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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05030428
Other study ID # CKJX839B12302
Secondary ID
Status Active, not recruiting
Phase Phase 3
First received
Last updated
Start date November 23, 2021
Est. completion date October 13, 2027

Study information

Verified date February 2024
Source Novartis
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Study CKJX839B12302 is a pivotal Phase III trial to evaluate the benefits of inclisiran on major adverse cardiovascular (MACE) events in participants with established cardiovascular disease (CVD).


Description:

Purpose of this study is to test the hypothesis that treatment with inclisiran sodium 300 mg s.c. administered on Day 1, Month 3 (Day 90), and every 6 months thereafter taken in addition to well-tolerated high-intensity statin therapy in participants with established ASCVD will significantly reduce the risk of 3-Point-Major Adverse Cardiovascular Events (3P-MACE) defined as a composite of CV death, non-fatal myocardial infarction (MI) and non-fatal ischemic stroke. This will be compared to placebo in adjunct to well-tolerated high-intensity statin therapy.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 17013
Est. completion date October 13, 2027
Est. primary completion date October 13, 2027
Accepts healthy volunteers No
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria: 1. Fasting LDL-C = 70 mg/dL at randomization visit 2. Stable (greater than or equal to 4 weeks) and well-tolerated lipid-lowering regimen (including e.g. with or without Ezetimibe) that must include a high-intensity statin therapy with either atorvastatin greater than or equal to 40 mg QD or rosuvastatin greater than or equal to 20 mg QD 3. Established CV disease defined as ANY of the following three conditions 1. Spontaneous Myocardial infarction = 4 weeks from screening visit 2. History of ischemic stroke occurred = 4 weeks prior to the Screening visit 3. Symptomatic peripheral arterial disease (PAD) evidenced by either intermittent claudication with ankle brachial index (ABI) < 0.85, prior peripheral arterial revascularization procedure, or, amputation due to atherosclerotic disease. Exclusion Criteria: 1. Acute coronary syndrome, stroke, peripheral arterial revascularization procedure or amputation due to atherosclerotic disease < 4 weeks before screening visit 2. Treatment with PCSK9 inhibitors (e.g. evolocumab, alirocumab) within 90 days or planned use post first study visit 3. Planned or expected cardiac, cerebrovascular or peripheral artery surgery or re-vascularization within the 6 months after the first study visit 4. Heart failure NYHA class III or IV 5. Active liver disease defined as any known current infectious, neoplastic, or metabolic pathology of the liver 6. Previous exposure to inclisiran or any other non-mAb PCSK9-targeted therapy, either as an investigational or marketed drug within 2 years 7. Severe concomitant non-CV disease that is expected to reduce life expectancy to less than 5 years 8. History of malignancy that required surgery radiation therapy and/or systemic therapy during the 3 years prior to the first study visit 9. Pregnant or nursing (lactating) women Other protocol-defined inclusion/exclusion criteria may apply.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Inclisiran sodium 300 mg
Subcutaneously injected on Day 1, Month 3 (Day 90) and every 6 months thereafter until EOS visit
Placebo
Subcutaneously injected on Day 1, Month 3 (Day 90) and every 6 months thereafter until EOS visit

