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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01147250
Other study ID # EFC11319
Secondary ID 2009-012852-26U1
Status Completed
Phase Phase 3
First received June 17, 2010
Last updated February 16, 2016
Start date June 2010
Est. completion date February 2015

Study information

Verified date February 2016
Source Sanofi
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Primary Objective:

- To demonstrate that lixisenatide can reduce cardiovascular morbidity and mortality [composite endpoint of cardiovascular (CV) death, non-fatal myocardial infarction (MI), non-fatal stroke, hospitalization for unstable angina] compared to placebo in type 2 diabetic patients who recently experienced an acute coronary syndrome (ACS) event.

Secondary Objectives:

To demonstrate that when compared to placebo, lixisenatide can reduce:

- composite endpoint of cardiovascular death, non-fatal MI, non-fatal stroke, hospitalization for unstable angina, or hospitalization for heart failure

- composite endpoint of cardiovascular death, non-fatal MI, non-fatal stroke, hospitalization for unstable angina, hospitalization for heart failure, or coronary revascularization procedure

- urinary albumin excretion (based on the urinary albumin/creatinine ratio).

To assess the safety and tolerability of lixisenatide.


Description:

The estimated maximum study duration for the first randomized patient will be approximately 204 weeks (± 14 days), with a median follow-up over all patients of approximately 91 weeks, broken down as follows:

- placebo-run-in period: 7 days (+ 3 days)

- double-blind study treatment period: 203 weeks (± 14 days) (with about a 37 months of recruitment period)

- post-treatment follow-up period: 3 days (± 1 day)

All patients will be followed from randomization until the end of study, which should occur when the last randomized patient has been followed for approximately 10 months. The actual end date of the study will be "event driven"and the study will end when there are approximately 844 positively-adjudicated primary cardiovascular outcome events.


Recruitment information / eligibility

Status Completed
Enrollment 6076
Est. completion date February 2015
Est. primary completion date February 2015
Accepts healthy volunteers No
Gender Both
Age group 30 Years and older
Eligibility Inclusion criteria:

- Men and women who experienced a spontaneous acute coronary syndrome (ACS) event [i.e., ST-segment elevation myocardial infarction (STEMI)] or non-ST-segment elevation myocardial infarction (NSTEMI) or unstable angina (USA)] with a documented elevation above the normal reference range of a cardiac biomarker (Troponin or Creatinine Kinase (CK)-MB) and the clinical presentation consistent with an acute coronary syndrome which leads to admission to an acute care facility, within 180 days following the ACS event and prior to screening.

- Patients with a history of type 2 diabetes (for patients newly diagnosed, diagnosis will be based on the World Health Organization (WHO) criteria: i.e., either a fasting venous plasma glucose concentration = 7.0 mmol/L [126 mg/dL] or 2-hour post glucose load venous plasma glucose = 11.1 mmol/L [200 mg/dL], confirmed on 2 occasions) prior to the screening visit.

Exclusion criteria:

- Type 1 diabetes mellitus or history of ketoacidosis within 6 months prior to screening.

- HbA1c <5.5 % or >11% measured at screening visit.

- Required to use incretin-based agents (eg, Glucagon-like peptide -1(GLP-1) agonists or Dipeptidyl Peptidase-4 (DPP-4) inhibitors) other than the study drug during the doubleblind treatment period.

- Patients who have undergone CABG surgery following the qualifying ACS event.

- Patients who have undergone PCI within 15 days prior to screening.

- Patients with planned revascularization procedure (PCI or CABG) or coronary angiogram within 90 days after screening visit.

- History of unexplained pancreatitis, chronic pancreatitis, pancreatectomy, stomach/gastric surgery, inflammatory bowel disease, personal or family history of medullary thyroid cancer (MTC), or genetic conditions that predisposes to MTC (eg, multiple endocrine neoplasia syndromes).

- Any clinically significant abnormality identified at the time of screening that in the judgment of the Investigator or any sub-Investigator would preclude safe completion of the study or constrain endpoints assessment such as major systemic diseases.

