MedPath

Type 2 Diabetes Evaluation of Ranolazine in Subjects With Chronic Stable Angina

Phase 4
Completed
Conditions
Angina Pectoris
Type 2 Diabetes Mellitus
Coronary Artery Disease
Interventions
Registration Number
NCT01425359
Lead Sponsor
Gilead Sciences
Brief Summary

This study will evaluate the effect of ranolazine compared to placebo on the average weekly angina frequency in subjects with chronic stable angina and coronary artery disease (CAD) who have a history of type 2 diabetes mellitus (T2DM), and whether ranolazine can reduce the frequency of angina (chest pain) attacks, compared to a placebo. Subjects will be asked to record their daily angina episodes in a diary at the end of each study day. Ranolazine is approved for the treatment of chronic angina, and is not approved for the treatment of T2DM.

Detailed Description

Participants who meet the eligibility criteria at screening will enter a 4-to 6-week Qualifying Period. The allowed concomitant antianginal medication(s) must be maintained at a stable dose throughout the study. Participants will document the number of angina episodes, number of sublingual nitroglycerin doses taken, and a dyspnea score (on a scale from 1 to 5) on a daily basis in a diary. Participants eligible to stay in the study after the Qualifying Period will enter the 8-week double-blind dosing phase. Participants will have study visits at the end of Weeks 2 and 8. Participants will continue to document the number of angina episodes and number of sublingual nitroglycerin doses taken as well as a dyspnea score on a daily basis by the end of each day in their diary. In addition, participants will be called during Week 2 and at the end of Week 5 to encourage compliance. A safety follow-up phone call will be made 14 days after the last study visit or early discontinuation.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
949
Inclusion Criteria
  • Written informed consent

  • Males and females aged at least 18 years

  • At least a 3-month history of chronic stable angina triggered by physical effort and relieved by rest and/or sublingual nitroglycerin

  • CAD documented by one or more of the following:

    1. Angiographic evidence of ≥ 50% stenosis of one or more major coronary arteries
    2. History of myocardial infarction (MI) documented by positive myocardial muscle creatine kinase (CK-MB) enzymes, troponins, or electrocardiogram (ECG) changes
    3. Cardiac imaging study or exercise test diagnostic for CAD
  • Treatment with up to 2 antianginal therapies at a stable dose for at least 2 weeks prior to the Qualifying Period.

  • Documented history of T2DM

  • Willing to maintain stable tobacco usage habits throughout the study

  • Willing to maintain stable activity levels throughout the study

  • Females of childbearing potential must agree to utilize highly effective contraception methods from Screening throughout the duration of study treatment and for 14 days following the last dose of study drug.

