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Efficacy and Safety of Alirocumab (SAR236553/REGN727) Versus Ezetimibe on Top of Statin in High Cardiovascular Risk Patients With Hypercholesterolemia (ODYSSEY COMBO II)

23. juni 2016 opdateret af: Sanofi

A Randomized, Double-Blind, Parallel Group Study to Evaluate the Efficacy and Safety of SAR236553/REGN727 Versus Ezetimibe in High Cardiovascular Risk Patients With Hypercholesterolemia Not Adequately Controlled With Their Statin Therapy

Alirocumab (SAR236553/REGN727) is a fully human monoclonal antibody that binds PCSK9 (proprotein convertase subtilisin/kexin type 9).

Primary Objective of the study:

To demonstrate the reduction of low-density lipoprotein cholesterol (LDL-C) by alirocumab as add-on therapy to stable maximally tolerated daily statin therapy in comparison with ezetimibe after 24 weeks of treatment in participants with hypercholesterolemia at high cardiovascular (CV) risk.

Secondary Objectives:

  • To evaluate the effect of alirocumab in comparison with ezetimibe on LDL-C at other time points
  • To evaluate the effect of alirocumab on other lipid parameters
  • To evaluate the safety and tolerability of alirocumab

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Detaljeret beskrivelse

The maximum study duration was 115 weeks per participant, including a 3-week screening period, 104-week randomized treatment period and 8-week follow-up period.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

