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Comparison of the Effect of Exenatide Versus Sitagliptin on 24-hour Average Glucose in Patients With Type 2 Diabetes on Metformin or a Thiazolidinedione

20 mars 2015 uppdaterad av: AstraZeneca

Comparison of the Effect of Exenatide vs. Sitagliptin on 24-hour Average Glucose in Patients With Type 2 Diabetes on Metformin or a Thiazolidinedione

This study is designed to compare the short-term effects and mechanisms of action of exenatide with those of sitagliptin when either is added to an oral agent(metformin or a thiazolidinedione [TZD]) in adult patients with type 2 diabetes mellitus(T2DM) with inadequate glycemic control.

Studieöversikt

Studietyp

Interventionell

Inskrivning (Faktisk)

83

Fas

  • Fas 4

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 70 år (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • Have type 2 diabetes
  • Has HbA1c 7.0% to 11.0%, at or within 4 weeks prior to Visit 1.
  • Have a fasting glucose concentration <280 mg/dL at Visit 1
  • Have been treated with a stable dose of immediate or extended release metformin for at least 60 days prior to screening OR TZD (rosiglitazone or pioglitazone) for at least 120 days prior to screening.
  • Are between 18 and 70 years of age, inclusive.
  • Have body mass index ≥25 kg/m2 and ≤45 kg/m2.
  • Have a history of stable body weight (not varying by >10% for at least 3 months prior to screening).
  • Can swallow oral study drug capsule, without splitting or crushing.

Exclusion Criteria:

  • Female patients of childbearing potential (not surgically sterilized and between menarche and 1 year postmenopause) who meet any of the following criteria:

    • Are breastfeeding.
    • Test positive for pregnancy at the time of screening.
    • Intend to become pregnant during the study.
    • Have not practiced a reliable method of birth control (for example, use of oral contraceptives or Norplant®; diaphragms with contraceptive jelly; cervical caps with contraceptive jelly; condoms with contraceptive foam; intrauterine devices; partner with vasectomy; or abstinence) for 3 months prior to screening.
  • Treated with any of the following medications:

    • Insulin, exenatide, pramlintide, sulfonylureas or meglitinides within 3 months of screening
    • Alpha-glucosidase inhibitor within 2 months of screening.
    • Drugs that directly affect gastrointestinal motility, including, but not limited to metoclopramide, cisapride, and chronic macrolide antibiotics.
    • Use of a drug for weight loss (for example, prescription drugs such as orlistat, sibutramine, phentermine, or similar over-the-counter medications) within 3 months prior to Visit 1.
    • Systemic corticosteroids by oral, intravenous, or intramuscular route within 2 months of screening.
  • Have a history of renal transplantation or are currently receiving renal dialysis.
  • Have obvious clinical signs or symptoms of liver disease or acute or chronic hepatitis.
  • Have known active proliferative retinopathy or macular edema expected to need treatment with focal photocoagulation within 3 months.
  • Have an active or untreated malignancy, or have been in remission from clinically significant malignancy (other than basal cell or squamous cell skin cancer, in situ carcinomas of the cervix, or in situ prostate cancer) for less than 5 years.
  • Have had organ transplantation.
  • Have received GLP-1 analogs other than exenatide or DPP-4 inhibitors within the previous 3 months.
  • Have received treatment within the last 30 days with a drug that has not received regulatory approval for any indication at the time of study entry.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Crossover tilldelning
  • Maskning: Dubbel

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Sekvens A
subkutan injektion (5mcg eller 10mcg), två gånger om dagen
Andra namn:
  • Byetta
oral administrering (100 mg), en gång om dagen på morgonen
Andra namn:
  • Januvia
subcutaneous injection (5mcg or 10mcg), twice a day
oral administration (100mg), once a day in the morning
Experimentell: Sekvens B
subkutan injektion (5mcg eller 10mcg), två gånger om dagen
Andra namn:
  • Byetta
oral administrering (100 mg), en gång om dagen på morgonen
Andra namn:
  • Januvia
subcutaneous injection (5mcg or 10mcg), twice a day
oral administration (100mg), once a day in the morning

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in Time-averaged Glucose During a 24 Hour Period
Tidsram: baseline and 8 Weeks
Change in time-averaged glucose during a 24-hour period from baseline to endpoint (i.e., time-averaged glucose over 24 hours at endpoint minus time-averaged glucose over 24 hours at baseline).
baseline and 8 Weeks

