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- Klinische proef NCT00729326
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 maart 2015 bijgewerkt door: 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.
Studie Overzicht
Toestand
Voltooid
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Werkelijk)
83
Fase
- Fase 4
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
-
-
Texas
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San Antonio, Texas, Verenigde Staten
- Research Site
-
-
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
18 jaar tot 70 jaar (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
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.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Crossover-opdracht
- Masker: Dubbele
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: Volgorde A
|
subcutane injectie (5mcg of 10mcg), tweemaal per dag
Andere namen:
orale toediening (100 mg), eenmaal daags 's ochtends
Andere namen:
subcutaneous injection (5mcg or 10mcg), twice a day
oral administration (100mg), once a day in the morning
|
|
Experimenteel: Volgorde B
|
subcutane injectie (5mcg of 10mcg), tweemaal per dag
Andere namen:
orale toediening (100 mg), eenmaal daags 's ochtends
Andere namen:
subcutaneous injection (5mcg or 10mcg), twice a day
oral administration (100mg), once a day in the morning
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Change in Time-averaged Glucose During a 24 Hour Period
Tijdsspanne: 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
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Change in Two-hour Postprandial Glucose After the Morning Meal
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
|
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Change in Postprandial Glucagon AUC Excursion After the Morning Meal
Tijdsspanne: 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
Tijdsspanne: 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
|
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Change in Postprandial Triglyceride AUC Excursion After the Morning Meal
Tijdsspanne: 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)
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baseline and 8 Weeks
|
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Change in Postprandial C-peptide AUC After the Morning Meal
Tijdsspanne: 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
Tijdsspanne: 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
|
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Change in Postprandial Insulin AUC After the Morning Meal
Tijdsspanne: 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
Tijdsspanne: 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
|
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Change in Postprandial Active GLP-1 AUC After the Morning Meal
Tijdsspanne: 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
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Change in Postprandial Active GLP-1 AUC Excursion After the Monrning Meal
Tijdsspanne: 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)
Tijdsspanne: 4 Weeks
|
Percentage of patients experiencing minor hypoglycemia with a confirmed glucose <54mg/dL
|
4 Weeks
|
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Episodes of Hypoglycemia (Baseline to Week 4)
Tijdsspanne: 4 weeks
|
Number of episodes of hypoglycemia experienced during the first 4 weeks of the study
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4 weeks
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Percentage of Patients Experiencing Hypoglycemia (Week 4 to Week 8)
Tijdsspanne: 8 weeks
|
Percentage of patients experiencing minor hypoglycemia with a confirmed glucose <54mg/dL
|
8 weeks
|
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Episodes of Hypoglycemia (Week 4 to Week 8)
Tijdsspanne: 8 weeks
|
Number of episodes of hypoglycemia experienced between week 4 and week 8 of the study
|
8 weeks
|
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Percentage of Patients Experiencing Hypoglycemia (Overall)
Tijdsspanne: 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)
Tijdsspanne: 4 weeks and 8 weeks
|
Number of episodes of hypoglycemia experienced overall during the study
|
4 weeks and 8 weeks
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Medewerkers
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start
1 augustus 2008
Primaire voltooiing (Werkelijk)
1 oktober 2009
Studie voltooiing (Werkelijk)
1 oktober 2009
Studieregistratiedata
Eerst ingediend
4 augustus 2008
Eerst ingediend dat voldeed aan de QC-criteria
6 augustus 2008
Eerst geplaatst (Schatting)
7 augustus 2008
Updates van studierecords
Laatste update geplaatst (Schatting)
9 april 2015
Laatste update ingediend die voldeed aan QC-criteria
20 maart 2015
Laatst geverifieerd
1 maart 2015
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Glucosemetabolismestoornissen
- Metabole ziekten
- Endocriene systeemziekten
- Suikerziekte
- Diabetes mellitus, type 2
- Hypoglycemische middelen
- Fysiologische effecten van medicijnen
- Moleculaire mechanismen van farmacologische werking
- Enzymremmers
- Hormonen
- Hormonen, hormoonvervangers en hormoonantagonisten
- Proteaseremmers
- Middelen tegen obesitas
- Incretines
- Dipeptidyl-peptidase IV-remmers
- Sitagliptinefosfaat
- Exenatide
Andere studie-ID-nummers
- H8O-US-GWCV
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .