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    The EU Clinical Trials Register currently displays   43857   clinical trials with a EudraCT protocol, of which   7284   are clinical trials conducted with subjects less than 18 years old.   The register also displays information on   18700   older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).

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    Summary
    EudraCT Number:2011-000997-77
    Sponsor's Protocol Code Number:GS-US-259-0110
    National Competent Authority:Poland - Office for Medicinal Products
    Clinical Trial Type:EEA CTA
    Trial Status:Completed
    Date on which this record was first entered in the EudraCT database:2012-02-03
    Trial results View results
    Index
    A. PROTOCOL INFORMATION
    B. SPONSOR INFORMATION
    C. APPLICANT IDENTIFICATION
    D. IMP IDENTIFICATION
    D.8 INFORMATION ON PLACEBO
    E. GENERAL INFORMATION ON THE TRIAL
    F. POPULATION OF TRIAL SUBJECTS
    G. INVESTIGATOR NETWORKS TO BE INVOLVED IN THE TRIAL
    N. REVIEW BY THE COMPETENT AUTHORITY OR ETHICS COMMITTEE IN THE COUNTRY CONCERNED
    P. END OF TRIAL
    Expand All   Collapse All
    A. Protocol Information
    A.1Member State ConcernedPoland - Office for Medicinal Products
    A.2EudraCT number2011-000997-77
    A.3Full title of the trial
    A Phase 3, Randomized, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Efficacy and Safety of Ranolazine When Added to Glimepiride in Subjects with Type 2 Diabetes Mellitus
    A.3.1Title of the trial for lay people, in easily understood, i.e. non-technical, language
    A study to investigate a new drug to treat Type 2 Diabetes
    A.4.1Sponsor's protocol code numberGS-US-259-0110
    A.7Trial is part of a Paediatric Investigation Plan No
    A.8EMA Decision number of Paediatric Investigation Plan
    B. Sponsor Information
    B.Sponsor: 1
    B.1.1Name of SponsorGilead Sciences, Inc.
    B.1.3.4CountryUnited States
    B.3.1 and B.3.2Status of the sponsorCommercial
    B.4 Source(s) of Monetary or Material Support for the clinical trial:
    B.4.1Name of organisation providing supportGilead Sciences, Inc.
    B.4.2CountryUnited States
    B.5 Contact point designated by the sponsor for further information on the trial
    B.5.1Name of organisationGilead Sciences International Ltd
    B.5.2Functional name of contact pointInternational Regulatory Affairs
    B.5.3 Address:
    B.5.3.1Street AddressFlowers Building, Granta Park
    B.5.3.2Town/ cityAbington
    B.5.3.3Post codeCB21 6GT
    B.5.3.4CountryUnited Kingdom
    B.5.4Telephone number+442085872210
    B.5.5Fax number+441223897284
    B.5.6E-mailclinical.trials@gilead.com
    D. IMP Identification
    D.IMP: 1
    D.1.2 and D.1.3IMP RoleTest
    D.2 Status of the IMP to be used in the clinical trial
    D.2.1IMP to be used in the trial has a marketing authorisation Yes
    D.2.1.1.1Trade name Ranexa®
    D.2.1.1.2Name of the Marketing Authorisation holderMenarini International Operations Luxembourg S.A
    D.2.1.2Country which granted the Marketing AuthorisationEuropean Union
    D.2.5The IMP has been designated in this indication as an orphan drug in the Community No
    D.2.5.1Orphan drug designation number
    D.3 Description of the IMP
    D.3.4Pharmaceutical form Prolonged-release tablet
    D.3.4.1Specific paediatric formulation No
    D.3.7Routes of administration for this IMPOral use
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNRANOLAZINE
    D.3.9.1CAS number 95635-55-5
    D.3.9.4EV Substance CodeSUB10259MIG
    D.3.10 Strength
    D.3.10.1Concentration unit mg milligram(s)
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number500
    D.3.11 The IMP contains an:
    D.3.11.1Active substance of chemical origin Yes
    D.3.11.2Active substance of biological/ biotechnological origin (other than Advanced Therapy IMP (ATIMP) No
    The IMP is a:
    D.3.11.3Advanced Therapy IMP (ATIMP) No
    D.3.11.3.1Somatic cell therapy medicinal product No
    D.3.11.3.2Gene therapy medical product No
    D.3.11.3.3Tissue Engineered Product No
    D.3.11.3.4Combination ATIMP (i.e. one involving a medical device) No
    D.3.11.3.5Committee on Advanced therapies (CAT) has issued a classification for this product No
    D.3.11.4Combination product that includes a device, but does not involve an Advanced Therapy No
    D.3.11.5Radiopharmaceutical medicinal product No
    D.3.11.6Immunological medicinal product (such as vaccine, allergen, immune serum) No
    D.3.11.7Plasma derived medicinal product No
    D.3.11.8Extractive medicinal product No
    D.3.11.9Recombinant medicinal product No
    D.3.11.10Medicinal product containing genetically modified organisms No
    D.3.11.11Herbal medicinal product No
    D.3.11.12Homeopathic medicinal product No
    D.3.11.13Another type of medicinal product No
    D.8 Information on Placebo
    D.8 Placebo: 1
    D.8.1Is a Placebo used in this Trial?Yes
    D.8.3Pharmaceutical form of the placeboFilm-coated tablet
    D.8.4Route of administration of the placeboOral use
    E. General Information on the Trial
    E.1 Medical condition or disease under investigation
    E.1.1Medical condition(s) being investigated
    Type 2 Diabetes Mellitus
    E.1.1.1Medical condition in easily understood language
    Diabetes
    E.1.1.2Therapeutic area Diseases [C] - Nutritional and Metabolic Diseases [C18]
    MedDRA Classification
    E.1.2 Medical condition or disease under investigation
    E.1.2Version 16.0
    E.1.2Level PT
    E.1.2Classification code 10067585
    E.1.2Term Type 2 diabetes mellitus
    E.1.2System Organ Class 10027433 - Metabolism and nutrition disorders
    E.1.3Condition being studied is a rare disease No
    E.2 Objective of the trial
    E.2.1Main objective of the trial
    The primary objective of the study is to:
    • Determine the effect of ranolazine on hemoglobin A1c
    (HbA1c) after 24 weeks of treatment when added to
    glimepiride in subjects who have inadequately controlled type
    2 diabetes mellitus (T2DM) despite current treatment with
    stable sulfonylurea (SU) or metformin therapy in addition to
    diet and exercise
    E.2.2Secondary objectives of the trial
    The secondary objectives of the study are to:
    • Determine the effect of ranolazine when added to glimepiride
    on postprandial serum glucose (PPG)
    • Determine the effect of ranolazine when added to glimepiride
    on fasting serum glucose (FSG)