Exclusion Criteria
  • New York Heart Association (NYHA) Class III and IV
  • Acute coronary syndrome in the prior 2 months or planned coronary revascularization during the study period
  • Stroke or transient ischemic attack within 6 months prior to Screening
  • QTc > 500 milliseconds
  • Uncontrolled hypertension (seated systolic blood pressure > 180 mmHg or diastolic blood pressure > 110 mmHg)
  • Systolic blood pressure < 100 mmHg
  • Clinically significant hepatic impairment
  • Prior treatment with ranolazine, or known hypersensitivity or intolerance to ranolazine
  • Females who are breastfeeding
  • Positive serum pregnancy test
  • Participation in another investigational drug or device study within 1 month prior to Screening
  • Current treatment with trimetazidine, ivabradine, or nicorandil. Subjects will need to discontinue these medications 2 weeks prior to the Qualifying Period.
  • Current treatment with potent inhibitors of cytochrome (CYP)3A (eg, ketoconazole, itraconazole, clarithromycin, nefazodone, nelfinavir, ritonavir, indinavir, and saquinavir)
  • Current treatment with CYP3A and P glycoprotein (Pgp) inducers (eg, rifampicin/rifampin, carbamazepine, and St. John's wort [Hypericum perforatum])
  • Current treatment with CYP3A4 substrates with a narrow therapeutic range (eg, cyclosporine, tacrolimus, and sirolimus)
  • Subjects taking simvastatin who cannot reduce the dose to 20 mg once daily or who cannot switch to another statin
  • Current treatment with Class I or III antiarrhythmic medications
  • History of illicit drug use or alcohol abuse within 1 year of Screening
  • Any other conditions that, in the opinion of the investigator, are likely to prevent compliance with the study protocol or pose a safety concern if the subject participates in the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PlaceboRanolazine placeboQualifying phase: Participants will enter a 2-week washout period if needing to discontinue antianginal drugs (except beta-blockers) followed by placebo to match ranolazine (1 tablet twice daily) during a 4-week run-in period. Participants with at least 85% adherence to documentation requirements (angina frequency and sublingual nitroglycerin use) over the last 21 days of the placebo run-in period will be randomized to the treatment period. Treatment Period: Placebo to match ranolazine (Day 1: 1 tablet in the evening; Days 2-7: 1 tablet twice daily; 2 tablets twice daily thereafter) for up to 8 weeks.
RanolazineRanolazine placeboQualifying phase: Participants will enter a 2-week washout period if needing to discontinue antianginal drugs (except beta-blockers) followed by placebo to match ranolazine (1 tablet twice daily) during a 4-week run-in period. Participants with at least 85% adherence to documentation requirements (angina frequency and sublingual nitroglycerin use) over the last 21 days of the placebo run-in period will be randomized to the treatment period. Treatment period: Ranolazine tablets (Day 1: 1 × 500 tablet in the evening; Days 2-7: 1 × 500 mg twice daily; 2 × 500 mg twice daily thereafter) for up to 8 weeks.
RanolazineRanolazineQualifying phase: Participants will enter a 2-week washout period if needing to discontinue antianginal drugs (except beta-blockers) followed by placebo to match ranolazine (1 tablet twice daily) during a 4-week run-in period. Participants with at least 85% adherence to documentation requirements (angina frequency and sublingual nitroglycerin use) over the last 21 days of the placebo run-in period will be randomized to the treatment period. Treatment period: Ranolazine tablets (Day 1: 1 × 500 tablet in the evening; Days 2-7: 1 × 500 mg twice daily; 2 × 500 mg twice daily thereafter) for up to 8 weeks.
Primary Outcome Measures
NameTimeMethod
Average Weekly Angina Frequency Over the Last 6 Weeks of Treatment6 weeks

Average weekly angina frequency was defined as the total number of angina episodes reported during the last 6 weeks of treatment divided by 6 weeks.

For subjects who terminated with less than 6 weeks of treatment, frequency was calculated as the total number of angina episodes reported during the treatment period divided by the subject's actual duration of treatment.

Secondary Outcome Measures
NameTimeMethod
Change From Baseline in the Short-Form 36® (SF-36) Mental and Physical Component ScoresUp to 8 weeks

The range of each health domain score is 0-100, with 0 indicating a poorer health state and 100 indicating a better health state. An increase in score indicates an improvement in health state. Participants were asked to complete the survey at randomization (prior to receiving treatment), and at end of treatment visit (Week 8) or early study drug discontinuation or early termination visit. The survey asked participants for responses specific to the preceding 4 weeks prior to completing the survey.

Average Weekly Frequency of Sublingual Nitroglycerin Use Over the Last 6 Weeks of Treatment6 weeks

Average weekly frequency of sublingual nitroglycerin use was defined as the total number reported during the last 6 weeks of treatment divided by the duration corresponding to the last 6 weeks of treatment.

Percentage of the Last 6 Weeks on Treatment During Which the Angina Frequency Was ≤ 50% of the Baseline Average Weekly Angina Frequency6 weeks
Percentage of Weeks Participants Achieved at Least a 50% Reduction in Angina Frequency6 weeks

For each participant, the percentage of the last 6 weeks on treatment during which the angina frequency was less than or equal to 50% of the baseline average weekly angina frequency was determined.

Patient's Global Impression of Change (PGIC) Scale Score8 weeks

The PGIC was completed at the end of treatment/last visit.The PGIC scale measures the change in the participant's overall status since the beginning of the study on a scale ranging from 1 (no change or worse) to 7 (very much improved).

Trial Locations

Locations (131)