720

Fase

  • Fase 3

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

  • Canada
      • Brampton, Canada, L6T 3J1
        • Investigational Site Number 124902
      • Mirabel, Canada, J7J 2K8
        • Investigational Site Number 124914
      • Montreal, Canada, H1T 3Y7
        • Investigational Site Number 124903
      • Toronto, Canada, M9V 4B4
        • Investigational Site Number 124918
  • Danmark
      • Esbjerg, Danmark, 6700
        • Investigational Site Number 208913
      • Glostrup, Danmark, 2600
        • Investigational Site Number 208914
      • Hellerup, Danmark, 2900
        • Investigational Site Number 208905
      • Herlev, Danmark, 2730
        • Investigational Site Number 208911
      • Hvidovre, Danmark, 2650
        • Investigational Site Number 208907
      • København S, Danmark, 2300
        • Investigational Site Number 208901
      • Køge, Danmark, 4600
        • Investigational Site Number 208906
      • Roskilde, Danmark, 4000
        • Investigational Site Number 208908
      • Silkeborg, Danmark, 8600
        • Investigational Site Number 208903
  • Den Russiske Føderation
      • Barnaul, Den Russiske Føderation, 656055
        • Investigational Site Number 643906
      • Kemerovo, Den Russiske Føderation, 650002
        • Investigational Site Number 643903
      • Moscow, Den Russiske Føderation, 111539
        • Investigational Site Number 643927
      • Moscow, Den Russiske Føderation, 111539
        • Investigational Site Number 643928
      • Moscow, Den Russiske Føderation, 115404
        • Investigational Site Number 643931
      • Moscow, Den Russiske Føderation, 119048
        • Investigational Site Number 643924
      • Moscow, Den Russiske Føderation, 121374
        • Investigational Site Number 643932
      • Moscow, Den Russiske Føderation, 121552
        • Investigational Site Number 643908
      • Moscow, Den Russiske Føderation, 129090
        • Investigational Site Number 643904
      • Orenburg, Den Russiske Føderation, 450000
        • Investigational Site Number 643911
      • Ryazan, Den Russiske Føderation, 390026
        • Investigational Site Number 643921
      • Saint-Petersburg, Den Russiske Føderation, 197110
        • Investigational Site Number 643925
      • Saint-Petersburg, Den Russiske Føderation, 198205
        • Investigational Site Number 643922
      • Saratov, Den Russiske Føderation, 410028
        • Investigational Site Number 643929
      • St-Petersburg, Den Russiske Føderation, 199106
        • Investigational Site Number 643914
  • Forenede Stater
    • Alabama
      • Birmingham, Alabama, Forenede Stater, 35209
        • Investigational Site Number 840980
    • Arizona
      • Phoenix, Arizona, Forenede Stater, 85032
        • Investigational Site Number 840918
      • Tucson, Arizona, Forenede Stater
        • Investigational Site Number 840925
    • California
      • Anaheim, California, Forenede Stater, 92801
        • Investigational Site Number 840959
      • Beverly Hills, California, Forenede Stater, 90211
        • Investigational Site Number 840301
      • Chino, California, Forenede Stater, 91710
        • Investigational Site Number 840933
      • Lincoln, California, Forenede Stater, 95648
        • Investigational Site Number 840991
      • Los Angeles, California, Forenede Stater, 90057
        • Investigational Site Number 840979
      • Palm Springs, California, Forenede Stater, 92262
        • Investigational Site Number 840952
      • Thousand Oaks, California, Forenede Stater, 91360
        • Investigational Site Number 840930
      • Vista, California, Forenede Stater, 92083
        • Investigational Site Number 840921
    • Florida
      • Boynton Beach, Florida, Forenede Stater, 33472
        • Investigational Site Number 840962
      • Bradenton, Florida, Forenede Stater, 34203
        • Investigational Site Number 840987
      • Clearwater, Florida, Forenede Stater, 33756
        • Investigational Site Number 840302
      • Jacksonville, Florida, Forenede Stater, 32223
        • Investigational Site Number 840935
      • Miami, Florida, Forenede Stater, 33126
        • Investigational Site Number 840903
      • Miami, Florida, Forenede Stater
        • Investigational Site Number 840920
      • Ocala, Florida, Forenede Stater, 34471
        • Investigational Site Number 840943
      • Oveido, Florida, Forenede Stater, 32765
        • Investigational Site Number 840981
      • Port Orange, Florida, Forenede Stater, 32127
        • Investigational Site Number 840961
      • Sarasota, Florida, Forenede Stater, 34239
        • Investigational Site Number 840303
      • St. Petersburg, Florida, Forenede Stater
        • Investigational Site Number 840986
      • St. Petersburg, Florida, Forenede Stater
        • Investigational Site Number 840988
    • Idaho
      • Meridian, Idaho, Forenede Stater, 83646
        • Investigational Site Number 840995
    • Indiana
      • Evansville, Indiana, Forenede Stater, 47714
        • Investigational Site Number 840902
    • Kansas
      • Topeka, Kansas, Forenede Stater, 66606
        • Investigational Site Number 840960
    • Maryland
      • Oxon Hill, Maryland, Forenede Stater, 20745
        • Investigational Site Number 840940
    • Massachusetts
      • Fall River, Massachusetts, Forenede Stater, 02720
        • Investigational Site Number 840966
    • Missouri
      • Kansas City, Missouri, Forenede Stater, 64114
        • Investigational Site Number 840917
      • St. Louis, Missouri, Forenede Stater, 63131
        • Investigational Site Number 840998
    • Montana
      • Butte, Montana, Forenede Stater, 59701
        • Investigational Site Number 840946
    • Nebraska
      • Lincoln, Nebraska, Forenede Stater, 68510
        • Investigational Site Number 840914
    • New Mexico
      • Albuquerque, New Mexico, Forenede Stater, 87106
        • Investigational Site Number 840949