    The additional objectives of the study are to:
    • Evaluate the effect of ranolazine when added to glimepiride on
    each of the following parameters: serum C-peptide, serum
    insulin, and plasma glucagon
    • Evaluate the pharmacokinetics (PK) of ranolazine

    The safety objective of the study is to:
    • Evaluate the safety and tolerability of ranolazine when added to
    glimepiride in subjects who have inadequately controlled
    T2DM despite current treatment with stable SU or metformin
    therapy in addition to diet and exercise
    E.2.3Trial contains a sub-study No
    E.3Principal inclusion criteria
    1. Written informed consent

    2. Males and females, 18 to 75 years old, inclusive

    3. Documented history of T2DM

    4. Receiving one of the following SU or metformin therapies in addition to diet and exercise for at least 90 days prior to Screening:
    a. glimepiride at a daily dose of ≥ 2 mg and ≤ 4 mg
    b. glipizide, glyburide, or glibenclamide (or equivalent) at a daily dose of ≥ 7.5 mg
    c. gliclazide at a daily dose of > 160 mg (or ≥ 60 mg for the MR formulation)
    d. metformin at a daily dose of ≥ 1500 mg

    5. Body mass index (BMI) 25 kg/m2 to 45 kg/m2, inclusive, at Screening

    6. HbA1c 7% to 10%, inclusive, at Screening and the end of the Qualifying Period (Day 14 + 2 days)

    7. Fasting serum C-peptide ≥ 0.8 ng/mL at Screening

    8. FSG ≥ 130 mg/dL (7.2 mmol/L) and ≤ 240 mg/dL (13.3 mmol/L) at
    Screening and at the end of the Qualifying Period (Day 14 + 2 days):A
    one-time central laboratory re-test of FSG is allowed in subjects with an
    initial central laboratory FSG ≥ 120 mg/dL (6.7mmol/L) and <130
    mg/dL (7.2 mmol/L) who are otherwise eligible as determined by the
    investigator.

    9. Able and willing to comply with all study procedures during the course of the study

    10. Females of child-bearing potential must have a negative serum pregnancy test at Screening and must agree to use highly effective contraception methods from Screening throughout the duration of
    the Treatment Period and for 14 days following the last dose of study drug

    11. At least 80% compliant in dosing during the Qualifying Period
    E.4Principal exclusion criteria
    Disease-specific:
    1.History of or current diagnosis of type 1DM
    2.History of diabetic ketoacidosis,ketosis-prone diabetes, or hyperosmolar hyperglycemic coma
    3.History of a severe episode of hypoglycemia (≥1 episode within 3 months prior to Screen or ≥2 episodes within 6 months prior to Screen),defined as hypoglycemia requiring 3rd party assistance to actively administer carbohydrate, glucagon,or other resuscitative actions due to severe impairment in consciousness or behavior
    4.Clinically significant complications of diabetes that in the judgment of the investigator would make the subject unsuitable to participate in this study
    5.History of any clinically significant CV or cerebrovascular event ≤ 3 months prior to Screen
    6.Inadequately controlled or unstable hypertension as defined by SBP > 160 mmHg or DBP > 100 mmHg at Screen and at Randomization
    7.Prolonged QTc interval > 500 msec by ECG at Screen,a personal or family history of QTc prolongation,congenital long QT syndrome,or subjects who are receiving drugs that prolong the QTc interval,such as Class Ia or Class III antiarrhythmic agents, erythromycin,and certain antipsychotics (eg, ziprasidone)
    8.History of bariatric surgery at any time in the past or any other surgery <2 months before Screen;or planning to undergo surgery during the study.Subjects with a planned minor surgery may be enrolled upon approval by the Medical Monitor
    9.Any other hospitalization in the 14 days prior to Screen or planned hospitalization at any time during the study
