerMatching placebo tablet once daily with same administration instructions; formulation did not contain sodium caprate
Duration52 weeks52 weeks

Outcomes

OutcomeTypeControlInterventionHR / OR / RRP-value
Mean percent change in LDL cholesterol level from baseline to week 24Primary+3.0% (95% CI 0.9 to 5.1)−57.1% (95% CI −61.8 to −52.5)<0.001
Mean percent change in LDL-C from baseline to week 52Secondary+4.0% (95% CI 1.7 to 6.3)−50.4% (95% CI −54.2 to −46.6)<0.001
Mean percent change in non-HDL-C from baseline to week 24Secondary+2.6% (95% CI 0.8 to 4.5)−53.7% (95% CI −55.0 to −52.5)<0.001
Mean percent change in ApoB from baseline to week 24Secondary+2.9% (95% CI 1.3 to 4.4)−49.6% (95% CI −50.8 to −48.5)<0.001
Median percent change in Lp(a) from baseline to week 24Secondary0.0% (IQR −14.9 to 13.3)−29.0% (IQR −50.4 to −7.0)<0.001
LDL-C <70 mg/dL with ≥50% reduction at week 24Secondary1.5%70.3%Not reported
LDL-C <55 mg/dL with ≥50% reduction at week 24Secondary1.2%67.5%Not reported
Any adverse eventAdverse602 (62.1%)1244 (64.3%)NS
Any serious adverse eventAdverse116 (12.0%)191 (9.9%)NS
Discontinuation due to adverse eventAdverse40 (4.1%)60 (3.1%)Not reported
DeathAdverse7 (0.7%)13 (0.7%)NS
New-onset or worsening diabetes mellitusAdverse56 (5.8%)119 (6.1%)NS
Drug-induced liver injuryAdverse00NA

Subgroup Analysis

Subgroup analyses for primary endpoint showed consistent LDL-C reduction across prespecified subgroups (Figure S3 in supplement). Results not detailed in main publication.


Criticisms

  • Efficacy results reflect clinical trial setting rather than real-world adherence
  • Protocol-prespecified data-handling rule for beta-quantification led to transformation of biologically impossible LDL-C values (≤0) to 1 mg/dL, underestimating treatment effect in primary analysis
  • 52-week follow-up is short relative to lifetime lipid-lowering therapy; long-term durability unknown
  • Missing data from deceased participants were imputed
  • Trial not powered to detect rare adverse events
  • Placebo formulation did not contain sodium caprate (permeation enhancer present in active drug), potentially affecting blinding
  • Cardiovascular outcomes not assessed — awaiting CORALreef Outcomes trial (projected completion 2029)
  • Requires fasting administration (30 min before food) which may affect real-world adherence

Funding

MSD (Rahway, NJ); Sponsor designed trial in collaboration with scientific advisory committee, performed data analysis, and participated in manuscript preparation

Based on: CORALreef Lipids (New England Journal of Medicine, 2026)

Authors: Ann Marie Navar, Elina Mikhailova, Alberico L. Catapano, ..., Christie M. Ballantyne; for the CORALreef Lipids Investigators

Citation: N Engl J Med 2026;394:529-39. DOI: 10.1056/NEJMoa2511002

Content summarized and formatted by NeuroTrials.ai.