State Institution of Healthcare Perm Regional Hospital for War Veterans

🇷🇺

Perm, Russian Federation

Minneapolis Heart Institute Foundation

🇺🇸

Minneapolis, Minnesota, United States

Med-Tech Research

🇺🇸

Houston, Texas, United States

National Cardiology Center, Cardiology Clinic - III

🇧🇬

Sofia, Bulgaria

Poliklinika Modrany - Kardiologie

🇨🇿

Praha 4, Czech Republic

Multiprofile Clinical Hospital of Tbilisi #2 LTD

🇬🇪

Tbilisi, Georgia

KO-MED Marek Konieczny

🇵🇱

Puławy, Lubelskie, Poland

Instytut Kardiologii

🇵🇱

Warszawa, Mazowieckie, Poland

Cardiology and Medicine Clinic

🇺🇸

Little Rock, Arkansas, United States

Cross Country Cardiology

🇺🇸

Edgewater, New Jersey, United States

Wellmont Cardiovascular Associates Heart Institute

🇺🇸

Johnson City, Tennessee, United States

Sankt Johannes-Hospital Dortmund

🇩🇪

Dortmund, Germany

Ziv Medical Center

🇮🇱

Safed, Israel

Clinical Trials Management, LLC

🇺🇸

Mandeville, Louisiana, United States

Baptist Heart Specialist

🇺🇸

Jacksonville, Florida, United States

MHAT "Vita", Cardiology Department

🇧🇬

Sofia, Bulgaria

London Road Diagnostic Clinic and Medical Centre

🇨🇦

Ontario, Canada

Topsail Road Medical Clinic

🇨🇦

Saint John's, Canada

Vojenska Nemocnice Brno

🇨🇿

Brno, Czech Republic

Clinic "Guli"

🇬🇪

Tbilisi, Georgia

State Institution "Gomel regional clinical hospital"

🇧🇾

Gomel, Belarus

MHAT "Tsar Boris III"

🇧🇬

Sofia, Bulgaria

Montreal Heart Institute

🇨🇦

Montreal, Canada

Centrum klinického výzkumu, s.r.o.

🇨🇿

Príbram, Czech Republic

Nemocnice Slaný

🇨🇿

Slaný, Czech Republic

Moscow State University of Medicine and Dentistry based on Moscow City Clinical Hospital #71

🇷🇺

Moscow, Russian Federation

City Clinical Hospital named after S.P.Botkin

🇷🇺

Moscow, Russian Federation

Praxis Fur Innere Medizin Kardiologie, Pneumologic und Allergologie

🇩🇪

Mannheim, Germany

MULTI-MED PLUS Sp. z o.o.

🇵🇱

Lódz, Lodzkie, Poland

Krakowski Szpital Specjalistyczny im.JPII

🇵🇱

Krakow, Poland

State Inst Rep Scientific and Practical center

🇧🇾

Minsk, Belarus

UMHAT "Tsaritsa Yoanna" - ISUL, Cardiology Clinic

🇧🇬

Sofia, Bulgaria

Military Medical Academy, Clinic of Cardiology and Intesive Care

🇧🇬

Sofia, Bulgaria

High Desert Medical Group

🇨🇦

Lancaster, Canada

Cardiocentrum Kladno s.r.o.

🇨🇿

Kladno, Czech Republic

Universitätsklinikum Göttingen

🇩🇪

Göttingen, Germany

Universitätsmedizin Mannheim

🇩🇪

Mannheim, Germany

Medical centre "Delis", LLC

🇷🇺

Kirovsk, Russian Federation

Regional Clinical Hospital named after N.N.Burdenko

🇷🇺

Penza, Russian Federation

State Healthcare institution of Moscow"Cardiology Dispensary #2"

🇷🇺

Moscow, Russian Federation

Federal State Institution "Outpatient department #3" of President Management department of Russian Federation

🇷🇺

Moscow, Russian Federation

Cardio-Reanimation Clinic LTD

🇬🇪

Tbilisi, Georgia

Emergency Cardiology Center by Academician G. Chapidze LTD

🇬🇪

Tbilisi, Georgia

Tbilisi Heart and Vascular Clinic LTD

🇬🇪

Tbilisi, Georgia

Städtische Kliniken Bielefeld

🇩🇪

Bielefeld, Germany

Gemeinschaftspraxis fur Kardiologie

🇩🇪

Heidelberg, Germany

Specjalistyczna Praktyka Lekarska Leszek Bryniarski

🇵🇱

Kraków, Malopolskie, Poland

NZOZ Revita Poradnia Kardiologiczna

🇵🇱

Kraków, Malopolskie, Poland

NZOZ Sródmiescie Sp z o.o.

🇵🇱

Gdynia, Pomorskie, Poland

S.P. Specjalistyczny Szpital Zachodni im.JP II

🇵🇱

Grodzisk, Mazowiecki, Poland

Pomorskie Centra Kardiologiczne S.A.