    10.Significant weight change (± 5%) < 2 months prior to Screen or enrollment in a weight-loss program other than a maintenance phase at Screen
    11.Severe renal impairment,defined as an estimated glomerular filtration rate (eGFR) by the MDRD equation <30 mL/min/1.73 m2 at Screen or undergoing any type of dialysis at Screen or planning to undergo any type of dialysis during the course of the study
    12.History of liver cirrhosis (Child-Pugh Class A,B,or C)
    13.Active liver disease and/or significant abnormal liver function defined as AST > 3x ULN and/or ALT > 3x ULN and/or serum total bilirubin > 2.0 mg/dL
    14.History of cancer (except non-melanomic skin cancers or cervical in situ) within 5 years prior to Screen
    15.History of alcohol or other drug abuse < 12 months prior to Screen
    16.Any other clinically significant existing medical or psychiatric condition,including clinically significant laboratory abnormalities,or one requiring further evaluation that in the opinion of the investigator could interfere with conduct of the study or interpretation of the data
    17.Use of antihyperglycemic agents other than SU agents or metformin,including but not limited to dipeptidyl peptidase-4 inhibitors (eg, saxagliptin and sitagliptin),and glucagon-like peptide-mimetics (eg, exenatide or insulin) < 3 months prior to Screen".Use of TZDs (eg, rosiglitazone or pioglitazone) < 24 weeks prior to Screen.
    18.Previous history of intolerance of glimepiride (as a single-agent therapy)
    19.Prior treatment with open-label ranolazine,or known hypersensitivity or intolerance to ranolazine or any of its excipients
    20.Treatment with strong or moderate CYP3A inhibitors or P-gp inhibitors within 14 days prior to Randomization
    21.Treatment with CYP3A inducers or P-gp inducers within 14 days prior to Randomization
    22.Treatment with CYP3A4 substrates with a narrow therapeutic range (eg, cyclosporine, tacrolimus, or sirolimus) within 14 days prior to Randomization
    23.Treatment with simvastatin at a dose of >20 mg daily or lovastatin at a dose of >40 mg daily within 14 days prior to Randomization
    24.Weight loss medication or anti-obesity medication (prescription or non-prescription) <3 months prior to Screen
    25.Treatment with niacin >200 mg daily;if receiving ≤200 mg daily,should be on stable doses for ≥3 months prior to Screen
    26.Expected or current treatment with systemic corticosteroids (oral or injectable) for >14 days from Screen through the end of the Treatment Period.Topical or inhaled corticosteroid formulations are permitted at any time during the study.
    27.If receiving thyroid replacement therapy,should be on stable doses for at least 6 weeks prior to Randomization
    28.Hemoglobin <12 g/dL for males or <11g/dL for females at Screen
    29.Participation in another clinical study involving an investigational drug or device <30 days prior to Screen;participation in another clinical study involving an OHA <90 days prior to Screen
    30.Donation of blood <2 months prior to Screen or plans to donate blood while participating in the study
    31.Females who are pregnant or are breastfeeding
    32.Other condition(s) that,in the opinion of the investigator, would compromise the safety of the subject,prevent compliance with the study protocol (including the ability to comply with MMTT),or compromise the quality of the clinical study
    33.Severe renal impairment,defined as an estimated eGFR by the MDRD equation <30 mL/min/1.73m2 at Screen
    E.5 End points
    E.5.1Primary end point(s)
    The primary efficacy endpoint of this study is the following:
    • Change from Baseline in HbA1c at Week 24 of Treatment Period
    E.5.1.1Timepoint(s) of evaluation of this end point
    Week 24
    E.5.2Secondary end point(s)
    The secondary efficacy endpoints of this study are the following:
    • Change from Baseline in incremental change of 2-hour PPG at Week 24

    •Change from Baseline in FSG at Week 24 or change from Baseline in 2-
    hour PPG at Week 24
    E.5.2.1Timepoint(s) of evaluation of this end point
    Week 24
    E.6 and E.7 Scope of the trial
    E.6Scope of the trial
    E.6.1Diagnosis No
    E.6.2Prophylaxis No
    E.6.3Therapy No
    E.6.4Safety Yes
    E.6.5Efficacy Yes
    E.6.6Pharmacokinetic Yes
    E.6.7Pharmacodynamic No
    E.6.8Bioequivalence No
    E.6.9Dose response No
    E.6.10Pharmacogenetic No
    E.6.11Pharmacogenomic No
    E.6.12Pharmacoeconomic No
    E.6.13Others No
    E.7Trial type and phase
    E.7.1Human pharmacology (Phase I) No
    E.7.1.1First administration to humans No
    E.7.1.2Bioequivalence study No
    E.7.1.3Other No
    E.7.1.3.1Other trial type description
    E.7.2Therapeutic exploratory (Phase II) No
    E.7.3Therapeutic confirmatory (Phase III) Yes
    E.7.4Therapeutic use (Phase IV) No
    E.8 Design of the trial
    E.8.1Controlled Yes
    E.8.1.1Randomised Yes
    E.8.1.2Open No
    E.8.1.3Single blind No
    E.8.1.4Double blind Yes
    E.8.1.5Parallel group Yes
    E.8.1.6Cross over No
    E.8.1.7Other No
    E.8.2 Comparator of controlled trial
    E.8.2.1Other medicinal product(s) No
    E.8.2.2Placebo Yes
    E.8.2.3Other No
    E.8.2.4Number of treatment arms in the trial2
    E.8.3 The trial involves single site in the Member State concerned No
    E.8.4 The trial involves multiple sites in the Member State concerned Yes
    E.8.4.1Number of sites anticipated in Member State concerned8
    E.8.5The trial involves multiple Member States Yes
    E.8.5.1Number of sites anticipated in the EEA33
    E.8.6 Trial involving sites outside the EEA
    E.8.6.1Trial being conducted both within and outside the EEA Yes
    E.8.6.2Trial being conducted completely outside of the EEA No
    E.8.6.3If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned
    Belarus
    Czech Republic
    Hungary
    Malaysia
    Poland
    Romania
    Russian Federation
    Serbia
    Slovakia
    South Africa
    Taiwan
    Thailand
    Ukraine
    United States
    E.8.7Trial has a data monitoring committee Yes
    E.8.8 Definition of the end of the trial and justification where it is not the last visit of the last subject undergoing the trial
    Last patient last visit
    E.8.9 Initial estimate of the duration of the trial
    E.8.9.1In the Member State concerned years1
    E.8.9.1In the Member State concerned months4
    E.8.9.1In the Member State concerned days0
    E.8.9.2In all countries concerned by the trial years1
    E.8.9.2In all countries concerned by the trial months4
    E.8.9.2In all countries concerned by the trial days0
    F. Population of Trial Subjects
    F.1 Age Range
    F.1.1Trial has subjects under 18 No
    F.1.1.1In Utero No
    F.1.1.2Preterm newborn infants (up to gestational age < 37 weeks) No
    F.1.1.3Newborns (0-27 days) No
    F.1.1.4Infants and toddlers (28 days-23 months) No
    F.1.1.5Children (2-11years) No
    F.1.1.6Adolescents (12-17 years) No
    F.1.2Adults (18-64 years) Yes
    F.1.2.1Number of subjects for this age range: 300
    F.1.3Elderly (>=65 years) Yes
    F.1.3.1Number of subjects for this age range: 100
    F.2 Gender
    F.2.1Female Yes
    F.2.2Male Yes
    F.3 Group of trial subjects
    F.3.1Healthy volunteers No
    F.3.2Patients Yes
    F.3.3Specific vulnerable populations Yes
    F.3.3.1Women of childbearing potential not using contraception No
    F.3.3.2Women of child-bearing potential using contraception Yes
    F.3.3.3Pregnant women No
    F.3.3.4Nursing women No
    F.3.3.5Emergency situation No
    F.3.3.6Subjects incapable of giving consent personally No
    F.3.3.7Others No
    F.4 Planned number of subjects to be included
    F.4.1In the member state15
    F.4.2 For a multinational trial
    F.4.2.1In the EEA 33
    F.4.2.2In the whole clinical trial 400
    F.5 Plans for treatment or care after the subject has ended the participation in the trial (if it is different from the expected normal treatment of that condition)
    Long-term care for the participant will remain the responsibility of their primary treating physician
    G. Investigator Networks to be involved in the Trial
    N. Review by the Competent Authority or Ethics Committee in the country concerned
    N.Competent Authority Decision Authorised
    N.Date of Competent Authority Decision2012-04-13
    N.Ethics Committee Opinion of the trial applicationFavourable
    N.Ethics Committee Opinion: Reason(s) for unfavourable opinion
    N.Date of Ethics Committee Opinion2012-02-21
    P. End of Trial
    P.End of Trial StatusCompleted
    P.Date of the global end of the trial2013-08-29
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