Obicetrapib for Health & Longevity

Created on 10/28/2026 – Quick Reference based on Evidence Review created using AI4L / Opus 5.5 – Audit

Obicetrapib is an oral prescription medication that lowers artery-clogging cholesterol, approved in Europe in 2026. For health-focused adults above target despite treatment, or intolerant of standard cholesterol tablets, it offers a well-documented, injection-free drop. Benefit on heart attacks and strokes is not yet established; diabetes, kidney and brain hints rest on limited evidence. Short-term side-effect rates resemble an inactive tablet; an eye-disease question is unresolved; almost all evidence is developer-funded. (Full Review)

Protocol

Standard dose
10 mg once daily
Dose tested in phase 3; approved in Europe, as reported by the developer
Fixed-dose combination
Obicetrapib 10 mg plus ezetimibe 10 mg
One tablet (Evlarco), taken once daily
Time of day
Any consistent time
A high-fat meal raised exposure 1.6-fold, judged clinically irrelevant
Time to effect
LDL cholesterol reduction
8–12 weeks
Near maximal by this point
Cardiovascular events
After 6 months
Pooled event reduction; unconfirmed until the outcome trial reports
Steady state
Roughly 4 weeks
Half-life of about 131 hours; missed doses matter little

Benefits

Contraindications
  • Children and adolescents
  • Pregnancy and breastfeeding
  • Existing intermediate or advanced AMD
  • Severe hepatic impairment (Child-Pugh Class C)
Key Interactions
  • Statins (atorvastatin, rosuvastatin): additive LDL-C lowering
  • Ezetimibe: additive LDL-C lowering
Theoretical (inferred from mechanism)
  • PCSK9 inhibitors (evolocumab) and bempedoic acid: very low LDL-C
  • Red yeast rice (monacolin K): larger LDL-C drop plus statin-like muscle effects
  • Berberine: larger LDL-C drop
  • Plant sterols/stanols and psyllium: modestly larger LDL-C drop
  • Strong CYP3A4 inhibitors (ketoconazole) and inducers (rifampin): higher exposure or weaker LDL-C lowering
  • Non-steroidal anti-inflammatory drugs (ibuprofen) and oral decongestants (pseudoephedrine): higher blood pressure
  • Lutein and zeaxanthin supplements: unknown change in retinal antioxidant delivery

Risk & Side Effects

  • High:
  • Medium: Dizziness, headache and gastrointestinal adverse events
  • Low: Hypertension; age-related macular degeneration; muscle pain
  • Speculative: Unknown long-term and rare effects; altered transport of fat-soluble antioxidants

Monitoring

Marker Target Why
LDL-C <55 mg/dL (very high cardiovascular risk) Main efficacy marker
ApoB <65 mg/dL (very high cardiovascular risk) Best marker of artery-clogging particle number
Non-HDL cholesterol <85 mg/dL (very high cardiovascular risk) Total artery-clogging cholesterol
Lp(a) <75 nmol/L (<30 mg/dL); change from own baseline Expected to fall about 35–45%
HDL-C ≥40 mg/dL in men, ≥50 mg/dL in women; roughly a doubling from own baseline Confirms drug exposure and adherence
HbA1c 4.0–5.6% May improve; also a safety check
Fasting glucose Not specified in the ER Usual paired test with HbA1c
Creatinine / eGFR ≥60 mL/min/1.73 m² Safety check
ALT / AST ALT 7–56 U/L; AST 8–48 U/L Safety check: a sustained rise changes use
Creatine kinase About 30–200 U/L Safety check if muscle pain appears
Blood pressure No sustained rise Hypertension reported in trials

Cadence: Baseline before starting, including a week of home blood-pressure readings and a dilated retinal exam or retinal scan; lipids, apoB and blood pressure at 4–8 weeks, then every 6–12 months; HbA1c, eGFR and liver enzymes every 6–12 months; creatine kinase only if muscle symptoms appear; retinal examination every 1–2 years.

Qualitative Assessment

  • Dizziness or headache, especially in the first weeks
  • Bowel changes or abdominal pain
  • New muscle pain or weakness
  • Vision changes: central blurring, distorted straight lines or reduced color contrast
  • Symptoms of high blood pressure, such as morning headaches