- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg 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. marts 2015 opdateret af: 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.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
83
Fase
- Fase 4
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Texas
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San Antonio, Texas, Forenede Stater
- Research Site
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år til 70 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
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
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Crossover opgave
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Sekvens A
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subkutan injektion (5mcg eller 10mcg), to gange dagligt
Andre navne:
oral administration (100 mg), en gang dagligt om morgenen
Andre navne:
subcutaneous injection (5mcg or 10mcg), twice a day
oral administration (100mg), once a day in the morning
|
|
Eksperimentel: Sekvens B
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subkutan injektion (5mcg eller 10mcg), to gange dagligt
Andre navne:
oral administration (100 mg), en gang dagligt om morgenen
Andre navne:
subcutaneous injection (5mcg or 10mcg), twice a day
oral administration (100mg), once a day in the morning
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Change in Time-averaged Glucose During a 24 Hour Period
Tidsramme: baseline and 8 Weeks
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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).
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baseline and 8 Weeks
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Change in Two-hour Postprandial Glucose After the Morning Meal
Tidsramme: baseline and 8 Weeks
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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)
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baseline and 8 Weeks
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Change in Fasting Blood Glucose After the Morning Meal
Tidsramme: baseline and 8 Weeks
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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)
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baseline and 8 Weeks
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Change in Postprandial Glucagon Area Under the Concentration-time Curve (AUC) After the Morning Meal
Tidsramme: baseline and 8 Weeks
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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)
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baseline and 8 Weeks
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Change in Postprandial Glucagon AUC Excursion After the Morning Meal
Tidsramme: baseline and 8 Weeks
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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)
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baseline and 8 Weeks
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Change in Postprandial Triglyceride AUC After the Morning Meal
Tidsramme: baseline and 8 Weeks
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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)
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baseline and 8 Weeks
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Change in Postprandial Triglyceride AUC Excursion After the Morning Meal
Tidsramme: baseline and 8 Weeks
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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
Tidsramme: baseline and 8 Weeks
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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)
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baseline and 8 Weeks
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Change in Postprandial C-peptide AUC Excursion After the Morning Meal
Tidsramme: baseline and 8 Weeks
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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)
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baseline and 8 Weeks
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Change in Postprandial Insulin AUC After the Morning Meal
Tidsramme: baseline and 8 Weeks
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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)
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baseline and 8 Weeks
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Change in Postprandial Insulin AUC Excursion After the Morning Meal
Tidsramme: baseline and 8 Weeks
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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)
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baseline and 8 Weeks
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Change in Postprandial Active GLP-1 AUC After the Morning Meal
Tidsramme: baseline and 8 Weeks
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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)
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baseline and 8 Weeks
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Change in Postprandial Active GLP-1 AUC Excursion After the Monrning Meal
Tidsramme: baseline and 8 Weeks