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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
lixisenatide (AVE0010)
Pharmaceutical form:sterile aqueous solution Route of administration: subcutaneous
placebo
Pharmaceutical form:sterile aqueous solution Route of administration: subcutaneous

Locations

Country Name City State
Argentina Investigational Site Number 032028 Adrogue
Argentina Investigational Site Number 032030 Bahia Blanca
Argentina Investigational Site Number 032043 Bahia Blanca
Argentina Investigational Site Number 032054 Bahia Blanca
Argentina Investigational Site Number 032003 Caba
Argentina Investigational Site Number 032049 Caba
Argentina Investigational Site Number 032056 Caba
Argentina Investigational Site Number 032066 Caba
Argentina Investigational Site Number 032009 Capital Federal
Argentina Investigational Site Number 032017 Capital Federal
Argentina Investigational Site Number 032050 Cipolletti
Argentina Investigational Site Number 032052 Ciudad Autonoma De Bs.As
Argentina Investigational Site Number 032011 Cordoba
Argentina Investigational Site Number 032022 Cordoba
Argentina Investigational Site Number 032037 Cordoba
Argentina Investigational Site Number 032015 Córdoba
Argentina Investigational Site Number 032020 Coronel Suarez
Argentina Investigational Site Number 032004 Corrientes
Argentina Investigational Site Number 032018 Corrientes
Argentina Investigational Site Number 032005 Godoy Cruz
Argentina Investigational Site Number 032042 Haedo
Argentina Investigational Site Number 032019 Junin
Argentina Investigational Site Number 032063 La Plata
Argentina Investigational Site Number 032040 Lanus
Argentina Investigational Site Number 032036 Mar Del Plata
Argentina Investigational Site Number 032039 Mar Del Plata
Argentina Investigational Site Number 032058 Mendoza
Argentina Investigational Site Number 032038 Moron
Argentina Investigational Site Number 032002 Parana
Argentina Investigational Site Number 032023 Qilmes
Argentina Investigational Site Number 032047 Rafaela
Argentina Investigational Site Number 032024 Ramos Mejia
Argentina Investigational Site Number 032006 Resistencia
Argentina Investigational Site Number 032012 Rosario
Argentina Investigational Site Number 032027 Rosario
Argentina Investigational Site Number 032055 Salta
Argentina Investigational Site Number 032065 Salta
Argentina Investigational Site Number 032008 San Miguel De Tucuman
Argentina Investigational Site Number 032051 San Miguel De Tucuman
Argentina Investigational Site Number 032033 San Nicolas
Argentina Investigational Site Number 032035 Santa Fe
Argentina Investigational Site Number 032045 Santa Fe
Argentina Investigational Site Number 032062 Santa Rosa
Argentina Investigational Site Number 032034 Venado Tuerto
Argentina Investigational Site Number 032046 Villa Maria
Argentina Investigational Site Number 032029 Zarate
Australia Investigational Site Number 036015 Epping
Australia Investigational Site Number 036001 Fremantle
Australia Investigational Site Number 036009 Geelong
Australia Investigational Site Number 036011 Perth
Australia Investigational Site Number 036005 St Leonards
Australia Investigational Site Number 036016 Townsville
Austria Investigational Site Number 040002 Graz
Austria Investigational Site Number 040001 Wien
Belarus Investigational Site Number 112001 Minsk
Belarus Investigational Site Number 112002 Minsk
Belarus Investigational Site Number 112003 Minsk
Belgium Investigational Site Number 056001 Bruxelles
Belgium Investigational Site Number 056003 Leuven
Brazil Investigational Site Number 076024 Belem
Brazil Investigational Site Number 076006 Belo Horizonte
Brazil Investigational Site Number 076012 Belo Horizonte
Brazil Investigational Site Number 076021 Brasilia
Brazil Investigational Site Number 076002 Campinas
Brazil Investigational Site Number 076019 Curitiba
Brazil Investigational Site Number 076003 Fortaleza
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Brazil Investigational Site Number 076026 Porto Alegre
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Brazil Investigational Site Number 076020 Salvador
Brazil Investigational Site Number 076001 Sao Paulo
Brazil Investigational Site Number 076005 Sao Paulo
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Brazil Investigational Site Number 076007 Uberlandia
Bulgaria Investigational Site Number 100002 Byala
Bulgaria Investigational Site Number 100011 Gabrovo
Bulgaria Investigational Site Number 100001 Kazanluk
Bulgaria Investigational Site Number 100006 Lovech
Bulgaria Investigational Site Number 100004 Pleven
Bulgaria Investigational Site Number 100003 Plovdiv
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Bulgaria Investigational Site Number 100016 Sandanski
Bulgaria Investigational Site Number 100010 Sofia
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Bulgaria Investigational Site Number 100005 Varna
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Canada Investigational Site Number 124016 Cambridge
Canada Investigational Site Number 124026 Edmonton
Canada Investigational Site Number 124001 Laval
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Canada Investigational Site Number 124021 Montreal
Canada Investigational Site Number 124027 Oshawa
Canada Investigational Site Number 124025 Quebec
Canada Investigational Site Number 124028 Red Deer
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Canada Investigational Site Number 124003 St-Marc-Des-Carrieres
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Georgia Investigational Site Number 268003 Batumi
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Germany Investigational Site Number 276003 Berlin
Germany Investigational Site Number 276022 Bochum
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Germany Investigational Site Number 276024 Dresden
Germany Investigational Site Number 276007 Elsterwerda
Germany Investigational Site Number 276018 Frankfurt A.M.
Germany Investigational Site Number 276011 Frankfurt Am Main
Germany Investigational Site Number 276017 Görlitz
Germany Investigational Site Number 276025 Haßloch
Germany Investigational Site Number 276009 Heidelberg
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Germany Investigational Site Number 276020 Magdeburg
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Guatemala Investigational Site Number 320001 Guatemala
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Guatemala Investigational Site Number 320011 Guatemala
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Japan Investigational Site Number 392011 Chuo-Ku
Japan Investigational Site Number 392015 Fuchu-Shi
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Japan Investigational Site Number 392027 Hakusan-Shi
Japan Investigational Site Number 392005 Hamamatsu-Shi
Japan Investigational Site Number 392022 Hitachi-Shi
Japan Investigational Site Number 392003 Itabashi-Ku
Japan Investigational Site Number 392017 Itabashi-Ku
Japan Investigational Site Number 392019 Kawanishi-Shi
Japan Investigational Site Number 392013 Kobe-Shi
Japan Investigational Site Number 392007 Matsuyama-Shi
Japan Investigational Site Number 392008 Matsuyama-Shi
Japan Investigational Site Number 392009 Nagasaki-Shi
Japan Investigational Site Number 392002 Noda-Shi
Japan Investigational Site Number 392020 Osaka-Shi
Japan Investigational Site Number 392021 Osaka-Shi