Locations

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United States Jefferson Abington Abington Pennsylvania
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United States Alaska Cardiology Reserach Foundation, NFP Anchorage Alaska
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United States Northwest Heart Clinical Research LLC Arlington Heights Illinois
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United States Central Cardiology Medical Center Bakersfield California
United States Sinai Ct for Throm Res and Drug Dev Baltimore Maryland
United States Louisiana Cardiology Associates Baton Rouge Louisiana
United States Pennington Biomedical Research Center Baton Rouge Louisiana
United States North Hills Medical Research, Inc . Bedford Texas
United States Metropolitan Cardiovascular Consultants LLC Beltsville Maryland
United States Belzoni Clinical Research Belzoni Mississippi
United States Bend Memorial Clinic Bend Oregon
United States Meridian Clinical Research Binghamton New York
United States Ascension St Vincent's . Birmingham Alabama
United States Excel Medical Clinical Trials LLC Boca Raton Florida
United States Grace Research LLC Bossier City Louisiana
United States Beth Israel Deaconess Medical Ce . Boston Massachusetts
United States Tufts Medical Center Main Centre Boston Massachusetts
United States VA Boston Healthcare System Jamaica Plain Division Boston Massachusetts
United States Progressive Clinical Research Bountiful Utah
United States Cardiovascular and Vein Center of Florida Bradenton Florida
United States Nova Clinical Research LLC . Bradenton Florida
United States Bridgeport Hospital Bridgeport Connecticut
United States Burke Internal Medicine and Research Burke Virginia
United States Butler Memorial Hospital Butler Pennsylvania
United States Hope Clinical Research . Canoga Park California
United States Medical Univ of South Carolina CTBM100C2407 Charleston South Carolina
United States Novant Health Heart and Vascular Institute Charlotte North Carolina
United States Novant Health Heart and Vascular Institute . Charlotte North Carolina
United States Cedar Crosse Research Ct Chicago Illinois
United States Chicago Clinical Research Institute Inc Chicago Illinois
United States Meridian Clinical Research Cincinnati Ohio
United States University of Cincinnati . Cincinnati Ohio
United States Bay Care Medical Group Clearwater Florida
United States University Hospitals Cleveland Medical Center Univ. Hospitals of Cleveland Cleveland Ohio
United States Columbia Heart Clinic Columbia South Carolina
United States Columbia VA Health Care System Columbia South Carolina
United States Johns Hopkins University Columbia Maryland
United States John Muir Physician Network Clinical Research Center Concord California
United States Bassett Medical Center Cooperstown New York
United States Samaritan Cardiology Corvallis Oregon
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United States Cardiology Research Associates Daytona Beach Florida
United States Hillcrest Medical Research DeLand Florida
United States Aurora Denver Cardiology Associates Denver Colorado
United States Henry Ford Hospital Detroit Michigan
United States St Marys Medical Center Duluth Minnesota
United States APRC, Inc Dunwoody Georgia
United States Monmouth Cardiology Associates Eatontown New Jersey
United States David Turbay MD PLLC El Paso Texas
United States Elkhart Cardiology Group Elkhart Indiana
United States Meridian Clinical Research LLC Endwell New York
United States Horizon Research Group of Opelousas, LLC Eunice Louisiana
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United States Javara Research . Fayetteville Georgia
United States Javara Research South Coast Health Fayetteville Georgia
United States AA Medical Research Center Flint Michigan
United States G and L Research LLC Foley Alabama
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United States Texas Health Physicians Group Fort Worth Texas
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United States The Heart Group Cardiovascular Associates Inc Fresno California
United States ASCADA Research Fullerton California
United States Northeast Georgia Medical Center Gainesville Georgia
United States Mercy Gilbert Medical Center Gilbert Arizona
United States Javara Inc . Glenn Dale Maryland
United States Altru Health Research Dept. Grand Forks North Dakota
United States Healthy Heart Cardiology Grand Rapids Michigan
United States Cardiovascular Institute South ASC Gray Louisiana
United States Prisma Health Upstate . Greenville South Carolina
United States Upstate Cardiology Greenville South Carolina
United States Wellmont CVA Heart Institute Greenville Tennessee
United States d-b-a Greenwich Cardio Assoc Greenwich Connecticut
United States Cooper University Health Care . Haddon Heights New Jersey
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United States Heart Care Associates, P.C. Hopewell Virginia
United States Cardiovascular Institute of the South Dept of Cardiovascular Inst Houma Louisiana
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United States Houston Methodist Hospital . Houston Texas
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United States UT Physicians Memorial Hermann Houston Texas
United States Village Medical Village MD S Tx Houston Texas
United States Diabetes/Lipid Management Center Huntington Beach California
United States Franciscan Health Services Research Center . Indianapolis Indiana
United States University of Calif Irvine Med Cntr Irvine California
United States Apex Cardiology Research Associates of Jackson Jackson Tennessee
United States Jackson Heart Clinic Jackson Mississippi
United States The Jackson Clinic PA Research Jackson Tennessee
United States VAMC Research-G V Sonny Montgomery Clinic Jackson Mississippi
United States University of Florida - Shands Jacksonville UF Health Jacksonville Jacksonville Florida
United States Westside Center for Clinical Research . Jacksonville Florida
United States Baptist Heart Specialists Jacksonville Beach Florida
United States Gateway Cardiology PC Jerseyville Illinois
United States Kansas City VA Medical Center Kansas City Missouri
United States University of Kansas Medical Center . Kansas City Kansas
United States Kettering Medical Center Kettering Ohio
United States Accellacare . Knoxville Tennessee
United States Turkey Creek Medical Center Knoxville Tennessee
United States Turkey Creek Medical Center . Knoxville Tennessee
United States UC San Diego Health Altman Clin Trnsltnl Res Inst La Jolla California