    • New York
      • New Windsor, New York, Forenede Stater, 12553
        • Investigational Site Number 840974
    • North Carolina
      • Greenville, North Carolina, Forenede Stater, 27834
        • Investigational Site Number 840955
      • Lexington, North Carolina, Forenede Stater, 27292
        • Investigational Site Number 840938
      • Smithfield, North Carolina, Forenede Stater, 27577
        • Investigational Site Number 840976
      • Winston-Salem, North Carolina, Forenede Stater, 27103
        • Investigational Site Number 840985
    • Ohio
      • Cincinnati, Ohio, Forenede Stater, 45219
        • Investigational Site Number 840963
      • Lyndhust, Ohio, Forenede Stater, 44124
        • Investigational Site Number 840970
      • Marion, Ohio, Forenede Stater, 43302
        • Investigational Site Number 840906
      • Marion, Ohio, Forenede Stater, 43302
        • Investigational Site Number 840997
      • Perrysburg, Ohio, Forenede Stater, 43551
        • Investigational Site Number 840964
    • South Carolina
      • Charleston, South Carolina, Forenede Stater, 29412
        • Investigational Site Number 840913
      • Greer, South Carolina, Forenede Stater, 29651
        • Investigational Site Number 840912
      • Summerville, South Carolina, Forenede Stater, 29485
        • Investigational Site Number 840992
    • Tennessee
      • Bristol, Tennessee, Forenede Stater, 37620
        • Investigational Site Number 840932
      • Nashville, Tennessee, Forenede Stater, 37205
        • Investigational Site Number 840944
    • Texas
      • Fort Worth, Texas, Forenede Stater, 76104
        • Investigational Site Number 840994
      • Houston, Texas, Forenede Stater, 77070
        • Investigational Site Number 840973
      • Houston, Texas, Forenede Stater, 77074
        • Investigational Site Number 840939
      • Sugar Land, Texas, Forenede Stater, 77479
        • Investigational Site Number 840945
      • Tomball, Texas, Forenede Stater, 77375
        • Investigational Site Number 840971
    • Utah
      • Orem, Utah, Forenede Stater, 84058
        • Investigational Site Number 840982
    • Virginia
      • Norfolk, Virginia, Forenede Stater, 23502
        • Investigational Site Number 840931
      • Richmond, Virginia, Forenede Stater, 23227
        • Investigational Site Number 840984
    • Washington
      • Renton, Washington, Forenede Stater, 98055
        • Investigational Site Number 840928
      • Spokane, Washington, Forenede Stater, 99204
        • Investigational Site Number 840990
  • Frankrig
      • Dijon, Frankrig, 21079
        • Investigational Site Number 250906
      • Montpellier Cedex 5, Frankrig, 34295
        • Investigational Site Number 250907
      • Nantes, Frankrig, 44093
        • Investigational Site Number 250903
      • Nimes, Frankrig, 30900
        • Investigational Site Number 250905
  • Israel
      • Holon, Israel, 58100
        • Investigational Site Number 376908
      • Kfar Saba, Israel, 44281
        • Investigational Site Number 376903
      • Ofakim, Israel, 80300
        • Investigational Site Number 376906
      • Petach Tikva, Israel
        • Investigational Site Number 376902
      • Rehovot, Israel, 76100
        • Investigational Site Number 376904
      • Safed, Israel, 13100
        • Investigational Site Number 376907
      • Tel Aviv, Israel, 64239
        • Investigational Site Number 376901
  • Korea, Republikken
      • Anyang-Si, Korea, Republikken, 431-070
        • Investigational Site Number 410908
      • Busan, Korea, Republikken, 602-715
        • Investigational Site Number 410920
      • Daegu, Korea, Republikken, 700-712
        • Investigational Site Number 410926
      • Gwangju, Korea, Republikken, 501-757
        • Investigational Site Number 410923
      • Seoul, Korea, Republikken, 110-744
        • Investigational Site Number 410909
      • Seoul, Korea, Republikken, 120-752
        • Investigational Site Number 410922
      • Seoul, Korea, Republikken, 135-710
        • Investigational Site Number 410921
      • Seoul, Korea, Republikken, 135-720
        • Investigational Site Number 410905
      • Seoul, Korea, Republikken, 137-701
        • Investigational Site Number 410901
      • Seoul, Korea, Republikken, 138-736
        • Investigational Site Number 410914
      • Seoul, Korea, Republikken, 156-707
        • Investigational Site Number 410924
      • Suwon, Korea, Republikken, 443-721
        • Investigational Site Number 410915
      • Uijeongbu, Korea, Republikken, 480-717
        • Investigational Site Number 410913
      • Wonju, Korea, Republikken, 220-701
        • Investigational Site Number 410927
  • Sydafrika
      • Alberton, Sydafrika, 1450
        • Investigational Site Number 710917
      • Bloemfontein, Sydafrika, 9301
        • Investigational Site Number 710909
      • Bloemfontein, Sydafrika, 9301
        • Investigational Site Number 710914
      • Cape Town, Sydafrika, 7500
        • Investigational Site Number 710905
      • Cape Town, Sydafrika, 7925
        • Investigational Site Number 710904
      • Middelburg, Sydafrika, 1055
        • Investigational Site Number 710918
      • Pretoria, Sydafrika, 0002
        • Investigational Site Number 710913
      • Somerset West, Sydafrika, 7130
        • Investigational Site Number 710915
  • Ukraine
      • Kiev, Ukraine, 02091
        • Investigational Site Number 804905
      • Uzhhorod, Ukraine, 88009
        • Investigational Site Number 804902
  • Ungarn
      • Budapest, Ungarn, 1036
        • Investigational Site Number 348908
      • Budapest, Ungarn, 1134
        • Investigational Site Number 348901
      • Budapest, Ungarn, 1134
        • Investigational Site Number 348903
      • Debrecen, Ungarn, 4032
        • Investigational Site Number 348905
      • Szekesfehervar, Ungarn, 8000
        • Investigational Site Number 348906