Japan Investigational Site Number 392001 Sapporo-Shi
Japan Investigational Site Number 392010 Sapporo-Shi
Japan Investigational Site Number 392024 Setagaya-Ku
Japan Investigational Site Number 392004 Shinagawa-Ku
Japan Investigational Site Number 392014 Shirakawa-Shi
Japan Investigational Site Number 392018 Suita-Shi
Japan Investigational Site Number 392016 Tachikawa-Shi
Japan Investigational Site Number 392023 Takasaki-Shi
Korea, Republic of Investigational Site Number 410012 Bucheon
Korea, Republic of Investigational Site Number 410006 Daegu
Korea, Republic of Investigational Site Number 410009 Gwangju
Korea, Republic of Investigational Site Number 410001 Incheon
Korea, Republic of Investigational Site Number 410008 Incheon
Korea, Republic of Investigational Site Number 410004 Seongnam
Korea, Republic of Investigational Site Number 410002 Seoul
Korea, Republic of Investigational Site Number 410010 Seoul
Korea, Republic of Investigational Site Number 410011 Seoul
Korea, Republic of Investigational Site Number 410013 Seoul
Korea, Republic of Investigational Site Number 410014 Seoul
Korea, Republic of Investigational Site Number 410007 Wonju
Latvia Investigational Site Number 428005 Cesis
Latvia Investigational Site Number 428001 Daugavpils
Latvia Investigational Site Number 428002 Liepaja
Latvia Investigational Site Number 428003 Riga
Latvia Investigational Site Number 428004 Riga
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Lithuania Investigational Site Number 440002 Kaunas
Lithuania Investigational Site Number 440003 Kaunas
Lithuania Investigational Site Number 440004 Klaipeda
Lithuania Investigational Site Number 440006 Klaipeda
Lithuania Investigational Site Number 440005 Panevezys
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Mexico Investigational Site Number 484011 Acapulco
Mexico Investigational Site Number 484008 Aguascalientes
Mexico Investigational Site Number 484033 Aguascalientes
Mexico Investigational Site Number 484016 Chihuahua
Mexico Investigational Site Number 484023 Ciudad Madero
Mexico Investigational Site Number 484001 Durango
Mexico Investigational Site Number 484007 Durango
Mexico Investigational Site Number 484041 Durango
Mexico Investigational Site Number 484006 Guadalajara
Mexico Investigational Site Number 484014 Guadalajara
Mexico Investigational Site Number 484018 Guadalajara
Mexico Investigational Site Number 484021 Guadalajara
Mexico Investigational Site Number 484028 Guadalajara
Mexico Investigational Site Number 484032 Guadalajara
Mexico Investigational Site Number 484034 Guadalajara
Mexico Investigational Site Number 484024 Leon
Mexico Investigational Site Number 484013 Mexico City
Mexico Investigational Site Number 484022 Mexico City
Mexico Investigational Site Number 484026 Mexico City
Mexico Investigational Site Number 484002 Monterrey
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Mexico Investigational Site Number 484035 Morelia
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Netherlands Investigational Site Number 528005 Alkmaar
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Norway Investigational Site Number 578003 Bodø
Norway Investigational Site Number 578002 Haugesund
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Panama Investigational Site Number 591001 Cuidad De Panama
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Peru Investigational Site Number 604007 Arequipa
Peru Investigational Site Number 604014 Callao
Peru Investigational Site Number 604001 Lima
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Peru Investigational Site Number 604006 Lima
Peru Investigational Site Number 604009 Lima
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Philippines Investigational Site Number 608006 Cavite
Philippines Investigational Site Number 608009 Iligan City, Lanao Del Norte
Philippines Investigational Site Number 608003 Makati City
Philippines Investigational Site Number 608001 Manila
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Philippines Investigational Site Number 608005 Marikina City
Philippines Investigational Site Number 608002 Pasay City
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Poland Investigational Site Number 616005 ?ód?
Poland Investigational Site Number 616008 Bialystok
Poland Investigational Site Number 616019 Bydgoszcz
Poland Investigational Site Number 616012 Czeladz
Poland Investigational Site Number 616007 Czestochowa
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Poland Investigational Site Number 616028 Grodzisk Mazowiecki
Poland Investigational Site Number 616022 Katowice
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Portugal Investigational Site Number 620005 Amadora
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Portugal Investigational Site Number 620001 Lisboa
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Romania Investigational Site Number 642029 Arad
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Romania Investigational Site Number 642034 Bucharest
Romania Investigational Site Number 642001 Bucuresti
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Romania Investigational Site Number 642022 Bucuresti
Romania Investigational Site Number 642026 Cluj Napoca
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Romania Investigational Site Number 642018 Timisoara
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Russian Federation Investigational Site Number 643023 Barnaul
Russian Federation Investigational Site Number 643044 Kazan
Russian Federation Investigational Site Number 643005 Kemerovo
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Russian Federation Investigational Site Number 643027 Krasnodar
Russian Federation Investigational Site Number 643061 Krasnodar
Russian Federation Investigational Site Number 643001 Moscow
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Russian Federation Investigational Site Number 643003 Moscow
Russian Federation Investigational Site Number 643008 Moscow
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Russian Federation Investigational Site Number 643026 Moscow
Russian Federation Investigational Site Number 643029 Moscow
Russian Federation Investigational Site Number 643037 Moscow
Russian Federation Investigational Site Number 643038 Moscow
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Russian Federation Investigational Site Number 643042 Moscow
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Russian Federation Investigational Site Number 643051 Moscow
Russian Federation Investigational Site Number 643052 Moscow
Russian Federation Investigational Site Number 643060 Moscow
Russian Federation Investigational Site Number 643034 Nizhny Novgorod
Russian Federation Investigational Site Number 643054 Novosibirsk
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Russian Federation Investigational Site Number 643045 Omsk
Russian Federation Investigational Site Number 643030 Penza
Russian Federation Investigational Site Number 643017 Perm
Russian Federation Investigational Site Number 643049 Perm
Russian Federation Investigational Site Number 643048 Rostov-Na-Donu
Russian Federation Investigational Site Number 643047 Ryazan
Russian Federation Investigational Site Number 643039 Saint-Petersburg
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Russian Federation Investigational Site Number 643025 Saratov
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Sponsors (1)