United States Trident Cardiology Ladson South Carolina
United States Cardiovascular Institute of the South Lafayette Louisiana
United States United Vein and Vascular Centers Lake Worth Florida
United States FMC Science Research Lampasas Texas
United States Capitol Cardiology Associates Lanham Maryland
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United States Clinical Research of South Nevada . Las Vegas Nevada
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United States University of Kentucky College of Health Sciences . Lexington Kentucky
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United States Arkansas Clinical Research Little Rock Arkansas
United States East Texas Research Associates Inc. Livingston Texas
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United States Keck Medical Center USC Keck School of Medicine of USC Los Angeles California
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United States Discovery Clinical Trials McAllen Texas
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United States North Kansas City Hospital North Kansas City Missouri
United States Northport VA Medical Center Northport New York
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United States Methodist Physicians Clinic Heart Consultants Omaha Nebraska
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United States Cabrillo Cardiology Medical Group Oxnard California
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United States VA Palo Alto Health Care System . Palo Alto California
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United States Dominion Medical Associates Richmond Virginia
United States The Valley Hospital Ridgewood New Jersey
United States Roanoke Heart Institute Roanoke Virginia
United States North Memorial Heart and Vascular Institute Robbinsdale Minnesota
United States Rochester Clinical Research Rochester New York
United States Adventist HealthCare Shady Grove Medical Center Rockville Maryland
United States Ascension St Marys Hospital Saginaw Michigan
United States CentraCare Heart and Vascular Center Saint Cloud Minnesota
United States Gateway Cardiovascular Rsch Ctr Inc Saint Louis Missouri
United States Mercy South . Saint Louis Missouri
United States St Louis Heart and Vascular . Saint Louis Missouri
United States St Louis V A Medical Center . Saint Louis Missouri
United States Regions Hospital Main Center Saint Paul Minnesota
United States Advanced Medical Research Center Saint Petersburg Florida
United States Accellacare Salisbury North Carolina
United States Tidal Health Peninsula Regional Inc Salisbury Maryland
United States Endeavor Clinical Trials . San Antonio Texas
United States Sou Tx Cardiovascular Consu PLLC . San Antonio Texas
United States University of Texas Health Science Center at San Antonio . San Antonio Texas
United States San Diego Veterans Medical Center San Diego California
United States Javara Research San Marcos Texas
United States West Coast Research LLC . San Ramon California
United States Helping Hands Medical Associates, INC Santa Ana California
United States Syrentis Clinical Research Santa Ana California
United States HonorHealth Heart Group Deer Valley . Scottsdale Arizona
United States Swedish Medical Ctr Cardiovascular Re Seattle Washington
United States University of Washington Clin Atherosclerosis Res Lab Seattle Washington
United States Virginia Mason Medical Centre Seattle Washington
United States Sherman Clinical Research Sherman Texas
United States Grace Research Llc Shreveport Louisiana
United States North Central Heart . Sioux Falls South Dakota
United States Sanford University of South Dakota Medical Center Sanford Cardiovascular Institu Sioux Falls South Dakota
United States Louisiana Heart Center Research Slidell Louisiana
United States Frontier Clinical Research LLC Smithfield Pennsylvania
United States Cardio Metabolic Institute CACZ885M2301 Somerset New Jersey
United States Providence Hospital Patient Care Research Southfield Michigan
United States Encompass Clinical Research . Spring Valley California
United States Heart House Research Foundation Springfield Ohio
United States Mercy Hospital . Springfield Missouri
United States Prairie Heart Institute Springfield Illinois
United States SIU School of Medicine Springfield Illinois
United States Stanford University Medical Center School of Medicine Stanford California
United States Stephenville Med and Surgical Stephenville Texas
United States Manshadi Heart Institute Stockton California
United States State Uni of NY at Stony Brook Stony Brook New York
United States Privia Medical Group Gulf Coast Sugar Land Texas
United States Clinical Research Inst of Arizona Sun City West Arizona
United States Universal Research Group LLC Suite 202 Tacoma Washington
United States BayCare Health System . Tampa Florida
United States BayCare Medical Group Inc Tampa Florida
United States Genesis Clinical Research Tampa Florida
United States James A Haley Veterans Hospital . Tampa Florida
United States New Tampa Health Tampa Florida
United States Ravessa Clinical Research Tampa Florida
United States Javara Research The Woodlands Texas
United States Mercy Health St Vincent Med Ctr Toledo Ohio
United States Cotton-O'Neil Clinical Research Center Topeka Kansas
United States University of California at Los Angeles Torrance California
United States Traverse Heart and Vascular Traverse City Michigan
United States Atlanta Heart Specialists LLC Main Center Tucker Georgia
United States Pima Heart And Vascular Clin Rch . Tucson Arizona
United States Tennessee Center for Clinical Trials Tullahoma Tennessee
United States Oklahoma Heart Institute . Tulsa Oklahoma
United States Cardiology Associates of North MS Tupelo Mississippi
United States Tilda Research Tustin California
United States Preferred Primary Care Physicians, Inc. Uniontown Pennsylvania
United States Westchester Medical Center . Valhalla New York
United States Premier Cardiovascular Institute Vandalia Ohio
United States Blue Coast Research Center LLC Vista California
United States Kent County Memorial Hospital Warwick Rhode Island
United States Emerson Clinical Research Institute, LLC Washington District of Columbia
United States Washington Hospital Center Medstar Washington District of Columbia
United States Chase Medical Research, LLC Waterbury Connecticut
United States Covenant Medical Center MercyOne Waterloo Med Ct Waterloo Iowa
United States Cardiology Partners Clinical Research Institute Wellington Florida
* Note: There are 1010 locations in all - only the first 1000 are shown.