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion criteria:

Participants with hypercholesterolemia and established coronary heart disease (CHD) or CHD risk equivalents who were not adequately controlled with a maximally tolerated daily dose of statin at stable dose for at least 4 weeks prior to the screening visit (Week -2).

Exclusion criteria:

  • Age < 18 or legal age of adulthood, whichever was greater
  • Participants without established CHD or CHD risk equivalents
  • LDL-C <70 mg/dL (<1.81 mmol/L) and participants with a history of documented cardiovascular disease
  • LDL-C <100 mg/dL (<2.59 mmol/L) and participants without a history of documented CV disease
  • Fasting serum triglycerides >400 mg/dL (>4.52 mmol/L)

The above information was not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Alirocumab 75 /up to 150 mg Q2W
Alirocumab 75 mg every 2 weeks (Q2W) and oral placebo capsule for ezetimibe daily added to stable Lipid Modifying Therapy (LMT) for 104 weeks. Alirocumab dose up-titrated to 150 mg from Week 12 when LDL-C level ≥70 mg/dL (1.81 mmol/L) at Week 8.
Medicin: Alirocumab
1 mL subkutan injektion i maven, låret eller det ydre område af overarmen ved selvinjektion eller af en anden udpeget person, der bruger autoinjektoren.
Andre navne:
  • Praluent
  • REGN727/SAR236553
Medicin: Placebo (for ezetimibe)
One capsule once daily orally at approximately the same time of the day with or without food.
Medicin: Lipid Modifying Therapy (LMT)
Statin (rosuvastatin, simvastatin or atorvastatin) at stable dose.
Aktiv komparator: Ezetimibe 10 mg
Ezetimibe 10 mg capsule daily and subcutaneous placebo for alirocumab Q2W added to stable LMT for 104 weeks.
Medicin: Ezetimibe
Én overindkapslet tablet oralt én gang dagligt på omtrent samme tidspunkt på dagen med eller uden mad.
Medicin: Lipid Modifying Therapy (LMT)
Statin (rosuvastatin, simvastatin or atorvastatin) at stable dose.
Medicin: Placebo (for alirocumab)
1 mL subcutaneous injection in the abdomen, thigh, or outer area of the upper arm by self-injection or by another designated person using the autoinjector.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Percent Change From Baseline in Calculated LDL-C at Week 24 - Intent-to-treat (ITT) Analysis
Tidsramme: From Baseline to Week 52
Adjusted Least-squares (LS) means and standard errors at Week 24 were obtained from a mixed-effect model with repeated measures (MMRM) to account for missing data. All available post-baseline data from week 4 to week 52 regardless of status on- or off-treatment were used in the model (ITT analysis).
From Baseline to Week 52

