- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving 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. mars 2015 oppdatert 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.
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Faktiske)
83
Fase
- Fase 4
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Texas
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San Antonio, Texas, Forente stater
- Research Site
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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 70 år (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
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
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: Dobbelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Sekvens A
|
subkutan injeksjon (5mcg eller 10mcg), to ganger daglig
Andre navn:
oral administrering (100 mg), en gang daglig om morgenen
Andre navn:
subcutaneous injection (5mcg or 10mcg), twice a day
oral administration (100mg), once a day in the morning
|
|
Eksperimentell: Sekvens B
|
subkutan injeksjon (5mcg eller 10mcg), to ganger daglig
Andre navn:
oral administrering (100 mg), en gang daglig om morgenen
Andre navn:
subcutaneous injection (5mcg or 10mcg), twice a day
oral administration (100mg), once a day in the morning
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in Time-averaged Glucose During a 24 Hour Period
Tidsramme: 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
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in Two-hour Postprandial Glucose After the Morning Meal
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 4 Weeks
|
Percentage of patients experiencing minor hypoglycemia with a confirmed glucose <54mg/dL
|
4 Weeks
|
|
Episodes of Hypoglycemia (Baseline to Week 4)
Tidsramme: 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)
Tidsramme: 8 weeks
|
Percentage of patients experiencing minor hypoglycemia with a confirmed glucose <54mg/dL
|
8 weeks
|
|
Episodes of Hypoglycemia (Week 4 to Week 8)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 4 weeks and 8 weeks
|
Number of episodes of hypoglycemia experienced overall during the study
|
4 weeks and 8 weeks
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Samarbeidspartnere
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. august 2008
Primær fullføring (Faktiske)
1. oktober 2009
Studiet fullført (Faktiske)
1. oktober 2009
Datoer for studieregistrering
Først innsendt
4. august 2008
Først innsendt som oppfylte QC-kriteriene
6. august 2008
Først lagt ut (Anslag)
7. august 2008
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
9. april 2015
Siste oppdatering sendt inn som oppfylte QC-kriteriene
20. mars 2015
Sist bekreftet
1. mars 2015
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
- Glukosemetabolismeforstyrrelser
- Metabolske sykdommer
- Sykdommer i det endokrine systemet
- Sukkersyke
- Diabetes mellitus, type 2
- Hypoglykemiske midler
- Fysiologiske effekter av legemidler
- Molekylære mekanismer for farmakologisk virkning
- Enzymhemmere
- Hormoner
- Hormoner, hormonsubstitutter og hormonantagonister
- Proteasehemmere
- Midler mot fedme
- Inkretiner
- Dipeptidyl-Peptidase IV-hemmere
- Sitagliptinfosfat
- Exenatid
Andre studie-ID-numre
- H8O-US-GWCV
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. .