Lead Sponsor Collaborator
Sanofi

Countries where clinical trial is conducted

United States,  Argentina,  Australia,  Austria,  Belarus,  Belgium,  Brazil,  Bulgaria,  Canada,  Chile,  China,  Colombia,  Denmark,  Ecuador,  Egypt,  Estonia,  Finland,  France,  Georgia,  Germany,  Guatemala,  India,  Israel,  Italy,  Japan,  Korea, Republic of,  Latvia,  Lithuania,  Mexico,  Netherlands,  Norway,  Panama,  Peru,  Philippines,  Poland,  Portugal,  Romania,  Russian Federation,  Serbia,  South Africa,  Spain,  Sweden,  Switzerland,  Taiwan,  Tunisia,  Turkey,  Ukraine,  United Arab Emirates,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time to the first occurrence of the primary cardiovascular (CV) event: CV death, non-fatal MI, non-fatal stroke, hospitalization for unstable angina, positively adjudicated by the Cardiovascular Events Adjudication Committee (CAC) week 0 to week 203 No
Secondary Time to the first occurrence of cardiovascular (CV) death, non-fatal MI, non-fatal stroke, hospitalization for unstable angina, hospitalization for heart failure positively adjudicated by the CAC week 0 to week 203 No
Secondary Time to the first occurrence of cardiovascular (CV) death, non-fatal MI, non-fatal stroke, hospitalization for unstable angina, hospitalization for heart failure, coronary revascularization procedure positively adjudicated by the CAC week 0 to week 203 No
Secondary Percent change in the urinary albumin/creatinine ratio From baseline to 108 weeks No
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