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Dose-finding Study of LIK066 Compared With Placebo or Sitagliptin to Evaluate Change in HbA1c in Patients With Diabetes
2 april 2014 bijgewerkt door: Novartis Pharmaceuticals
A Multi-center, Randomized, Double-blind, Parallel-group Dose-finding Study to Evaluate Change in HbA1c After 12 Weeks Monotherapy With 7 Doses of LIK066 Compared With Placebo or Sitagliptin in Patients With Type 2 Diabetes
The purpose of the study is to evaluate the efficacy, tolerability and short-term safety of LIK066 to support dose selection for phase 3.
Studie Overzicht
Toestand
Ingetrokken
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Fase
- Fase 2
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 75 jaar (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
Inclusion Criteria:
- Confirmed diagnosis of T2DM by standard criteria
- Drug-naïve patients, defined as patients not having received any anti-diabetic medication previously,
- Currently untreated patients , who, after the diagnosis of T2DM, have received anti-diabetic medication for not more than 12 consecutive weeks, and have not received any anti-diabetic treatment within 12 weeks prior to Visit 1
- Patients being treated with mono-therapy for at least 8 consecutive weeks prior to Visit 1 with the following OADs: metformin, dipeptidyl peptidase-4 inhibitors (DPP-4i), SU, glinide, alpha-glucosidase inhibitor (AGI)
- HbA1c ≥ 7 to ≤ 10.5% at Visit 1 for drug-naïve/currently untreated patients
- HbA1c ≥ 7 to ≤ 9.5% at Visit 1 for patients treated with OAD monotherapy
- HbA1c ≥ 7 to ≤ 10.5% at Visit 199 for ALL patients
- Age: ≥18 and ≤ 75 years old at Visit 1
- BMI ≥22 to ≤45 kg/m2 at Visit 1
Exclusion Criteria:
- FPG ≥270 mg/dl (15 mmol/L) for drug-naïve/currently untreated patients or ≥240 mg/dl (13.3 mmol/L) for patients on OAD monotherapy at Visit 1
- Insulin treatment >4 consecutive weeks in the last 6 months, corticosteroid use >7 days in the last 8 weeks, use of growth hormones in the last 6 months, or use of weight control products > 4 weeks in the last 6 months
- History of acute metabolic complications, CV disease, type 1 diabetes mellitus, hepatic disorders, pancreatitis, chronic diarrhea
- Significant lab abnormalities such as TSH outside of normal range, UACR>300 mg/g creatinine, eGFR <60 ml/min/1.73m2, hemoglobin <12 g/L in men and <11 g/L in women, hematuria
- ECG abnormalities including AV block, long QT syndrome or QTc>450 msec for men and >470 msec for women
- History of malignancy
- Women of child-bearing potential not using effective methods of contraception Other protocol-defined inclusion/exclusion criteria may apply
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: Parallelle opdracht
- Masker: Dubbele
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: LIK066 2.5 mg
Patients receive 2.5 mg of LIK066 once daily for 12 weeks
|
Experimental treatment doses
|
|
Experimenteel: LIK066 5 mg
Patients receive 5 mg of LIK066 once daily for 12 weeks
|
Experimental treatment doses
|
|
Experimenteel: LIK066 10 mg
Patients receive 10 mg of LIK066 once daily for 12 weeks
|
Experimental treatment doses
|
|
Experimenteel: LIK066 25 mg
Patients receive 25 mg of LIK066 once daily for 12 weeks
|
Experimental treatment doses
|
|
Experimenteel: LIK066 50 mg
Patients receive 50 mg of LIK066 once daily for 12 weeks
|
Experimental treatment doses
|
|
Experimenteel: LIK066 100 mg
Patients receive 100 mg of LIK066 once daily for 12 weeks
|
Experimental treatment doses
|
|
Experimenteel: LIK066 150 mg
Patients receive 150 mg of LIK066 once daily for 12 weeks
|
Experimental treatment doses
|
|
Actieve vergelijker: Sitagliptin 100 mg
Patients receive 100 mg sitagliptin once daily for 12 weeks
|
Active comparator treatment dose
|
|
Placebo-vergelijker: Placebo
Patients receive placebo for 12 weeks
|
Placebo comparator dose
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Change from baseline in glycated hemoglobin (HbA1c) after 12 weeks
Tijdsspanne: baseline, 12 weeks
|
Change from baseline in HbA1c after 12 weeks of treatment in each of the LIK066 doses and placebo
|
baseline, 12 weeks
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Change from baseline in Fasting Plasma Glucose
Tijdsspanne: baseline, 12 weeks
|
The effect of LIK066 on fasting plasma glucose after 12 weeks of treatment will be evaluated.