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in Two-hour Postprandial Glucose After the Morning Meal
Tidsram: baseline and 8 Weeks
Change in 2 hour post-prandial glucose after the morning meal from baseline to endpoint (i.e., glucose level 2 hours after the morning meal at baseline minus glucose level 2 hours after the morning meal at endpoint)
baseline and 8 Weeks
Change in Fasting Blood Glucose After the Morning Meal
Tidsram: baseline and 8 Weeks
Change in fasting blood glucose after the morning meal from baseline to endpoint (i.e., fasting blood glucose after the morning meal at baseline minus fasting blood glucose after the morning meal at endpoint)
baseline and 8 Weeks
Change in Postprandial Glucagon Area Under the Concentration-time Curve (AUC) After the Morning Meal
Tidsram: baseline and 8 Weeks
Change in Postprandial Glucagon AUC after the morning meal (t=0 to 4 hours) (i.e., Glucagon AUC over the first 4 hours following the morning meal at baseline minus glucagon AUC over the first 4 hours following the morning meal at endpoint)
baseline and 8 Weeks
Change in Postprandial Glucagon AUC Excursion After the Morning Meal
Tidsram: baseline and 8 Weeks
Change in postprandial glucagon AUC excursion after the morning meal (t=0 to 4 hours) (i.e., glucagon AUC excursion for 4 hours following the morning meal at baseline minus glucagon AUC excursion for 4 hours following the morning meal at endpoint)
baseline and 8 Weeks
Change in Postprandial Triglyceride AUC After the Morning Meal
Tidsram: baseline and 8 Weeks
Change in postprandial triglyceride AUC after the morning meal (t=0 to 4 hours) (i.e., postprandial triglyceride AUC after the morning meal at baseline minus postprandial triglyceride AUC after the morning meal at endpoint)
baseline and 8 Weeks
Change in Postprandial Triglyceride AUC Excursion After the Morning Meal
Tidsram: baseline and 8 Weeks
Change in postprandial triglyceride AUC excursion after the morning meal (t=0 to 4 hours) (i.e., postprandial triglyceride AUC excursion after the morning meal at baseline minus postprandial triglyceride AUC excursion after the morning meal at endpoint)
baseline and 8 Weeks
Change in Postprandial C-peptide AUC After the Morning Meal
Tidsram: baseline and 8 Weeks
Change in postprandial C-peptide AUC after the morning meal (t=0 to 4 hours) (i.e., postprandial C-peptide AUC after the morning meal at baseline minus postprandial C-peptide AUC after the morning meal at endpoint)
baseline and 8 Weeks
Change in Postprandial C-peptide AUC Excursion After the Morning Meal
Tidsram: baseline and 8 Weeks
Change in Postprandial C-peptide AUC excursion after the morning meal (t=0 to 4 hours) (i.e., postprandial C-peptide AUC excursion after the morning meal at baseline minus postprandial C-peptide AUC excursion after the morning meal at endpoint)
baseline and 8 Weeks
Change in Postprandial Insulin AUC After the Morning Meal
Tidsram: baseline and 8 Weeks
Change in postprandial insulin AUC after the morning meal (t=0 to 4 hours) (i.e., postprandial insulin AUC after the morning meal at baseline minus postprandial insulin AUC after the morning meal at endpoint)
baseline and 8 Weeks
Change in Postprandial Insulin AUC Excursion After the Morning Meal
Tidsram: baseline and 8 Weeks
Change in Postprandial insulin AUC excursion after the morning meal (t=0 to 4 hours) (i.e., postprandial insulin AUC excursion after the morning meal at baseline minus postprandial insulin AUC excursion after the morning meal at endpoint)
baseline and 8 Weeks
Change in Postprandial Active GLP-1 AUC After the Morning Meal
Tidsram: baseline and 8 Weeks
Change in Postprandial active GLP-1 AUC after the morning meal (t=0 to 4 hours) (i.e., postprandial active GLP-1 AUC after the morning meal at baseline minus postprandial active GLP-1 AUC after the morning meal at endpoint)
baseline and 8 Weeks
Change in Postprandial Active GLP-1 AUC Excursion After the Monrning Meal
Tidsram: baseline and 8 Weeks
Change in Postprandial active GLP-1 AUC excursion after the morning meal (t=0 to 4 hours) (i.e., postprandial active GLP-1 AUC excursion after the morning meal at baseline minus postprandial active GLP-1 AUC excursion after the morning meals at endpoint)
baseline and 8 Weeks
Percentage of Patients Experiencing Hypoglycemia (Baseline to Week 4)
Tidsram: 4 Weeks
Percentage of patients experiencing minor hypoglycemia with a confirmed glucose <54mg/dL
4 Weeks
Episodes of Hypoglycemia (Baseline to Week 4)
Tidsram: 4 weeks
Number of episodes of hypoglycemia experienced during the first 4 weeks of the study
4 weeks
Percentage of Patients Experiencing Hypoglycemia (Week 4 to Week 8)
Tidsram: 8 weeks
Percentage of patients experiencing minor hypoglycemia with a confirmed glucose <54mg/dL
8 weeks
Episodes of Hypoglycemia (Week 4 to Week 8)
Tidsram: 8 weeks
Number of episodes of hypoglycemia experienced between week 4 and week 8 of the study
8 weeks
Percentage of Patients Experiencing Hypoglycemia (Overall)
Tidsram: 4 weeks and 8 weeks
Percentage of patients experiencing minor hypoglycemia with a confirmed glucose <54mg/dL
4 weeks and 8 weeks
Episodes of Hypoglycemia (Overall)
Tidsram: 4 weeks and 8 weeks
Number of episodes of hypoglycemia experienced overall during the study
4 weeks and 8 weeks

Samarbetspartners och utredare

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Sponsor

Samarbetspartners

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 augusti 2008

Primärt slutförande (Faktisk)

1 oktober 2009

Avslutad studie (Faktisk)

1 oktober 2009

Studieregistreringsdatum

Först inskickad

4 augusti 2008

Först inskickad som uppfyllde QC-kriterierna

6 augusti 2008

Första postat (Uppskatta)

7 augusti 2008

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

9 april 2015

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

20 mars 2015

Senast verifierad

1 mars 2015

Mer information

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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