Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

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 marzo 2015 aggiornato da: 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.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Effettivo)

83

Fase

  • Fase 4

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Texas
      • San Antonio, Texas, Stati Uniti
        • Research Site

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 18 anni a 70 anni (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione incrociata
  • Mascheramento: Doppio

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Sequenza A
iniezione sottocutanea (5mcg o 10mcg), due volte al giorno
Altri nomi:
  • Byetta
somministrazione orale (100 mg), una volta al giorno al mattino
Altri nomi:
  • Januvia
subcutaneous injection (5mcg or 10mcg), twice a day
oral administration (100mg), once a day in the morning
Sperimentale: Sequenza B
iniezione sottocutanea (5mcg o 10mcg), due volte al giorno
Altri nomi:
  • Byetta
somministrazione orale (100 mg), una volta al giorno al mattino
Altri nomi:
  • Januvia
subcutaneous injection (5mcg or 10mcg), twice a day
oral administration (100mg), once a day in the morning

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in Time-averaged Glucose During a 24 Hour Period
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in Two-hour Postprandial Glucose After the Morning Meal
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 4 Weeks
Percentage of patients experiencing minor hypoglycemia with a confirmed glucose <54mg/dL
4 Weeks
Episodes of Hypoglycemia (Baseline to Week 4)
Lasso di tempo: 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)
Lasso di tempo: 8 weeks
Percentage of patients experiencing minor hypoglycemia with a confirmed glucose <54mg/dL
8 weeks
Episodes of Hypoglycemia (Week 4 to Week 8)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 4 weeks and 8 weeks
Number of episodes of hypoglycemia experienced overall during the study
4 weeks and 8 weeks

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Collaboratori

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio

1 agosto 2008

Completamento primario (Effettivo)

1 ottobre 2009

Completamento dello studio (Effettivo)

1 ottobre 2009

Date di iscrizione allo studio

Primo inviato

4 agosto 2008

Primo inviato che soddisfa i criteri di controllo qualità

6 agosto 2008

Primo Inserito (Stima)

7 agosto 2008

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Stima)

9 aprile 2015

Ultimo aggiornamento inviato che soddisfa i criteri QC

20 marzo 2015

Ultimo verificato

1 marzo 2015

Maggiori informazioni

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Sottoscrivi