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A Study to Evaluate the Effect of Ranolazine on Postprandial Glucagon in Subjects With Type 2 Diabetes.

28. mars 2014 oppdatert av: Gilead Sciences

A Phase 1, Randomized, Single-blind, Placebo-controlled, Multiple-dose, Two-sequence, Cross-over Study to Evaluate the Effect of Ranolazine on Glucagon Secretion in Subjects With Type 2 Diabetes Mellitus, Followed by An Open-label, Single Dose, Exenatide Active-control Period

To explore the mechanism of action of ranolazine as a potential treatment for type 2 diabetes mellitus (T2DM).

Studieoversikt

Studietype

Intervensjonell

Registrering (Faktiske)

24

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • California
      • Chula Vista, California, Forente stater, 91911
        • Profil Institute for Clinical Research, Inc.
    • Florida
      • Miami, Florida, Forente stater, 33126
        • SeaView Research, Inc
      • Orlando, Florida, Forente stater, 32804
        • Translational Research Institute-Florida Hospital

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 65 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • Males and females, 18 to 65 years old, inclusive
  • Documented history of T2DM for ≥5 years
  • Body mass index (BMI) 20.0 to 40.0 kg/m2, inclusive, at Screening
  • Stable treatment (≥ 12 weeks) with metformin alone, a sulfonylurea alone, a meglitinide alone, or a combination of metformin with either a sulfonylurea or a meglitinide
  • HbA1c ≥ 7.0% and ≤ 10.5%, inclusive, at Screening
  • Fasting glucose within specific ranges, at Screening and after 14 +/-2 days of wash-out from prior oral anti-diabetic agents
  • Fasting serum C-peptide ≥0.8 ng/mL, at Screening
  • Estimated glomerular filtration rate (eGFR)≥60 mL/min/1.73 m2
  • Ability and willingness to comply with all study procedures during the course of the study, including washout from oral anti-diabetic (OAD) agents approximately 2 weeks prior to Day -2 admission
  • Females of childbearing potential must have a negative pregnancy test at Screening and on Day -2 admission and must agree to use highly effective contraception methods from Screening throughout study participation and for 14 days following the last dose of study drug.

Exclusion Criteria:

  • History of type 1 diabetes mellitus or secondary forms of diabetes
  • History of acute diabetes complications
  • Recent or significant heart conditions
  • Uncontrolled hypertension
  • QTc interval > 500 msec by ECG at Screening or on Day -2 admission, a personal or family history of QTc prolongation, congenital long QT syndrome, or use of drugs that prolong the QTc interval, such as Class Ia or Class III antiarrhythmic agents, erythromycin, and certain antipsychotics (eg, ziprasidone)
  • History of severe GI disease (e.g., gastroparesis)
  • History of pancreatitis (acute or chronic)
  • Current consumption of > 14 alcoholic drinks per week, or more than 4 alcoholic drinks on any one day
  • Current regular use of tobacco- or nicotine-containing products in excess of 10 cigarettes per day or equivalent
  • History of substance abuse within 12 months prior to Screening
  • Significant hepatic disease, including, but not limited to, chronic active hepatitis and liver cirrhosis (Child-Pugh Class A, B, or C)
  • History of malignancy within 5 years prior to Screening
  • Significant thyroid disease
  • Treatment with selected medications, as indicated in the protocol
  • Prior treatment with open-label ranolazine or known hypersensitivity or intolerance to ranolazine or its excipients
  • Known hypersensitivity or intolerance to GLP-1 mimetics
  • Known hypersensitivity or intolerance to acetaminophen
  • Aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) > 2.5 X upper limit of normal (ULN)
  • Total Bilirubin (TB) > 2 mg/dL
  • Hemoglobin < 12 g/dL (for males) or < 11 g/dL (for females)
  • Positive for hepatitis B surface antigen
  • Positive for anti-hepatitis C virus antibody
  • Positive for human immunodeficiency virus-1 (HIV-1) antibody
  • Positive urine drug screen
  • Positive alcohol test
  • Donation of blood or blood products to a blood bank, blood transfusion, or participation in a clinical study requiring withdrawal of > 500 mL of blood during the 6 weeks prior to Screening
  • Females who are pregnant or breastfeeding
  • Other condition(s) that, in the opinion of the investigator, would compromise the safety of the subject, would prevent compliance with the study protocol, or would compromise the quality of the clinical study.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Crossover-oppdrag
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: Placebo, Ranolazine, Exenatide
Aktiv komparator: Ranolazine, Placebo, Exenatide

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Area under the concentration-time curve (AUC) of plasma glucagon during the standard meal test (SMT)
Tidsramme: Days 5, 10, and 14
Days 5, 10, and 14

Sekundære resultatmål

Resultatmål
Tidsramme
Plasma glucose, serum insulin, and serum C-peptide AUCs during the SMT
Tidsramme: Days 5, 10, and 14
Days 5, 10, and 14
Collapse under Acetaminophen PK
Tidsramme: Days 5 and 10
Days 5 and 10
Area under the plasma acetaminophen concentration-time curve from time 0 to 240 min (AUC0-240 min)
Tidsramme: Days 5 and 10
Days 5 and 10
Collapse all under ranolazine pharmacokinetics (PK)
Tidsramme: Days 5 and 10
Days 5 and 10
Trough plasma ranolazine concentrations (Ctrough)
Tidsramme: Days 5 and 10
Days 5 and 10
Average plasma ranolazine concentration during a dosing interval at steady state (Css,ave)
Tidsramme: Days 5 and 10
Days 5 and 10
Area under the plasma ranolazine concentration-time curve over dosing interval (AUCtau)
Tidsramme: Days 5 and 10
Days 5 and 10
Apparent elimination half-life (t1/2) of ranolazine
Tidsramme: Days 5 and 10
Days 5 and 10
Adverse events, physical examinations, clinical laboratory determinations, electrocardiograms (ECG), and vital sign assessments.
Tidsramme: From Screening to 7 days after the final dose
From Screening to 7 days after the final dose

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. april 2013

Primær fullføring (Faktiske)

1. september 2013

Studiet fullført (Faktiske)

1. september 2013

Datoer for studieregistrering

Først innsendt

17. april 2013

Først innsendt som oppfylte QC-kriteriene

29. april 2013

Først lagt ut (Anslag)

30. april 2013

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

31. mars 2014

Siste oppdatering sendt inn som oppfylte QC-kriteriene

28. mars 2014

Sist bekreftet

1. mars 2014

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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