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Procentvis ændring fra baseline i ikke-højdensitetslipoproteinkolesterol (ikke-HDL-C) i uge 24 - ITT-analyse
Tidsramme: Fra baseline til uge 52
Justerede LS-middelværdier og standardfejl i uge 24 fra MMRM-modellen inklusive alle tilgængelige post-baseline-data fra uge 4 til uge 52 uanset status til- eller slukket for behandling.
Fra baseline til uge 52
Procentvis ændring fra baseline i totalt kolesterol (Total-C) i uge 24 - ITT-analyse
Tidsramme: Fra baseline til uge 52
Justerede LS-middelværdier og standardfejl i uge 24 fra MMRM-modellen inklusive alle tilgængelige post-baseline-data fra uge 4 til uge 52 uanset status til- eller slukket for behandling.
Fra baseline til uge 52
Procent ændring fra baseline i ikke-HDL-C i uge 12 - ITT-analyse
Tidsramme: Fra baseline til uge 52
Justerede LS-middelværdier og standardfejl i uge 12 fra MMRM-modellen inklusive alle tilgængelige post-baseline-data fra uge 4 til uge 52 uanset status til eller uden behandling.
Fra baseline til uge 52
Procent ændring fra baseline i Total-C i uge 12 - ITT-analyse
Tidsramme: Fra baseline til uge 52
Justerede LS-middelværdier og standardfejl i uge 12 fra MMRM-modellen inklusive alle tilgængelige post-baseline-data fra uge 4 til uge 52 uanset status til eller uden behandling.
Fra baseline til uge 52
Procent ændring fra baseline i HDL-C i uge 24 - ITT-analyse
Tidsramme: Fra baseline til uge 52
Justerede LS-middelværdier og standardfejl i uge 24 fra MMRM-modellen inklusive alle tilgængelige post-baseline-data fra uge 4 til uge 52 uanset status til- eller slukket for behandling.
Fra baseline til uge 52
Procent ændring fra baseline i HDL-C i uge 12 - ITT-analyse
Tidsramme: Fra baseline til uge 52
Justerede LS-middelværdier og standardfejl i uge 12 fra MMRM-modellen inklusive alle tilgængelige post-baseline-data fra uge 4 til uge 52 uanset status til eller uden behandling.
Fra baseline til uge 52
Procent ændring fra baseline i Lipoprotein(a) i uge 24 - ITT-analyse
Tidsramme: Fra baseline til uge 52
Justerede gennemsnit og standardfejl i uge 24 blev opnået fra multiple imputationstilgang efterfulgt af robust regressionsmodel til håndtering af manglende data. Alle tilgængelige post-baseline-data fra uge 4 til uge 52 uanset status til- eller uden behandling blev inkluderet i imputationsmodellen.
Fra baseline til uge 52
Procent ændring fra baseline i Apo A-1 i uge 12 - ITT-analyse
Tidsramme: Fra baseline til uge 52
Justerede LS-middelværdier og standardfejl i uge 12 fra MMRM-modellen inklusive alle tilgængelige post-baseline-data fra uge 4 til uge 52 uanset status til- eller slukket for behandling.
Fra baseline til uge 52
Percent Change From Baseline in Fasting Triglycerides at Week 24 - ITT Analysis
Tidsramme: From Baseline to Week 52
Adjusted means and standard errors at Week 24 from multiple imputation approach followed by robust regression model including all available post-baseline data from Week 4 to Week 52 regardless of status on- or off-treatment.
From Baseline to Week 52
Percent Change From Baseline in Apolipoprotein A-1 (Apo A-1) at Week 24 - ITT Analysis
Tidsramme: From Baseline to Week 52
Adjusted LS means and standard errors at Week 24 from MMRM model including all available post-baseline data from Week 4 to Week 52 regardless of status on- or off-treatment.
From Baseline to Week 52
Percent Change From Baseline in Fasting Triglycerides at Week 12 - ITT Analysis
Tidsramme: From Baseline to Week 52
Adjusted means and standard errors at Week 12 from multiple imputation approach followed by robust regression model including all available post-baseline data from Week 4 to Week 52 regardless of status on- or off-treatment.
From Baseline to Week 52
Percent Change From Baseline in Calculated LDL--C at Week 24 - On--Treatment Analysis
Tidsramme: From Baseline to Week 52
Adjusted LS means and standard errors at Week 24 were obtained from MMRM model including available post-baseline on-treatment data from Week 4 to Week 52 (i.e. up to 21 days after last injection or 3 days after the last capsule, whichever came first).
From Baseline to Week 52
Percent Change From Baseline in Calculated LDL-C at Week 12 - ITT Analysis
Tidsramme: From Baseline to Week 52
Adjusted LS means and standard errors at Week 12 from a MMRM including all available post-baseline data from week 4 to week 52 regardless of status on- or off-treatment.
From Baseline to Week 52
Percent Change From Baseline in Calculated LDL-C at Week 12 - On-Treatment Analysis
Tidsramme: From Baseline to Week 52
Adjusted LS means and standard errors at Week 12 from MMRM model including available post-baseline on-treatment data from Week 4 to Week 52 (i.e. up to 21 days after last injection or 3 days after the last capsule, whichever came first).
From Baseline to Week 52
Percent Change From Baseline in Apolipoprotein B (Apo-B) at Week 24 - ITT Analysis
Tidsramme: From Baseline to Week 52
Adjusted LS means and standard errors at Week 24 from MMRM model including all available post-baseline data from Week 4 to Week 52 regardless of status on- or off-treatment.
From Baseline to Week 52
Percent Change From Baseline in Apo B at Week 24 - On-Treatment Analysis
Tidsramme: From Baseline to Week 52
Adjusted LS means and standard errors at Week 24 from MMRM model including available post-baseline on-treatment data from Week 4 to Week 52 (i.e. up to 21 days after last injection or 3 days after the last capsule, whichever came first).
From Baseline to Week 52
Percent Change From Baseline in Non-HDL-C at Week 24 - On-Treatment Analysis
Tidsramme: From Baseline up to Week 52
Adjusted LS means and standard errors at Week 24 from MMRM model including available post-baseline on-treatment data from Week 4 to Week 52 (i.e. up to 21 days after last injection or 3 days after the last capsule, whichever came first).
From Baseline up to Week 52
Percent Change From Baseline in Apo-B at Week 12 - ITT Analysis
Tidsramme: From Baseline to Week 52
Adjusted LS means and standard errors at Week 12 from MMRM model including all available post-baseline data from Week 4 to Week 52 regardless of status on- or off-treatment.
From Baseline to Week 52
Percent Change From Baseline in Calculated LDL-C at Week 52 - ITT Analysis
Tidsramme: From Baseline to Week 52
Adjusted LS means and standard errors at Week 52 from a MMRM model including all available post-baseline data from week 4 to week 52 regardless of status on- or off-treatment.
From Baseline to Week 52
Percentage of Participants Achieving Calculated LDL-C <70 mg/dL (1.81 mmol/L) at Week 24 - ITT Analysis
Tidsramme: Up to Week 52
Adjusted percentages at Week 24 were obtained from multiple imputation approach for handling of missing data. All available post-baseline data from week 4 to week 52 regardless of status on- or off-treatment were included in the imputation model.
Up to Week 52
Percentage of Participants Achieving Calculated LDL-C <70 mg/dL (1.81 mmol/L) at Week 24 - On-Treatment Analysis
Tidsramme: Up to Week 52
Adjusted percentages at Week 24 from multiple imputation approach including available post-baseline on-treatment data from week 4 to week 52 (i.e. up to 21 days after last injection or 3 days after the last capsule, whichever came first).
Up to Week 52
Percent Change From Baseline in Lipoprotein(a) at Week 12 - ITT Analysis
Tidsramme: From Baseline to Week 52
Adjusted means and standard errors at Week 12 from multiple imputation approach followed by robust regression model including all available post-baseline data from Week 4 to Week 52 regardless of status on- or off-treatment.
From Baseline to Week 52