|
baseline, 12 weeks
|
|
Change from baseline in urinary glucose to creatinine ratio
Tijdsspanne: baseline, 12 weeks
|
The effect of LIK066 on urinary glucose to creatinine ratio after 12 weeks of treatment will be evaluated
|
baseline, 12 weeks
|
|
Change from baseline in Body weight
Tijdsspanne: baseline, 12 weeks
|
The effect of LIK066 on change in body weight after 12 weeks of treatment will be evaluated.
|
baseline, 12 weeks
|
|
Change from baseline in Blood pressure
Tijdsspanne: baseline, 12 weeks
|
The effect of LIK066 on change in systolic and diastolic blood pressure after 12 weeks of treatment will be evaluated.
|
baseline, 12 weeks
|
|
Change from baseline in postprandial glucose during a meal test
Tijdsspanne: baseline, 12 weeks
|
The effect of LIK066 on change in postprandial glucose during a meal test after 12 weeks of treatment will be evaluated.
|
baseline, 12 weeks
|
|
Change from baseline in beta cell function during a meal test
Tijdsspanne: baseline, 12 weeks
|
The effect of LIK066 on change in beta cell function during a meal test after 12 weeks of treatment will be evaluated.
|
baseline, 12 weeks
|
|
Change from baseline in insulin secretion relative to glucose during a meal test
Tijdsspanne: baseline, 12 weeks
|
The effect of LIK066on change in insulin secretion relative to glucose during a meal test after 12 weeks of treatment will be evaluated.
|
baseline, 12 weeks
|
|
Change from baseline in oral glucose insulin sensitivity during a meal test
Tijdsspanne: baseline, 12 weeks
|
The effect of LIK066 on change in oral glucose insulin sensitivity during a meal test after 12 weeks of treatment will be evaluated.
|
baseline, 12 weeks
|
|
Change from baseline in glucagon-like peptide response during a meal test
Tijdsspanne: baseline, 12 weeks
|
The effect of LIK066 on change in glucagon-like peptide during a meal test after 12 weeks of treatment will be evaluated.
|
baseline, 12 weeks
|
|
Change from baseline in Peptide YY response during a meal test
Tijdsspanne: baseline, 12 weeks
|
The effect of LIK066 on change in peptide YY response during a meal test after 12 weeks of treatment will be evaluated.
|
baseline, 12 weeks
|
|
Number of patients with adverse events to assess safety and tolerability of LIK066
Tijdsspanne: 12 weeks
|
The safety and tolerability of 7 doses of LIK066 after 12 weeks of treatment will be evaluated with number of patients reported for total adverse events, serious adverse events and death.
|
12 weeks
|
|
Change from baseline in renal threshold for glucose excretion
Tijdsspanne: baseline, 12 weeks
|
The effect of LIK066 on renal threshold for glucose excretion will be calculated from glucose values in an overnight urine collection
|
baseline, 12 weeks
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
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 november 2015
Primaire voltooiing (Verwacht)
1 november 2016
Studie voltooiing (Verwacht)
1 november 2016
Studieregistratiedata
Eerst ingediend
1 april 2013
Eerst ingediend dat voldeed aan de QC-criteria
1 april 2013
Eerst geplaatst (Schatting)
4 april 2013
Updates van studierecords
Laatste update geplaatst (Schatting)
3 april 2014
Laatste update ingediend die voldeed aan QC-criteria
2 april 2014
Laatst geverifieerd
1 april 2014
Meer informatie
Termen gerelateerd aan deze studie
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
- Incretines
- Natrium-Glucose Transporter 2-remmers
- Dipeptidyl-peptidase IV-remmers
- Sitagliptinefosfaat
- Licogliflozine
Andere studie-ID-nummers
- CLIK066A2202
- 2012-005793-63 (EudraCT-nummer)
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