🇵🇱

Gdansk, Poland

Synexus SCM Sp. z o.o. Oddział w Warszawie

🇵🇱

Warszawa, Poland

Educational Institution of Higher Vocational Education "Smolensk State Medical Academy" on the base of Municipal Medicoprophylactic Institution "Hospital of Emergency Medical Care",

🇷🇺

Smolensk, Russian Federation

Saint-Petersburg State Healthcare Institution

🇷🇺

St. Petersburg, Russian Federation

Municipal Institution of Healthcare "Clinical Hospital #8 of Yaroslavl"

🇷🇺

Yaroslavl, Russian Federation

Central Clinical Hospital of Ukrzaliznitsia, Cardiology department

🇺🇦

Kharkiv, Ukraine

SI Odessa Regional Cardiological Dispensary

🇺🇦

Odessa, Ukraine

City Hospital #38 named after Semashko N.A

🇷🇺

Pushkin, St. Petersburg, Russian Federation

Federal State Institution "National Research Center for Preventive Medicine"

🇷🇺

Moscow, Russian Federation

Non-state Institution of healthcare "Department hospital on station Kemerovo of OAO "Russian Railway"

🇷🇺

Kemerovo, Russian Federation

Institution and Address: "Medical Research Institute", LLC

🇷🇺

St. Petersburg, Russian Federation

Autonomous healthcare institution of Voronezh region "Voronezh regional clinic consultative and diagnostic centre"

🇷🇺

Voronezh, Russian Federation

Cardiology Clinic, Clinical Center Serbia

🇷🇸

Belgrade, Serbia

Cardioconsult, s.r.o.

🇸🇰

Bratislava, Slovakia

Kardiovaskulárne centrum, s.r.o.

🇸🇰

Bratislava, Slovakia

KARDIOMED, s.r.o.

🇸🇰

Lučenec, Slovakia

Kyiv City Clinical Hospital #1, Department of Emergency Cardiology

🇺🇦

Kyiv, Ukraine

Department of Diabetology of National Medical Academy of Postgraduate Education named after P.L.Shupyk based on Day Time Hospital of Administration of Medical Service and Rehabilitation of "ARTEM" SHC

🇺🇦

Kyiv, Ukraine

State Budget Educational Institution of High Professional Education First Moscow State Medical University... #1, Cardiology Clinic, Hospital Therapy Department

🇷🇺

Moscow, Russian Federation

FGU Central Clinical Hospital with Polyclinic of President Administrative Department of RF

🇷🇺

St. Petersburg, Russian Federation

State Novosibirsk Regional Clinical Hospital

🇷🇺

Novosibirsk, Russian Federation

State Healthcare institution "Municipal Out-patient Clinic #109"

🇷🇺

St. Petersburg, Russian Federation

ALIAN, s.r.o.

🇸🇰

Bardejov, Slovakia

CARDIO D&R, s.r.o.

🇸🇰

Košice, Slovakia

Kharkiv Medical Academy of Postgraduate Education, Department of cardiology and functional diagnostics based on City Clinical Hospital #8, Department of Cardiology #2

🇺🇦

Kharkiv, Ukraine

Central polyclinic of Pechersk district, Department of cardiology

🇺🇦

Kyiv, Ukraine

State healthcare institution of Moscow "City Clinical hospital#15 named after O.M.Filatov"

🇷🇺

Moscow, Russian Federation

First Moscow State Medical University I.M. Sechenov

🇷🇺

Moscow, Russian Federation

Moscow City Clinical Hospital #51

🇷🇺

Moscow, Russian Federation

Federal State Educational Institution of High Professional Education "Military Medical Academy n.a. S.M. Kirov" of the Ministry of Defence of Russia

🇷🇺

St. Petersburg, Russian Federation

Federal Heart, Blood and Endocrinology Centre n.a. Almazov

🇷🇺

St. Petersburg, Russian Federation

University Klinicni Center Ljubljana

🇸🇮

Ljubljana, Slovenia

General Hospital Murska Sobota

🇸🇮

Murska Sobota, Slovenia

State Institution of Moscow Healthcare "City Clinical Hospital named after S.P. Botkin"

🇷🇺

Moscow, Russian Federation

Moscow State Institution of Health "City Clinical Hospital #81"

🇷🇺

Moscow, Russian Federation

State Healthcare Institution "Ryazan regional clinical cardiological dispensary"

🇷🇺

Ryazan, Russian Federation

"Clinical hospital named after S.R.Mirotvortsev"

🇷🇺

Saratov, Russian Federation

International Medical Center "SOGAZ", LLC

🇷🇺

St. Petersburg, Russian Federation

Institute of Cardiovascular Diseases

🇷🇸

Sremska Kamenica, Serbia

Kardiocentrum Nitra, s.r.o.