Sponsors (1)

Lead Sponsor Collaborator
Novartis Pharmaceuticals

Countries where clinical trial is conducted

United States,  Argentina,  Australia,  Austria,  Belgium,  Brazil,  Bulgaria,  Canada,  Chile,  China,  Colombia,  Croatia,  Czechia,  Denmark,  Estonia,  Finland,  France,  Greece,  Hungary,  Iceland,  India,  Israel,  Italy,  Japan,  Kenya,  Korea, Republic of,  Latvia,  Lithuania,  Malaysia,  Mauritius,  Mexico,  Netherlands,  New Zealand,  Norway,  Philippines,  Poland,  Portugal,  Puerto Rico,  Romania,  Russian Federation,  Serbia,  Singapore,  Slovakia,  Slovenia,  South Africa,  Spain,  Sweden,  Taiwan,  Thailand,  Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time to First Occurrence of 3P-MACE (3-Point Major Adverse Cardiovascular Events) 3P-MACE is a confirmed composite endpoint which includes cardiovascular death, non-fatal myocardial infarction and non-fatal ischemic stroke. From randomization to total follow-up time (up to 72 months)
Secondary Time to Occurrence of Cardiovascular (CV) Death CV death is defined as death due to cardiovascular events From randomization to total follow-up time (up to 72 months)
Secondary Time to First Occurrence of 4P-MACE (4-Point Major Adverse Cardiovascular Events) A composite 4P- MACE is defined as CV death, non-fatal MI, non-fatal ischemic stroke and urgent coronary revascularization. From randomization to total follow-up time (up to 72 months)
Secondary Time to first occurrence of Major Limb Adverse Events (MALE) Major Limb Adverse Events including acute lower limb ischemia, lower limb amputation due to ischemia, or urgent lower limb revascularization for ischemia From randomization to total follow-up time (up to 72 months)
Secondary Time to occurrence of all-cause death All-Cause death is defined as: all deaths from randomization until up to 72 months From randomization to total follow-up time (up to 72 months)
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