Andre resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Percent Change From Baseline in Calculated LDL-C at Week 52 - On-Treatment Analysis
Tidsramme: From Baseline to Week 52
Adjusted LS means and standard errors at Week 52 from MMRM model including available post-baseline on-treatment data from Week 4 to Week 52 (i.e. up to 21 days after last injection or 3 days after the last capsule, whichever came first).
From Baseline to Week 52
Percent Change From Baseline in Calculated LDL-C at Week 104 - ITT Analysis
Tidsramme: From Baseline to Week 104
Adjusted LS means and standard errors at Week 104 from MMRM including all available post-baseline data from Week 4 to Week 104 regardless of status on-or off-treatment.
From Baseline to Week 104
Percent Change From Baseline in Calculated LDL-C at Week 104 - On-Treatment Analysis
Tidsramme: From Baseline to Week 104
Adjusted LS means and standard errors at Week 104 from MMRM model including available post-baseline on-treatment data from Week 4 to Week 104 (i.e. up to 21 days after last injection or 3 days after the last capsule, whichever came first).
From Baseline to Week 104

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Sanofi

Samarbejdspartnere

Regeneron Pharmaceuticals

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. august 2012

Primær færdiggørelse (Faktiske)

1. maj 2014

Studieafslutning (Faktiske)

1. juli 2015

Datoer for studieregistrering

Først indsendt

16. juli 2012

Først indsendt, der opfyldte QC-kriterier

16. juli 2012

Først opslået (Skøn)

18. juli 2012

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

4. august 2016

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

23. juni 2016

Sidst verificeret

1. juni 2016

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • EFC11569
  • U1111-1121-4315 (Anden identifikator: UTN)
  • 2011-004130-34 (EudraCT nummer)

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