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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)
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baseline and 8 Weeks
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Percentage of Patients Experiencing Hypoglycemia (Baseline to Week 4)
Tidsramme: 4 Weeks
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Percentage of patients experiencing minor hypoglycemia with a confirmed glucose <54mg/dL
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4 Weeks
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Episodes of Hypoglycemia (Baseline to Week 4)
Tidsramme: 4 weeks
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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)
Tidsramme: 8 weeks
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Percentage of patients experiencing minor hypoglycemia with a confirmed glucose <54mg/dL
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8 weeks
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Episodes of Hypoglycemia (Week 4 to Week 8)
Tidsramme: 8 weeks
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Number of episodes of hypoglycemia experienced between week 4 and week 8 of the study
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8 weeks
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Percentage of Patients Experiencing Hypoglycemia (Overall)
Tidsramme: 4 weeks and 8 weeks
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Percentage of patients experiencing minor hypoglycemia with a confirmed glucose <54mg/dL
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4 weeks and 8 weeks
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Episodes of Hypoglycemia (Overall)
Tidsramme: 4 weeks and 8 weeks
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Number of episodes of hypoglycemia experienced overall during the study
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4 weeks and 8 weeks
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. august 2008
Primær færdiggørelse (Faktiske)
1. oktober 2009
Studieafslutning (Faktiske)
1. oktober 2009
Datoer for studieregistrering
Først indsendt
4. august 2008
Først indsendt, der opfyldte QC-kriterier
6. august 2008
Først opslået (Skøn)
7. august 2008
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
9. april 2015
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
20. marts 2015
Sidst verificeret
1. marts 2015
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Glukosemetabolismeforstyrrelser
- Metaboliske sygdomme
- Sygdomme i det endokrine system
- Diabetes mellitus
- Diabetes mellitus, type 2
- Hypoglykæmiske midler
- Lægemidlers fysiologiske virkninger
- Molekylære mekanismer for farmakologisk virkning
- Enzymhæmmere
- Hormoner
- Hormoner, hormonsubstitutter og hormonantagonister
- Proteasehæmmere
- Midler mod fedme
- Inkretiner
- Dipeptidyl-Peptidase IV-hæmmere
- Sitagliptin fosfat
- Exenatid
Andre undersøgelses-id-numre
- H8O-US-GWCV
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Type 2 diabetes mellitus
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Instituto Nacional de Ciencias Medicas y Nutricion...Aktiv, ikke rekrutterende
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Endogenex, Inc.Ikke rekrutterer endnuDiabetes mellitus, type 2 | Diabetes | Type 2 diabetes | Type 2 diabetes mellitus (T2DM) | Type 2 Diabetes
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ENBIOSIS BIOTECHNOLOGIESAydin Adnan Menderes University; Izmir University of Economics; Buca Seyfi... og andre samarbejdspartnereRekrutteringType 2 diabetes | Diabetes mellitus type 2Tyrkiet (Türkiye)
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Endogenex, Inc.Ikke rekrutterer endnuDiabetes mellitus, type 2 | Diabetes | Type 2 diabetes mellitus | Type 2 diabetes | Type 2 diabetes
-
El Katib HospitalIkke rekrutterer endnuType 2 diabetes mellitus (T2DM)
-
He Eye HospitalIkke rekrutterer endnu
-
Diabetes Solutions InternationalDexCom, Inc.; Tidepool; MAVEN ProjectRekrutteringType 2 diabetes mellitus (T2DM)Forenede Stater
-
Global Institute of Stem Cell Therapy and ResearchIkke rekrutterer endnu
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Daewoong Pharmaceutical Co. LTD.Ikke rekrutterer endnuT2DM (Type 2 Diabetes Mellitus)
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Zhongda HospitalRekrutteringType 2 diabetes mellitus (T2DM)Kina
Kliniske forsøg med exenatid
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AstraZenecaEli Lilly and CompanyAfsluttetType 2 diabetes mellitusForenede Stater
-
AstraZenecaAfsluttetType 2 diabetes mellitusCanada, Forenede Stater
-
Beijing Chao Yang HospitalAfsluttet
-
AstraZenecaEli Lilly and CompanyAfsluttetType 2 diabetes mellitusKorea, Republikken, Mexico, Tyskland, Grækenland, Argentina, Indien, Australien
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University at BuffaloAmylin Pharmaceuticals, LLC.Afsluttet
-
AstraZenecaEli Lilly and CompanyAfsluttetType 2 diabetes mellitusKorea, Republikken, Kina, Japan, Taiwan, Indien
-
AstraZenecaAfsluttetDiabetes mellitus, type 2Forenede Stater
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AstraZenecaEli Lilly and CompanyAfsluttet
-
AstraZenecaEli Lilly and CompanyAfsluttet
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Metabolic Center of Louisiana Research FoundationAmylin Pharmaceuticals, LLC.AfsluttetPolycystisk ovariesyndromForenede Stater