🇸🇰

Nitra, Slovakia

University Clinic of Respiratory and Allergic Diseases Golnik

🇸🇮

Golnik, Slovenia

Donetsk National Medical University, Department of Internal Medicine #1 based on Department of Emergency Cardiology and Rehabilitation of Institute of Urgent and Recovery Surgery named after V. K. Gusak

🇺🇦

Donetsk, Ukraine

Kyiv city clinical hospital #5

🇺🇦

Kyiv, Ukraine

Lviv National Medical University named after Danylo Halytsky, Department of Propaedeutics of Internal Medicine #1 based on Polyclinic Department of Municipal City Clinical Hospital #5

🇺🇦

Lviv, Ukraine

Merced Heart Associates

🇺🇸

Merced, California, United States

Spectrum Clinical Research Institute, Inc

🇺🇸

Moreno Valley, California, United States

South Florida Research Solutions, LLC

🇺🇸

Hollywood, Florida, United States

Masters of Clinical Research, Inc.

🇺🇸

Augusta, Georgia, United States

Columbus Cardiology Associates

🇺🇸

Columbus, Georgia, United States

Central Cardiology Associates

🇺🇸

Elizabethtown, Kentucky, United States

Research Integrity, LLC

🇺🇸

Owensboro, Kentucky, United States

Diagnostic Consultative Center, Ascendent Cardiological Out-Patient Office

🇧🇬

Sofia, Bulgaria

Kore CV Research

🇺🇸

Jackson, Tennessee, United States

Humble Cardiology Associates

🇺🇸

Humble, Texas, United States

Aniol Gupta MD

🇨🇦

Toronto, Ontario, Canada

Dr. Roger Labonté Professional Medicine Corp.

🇨🇦

Sudbury, Ontario, Canada

SKDS Research Inc

🇨🇦

New Market, Ontario, Canada

Montréal General Hospital

🇨🇦

Montreal, Quebec, Canada

Fakultní Nemocnice v Motole

🇨🇿

Praha 5, Czech Republic

Corintez s.r.o.

🇨🇿

Praha 5, Czech Republic

Tbilisi State Medical University Alexandre Aladashvili University Clinic

🇬🇪

Tbilisi, Georgia

Amtel Hospital First Clinical LLC

🇬🇪

Tbilisi, Georgia

Charité Campus Virchow Klinikum

🇩🇪

Berlin, Germany

Kaplan Medical Center

🇮🇱

Rehovot, Israel

Barzilai Medical Center, Cardiology Dept.

🇮🇱

Ashkelon, Israel

Assaf Harofeh Medical Centre

🇮🇱

Be'er Ya'aqov, Israel

Tel Aviv Souraski Medical Center

🇮🇱

Tel Aviv, Israel

Niepubliczny Zakład Opieki Zdrowotnej Przychodnia Zdrowia "Zadębie"

🇵🇱

Skierniewice, Lodzkie, Poland

Slaskie Centrum Chorób Serca w Zabrzu

🇵🇱

Zabrze, Poland

Altay Regional Cardiologycal Dispensary

🇷🇺

Barnaul, Russian Federation

Centrum Badawcze Współczenej Terapii

🇵🇱

Warszawa, Poland

"Chita State Medical Academy" Curative-Diagnostic Clinic department

🇷🇺

Chita, Russian Federation

Municipal Institution of Healthcare "Kemerovo Cardiology Dispensary"

🇷🇺

Kemerovo, Russian Federation

Sverdlovsky Regional Clinical Hospital of Wars Veterans

🇷🇺

Ekaterinburg, Russian Federation

State Institution of Healthcare "City Hospital #40 of Kurortniy administrative district

🇷🇺

St. Petersburg, Russian Federation

SI "Institute of Gerontology of AMS of Ukraine"

🇺🇦

Kyiv, Ukraine

Sacramento Heart and Vascular Research Center

🇺🇸

Sacramento, California, United States

Shaare Zedek Medical Center

🇮🇱

Jerusalem, Israel

Clinical Research of Central Florida

🇺🇸

Winter Haven, Florida, United States

Alexandria Cardiology Clinic

🇺🇸

Alexandria, Louisiana, United States

Endeavor Medical Research, PLC

🇺🇸

Alpena, Michigan, United States

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