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Taking people in ArgentinaPhase 3

Tests zilebesiran in adults with high-risk heart disease and high blood pressure

Tests zilebesiran against placebo in adults with uncontrolled high blood pressure and heart risk.

Plain-language title generated from the registry record
Registry title: Zilebesiran in Patients With Hypertension Not Adequately Controlled and With Either Established Cardiovascular Disease or High Risk for Cardiovascular Disease

Key facts

Where
Bahía Blanca, Buenos Aires, Ciudad Autónoma Buenos Aires, Ciudadela, Córdoba, Coronel Suárez, Corrientes, Esperanza, Formosa, General San Martín, Granadero Baigorria, Lanús Este, Mar del Plata, Morón, Quilmes, Ramos Mejía, Río Cuarto, Rosario, Salta, San Juan Bautista, San Miguel de Tucumán, San Nicolás de los Arroyos, Santa Fe, Temperley, and Villa María, ArgentinaSee the 25 sites
Phase
Phase 3

Where in Argentina

  • Bahía BlancaBahía Blanca, ArgentinaTaking people
  • Buenos AiresBuenos Aires, ArgentinaTaking people
  • Ciudad Autónoma Buenos AiresCiudad Autónoma Buenos Aires, ArgentinaTaking people
  • CiudadelaCiudadela, ArgentinaTaking people
  • CórdobaCórdoba, ArgentinaTaking people
  • Coronel SuárezCoronel Suárez, ArgentinaTaking people
  • CorrientesCorrientes, ArgentinaTaking people
  • EsperanzaEsperanza, ArgentinaTaking people
  • FormosaFormosa, ArgentinaTaking people
  • General San MartínGeneral San Martín, ArgentinaTaking people
  • Granadero BaigorriaGranadero Baigorria, ArgentinaTaking people
  • Lanús EsteLanús Este, ArgentinaTaking people
  • Mar del PlataMar del Plata, ArgentinaTaking people
  • MorónMorón, ArgentinaTaking people
  • QuilmesQuilmes, ArgentinaTaking people
  • Ramos MejíaRamos Mejía, ArgentinaTaking people
  • Río CuartoRío Cuarto, ArgentinaTaking people
  • RosarioRosario, ArgentinaTaking people
  • SaltaSalta, ArgentinaTaking people
  • San Juan BautistaSan Juan Bautista, ArgentinaTaking people
  • San Miguel de TucumánSan Miguel de Tucumán, ArgentinaTaking people
  • San Nicolás de los ArroyosSan Nicolás de los Arroyos, ArgentinaTaking people
  • Santa FeSanta Fe, ArgentinaTaking people
  • TemperleyTemperley, ArgentinaTaking people
  • Villa MaríaVilla María, ArgentinaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Alnylam Pharmaceuticals
Trial code
NCT07181109EU 2025-522960-34-00
Record updated
15 October 2026
Original description
The purpose of this study is to evaluate whether zilebesiran versus placebo reduces the risk of cardiovascular (CV) death, nonfatal myocardial infarction (MI), nonfatal stroke, or heart failure (HF) events. This is an event-driven study that will continue until the targeted number of positively adjudicated primary endpoint clinical outcome events (COEs) have been reached.Read full original descriptionShow less

ZENITH: A Phase 3 Global, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Zilebesiran in Addition to Standard of Care in Reducing Major Adverse Cardiovascular Events in Adult Patients With Hypertension Not Adequately Controlled and With Either Established Cardiovascular Disease or High Risk for Cardiovascular Disease

The purpose of this study is to evaluate whether zilebesiran versus placebo reduces the risk of cardiovascular (CV) death, nonfatal myocardial infarction (MI), nonfatal stroke, or heart failure (HF) events. This is an event-driven study that will continue until the targeted number of positively adjudicated primary endpoint clinical outcome events (COEs) have been reached.

Inclusion: Is 18 years or older for patients with established cardiovascular disease (CVD); Is 55 years or older for patients with high risk for CVD; Has established CVD (defined as coronary, cerebrovascular, or peripheral artery disease) or high risk for CVD; Has treated hypertension on stable therapy with at least 2 standard of care antihypertensive medications, one of which must be a thiazide, thiazide-like, or loop diuretic.

Exclusion: Has known history of secondary hypertension; Has alanine aminotransferase (ALT) or aspartate aminotransferase (AST) >3×upper limit of normal (ULN); Has total serum bilirubin >1.5×ULN; Has international normalized ratio (INR) >1.5; Has serum potassium >4.8 mEq/L; Has estimated glomerular filtration rate (eGFR) <30 mL/min/1.73m\^2; Has symptomatic orthostatic hypotension.

ClinicalTrials.gov NCT07181109 · EU CTIS 2025-522960-34-00