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Efficacy and Safety Study of TAK-559 in Treating Subjects With Type 2 Diabetes Mellitus

8 november 2012 bijgewerkt door: Takeda

A Multicenter, Double-Blind, Randomized, Placebo-Controlled, Parallel Study of the Safety and Efficacy of TAK-559 Compared to Placebo in the Treatment of Patients With Type 2 Diabetes Mellitus

The purpose of this study was to determine the safety and efficacy of TAK-559, once daily (QD), in treating subjects with type 2 diabetes mellitus.

Studie Overzicht

Toestand

Beëindigd

Conditie

Gedetailleerde beschrijving

Insulin is a primary regulator of blood glucose concentrations. A subnormal response to circulating insulin levels at target tissues leads to a decrease in insulin-mediated glucose uptake. Insulin resistance is associated with normal to high insulin levels and is often accompanied by dyslipidemia, a disruption in lipid metabolism resulting in increased triglycerides and low-density lipoprotein levels as well as decreased high-density lipoprotein levels in patients with type 2 diabetes mellitus. In the early stages of insulin resistance, a compensatory mechanism of increased insulin secretion by the pancreas maintains normal to near-normal glucose levels. Once the pancreas fails to maintain the increased insulin output, overt type 2 diabetes mellitus occurs.

TAK-559 is a novel oxyiminoalkanoic acid under investigation for use as an oral agent in the treatment of patients with type 2 diabetes mellitus. TAK-559 has partial peroxisome proliferator-activated receptor-alpha agonist activity, potent peroxisome proliferator-activated receptor-alpha activity, and modest peroxisome proliferator-activated receptor-gamma activity at high concentrations in nonclinical models.

This study was designed to evaluate the safety and glycemic control of TAK-559 in patients with type 2 diabetes mellitus whose symptoms were managed by diet and exercise.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

8

Fase

  • Fase 3

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

25 jaar tot 75 jaar (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria:

  • Was diagnosed with type 2 diabetes mellitus using American Diabetes Association diagnostic criteria, and on a stable dose of an oral anti-diabetic monotherapy prior to Screening A.
  • Had a glycosylated hemoglobin level greater than or equal to 8.0% and less than or equal to 10.0% at Screening B.
  • Had a fasting plasma glucose greater than or equal to 126 mg/dL (7.0 mmol/L) at Screening B.
  • Was taking a stable dose of at least 10 mg of glyburide for at least 10 days prior to Screening B.
  • Had a stable or worsening self-monitoring blood glucose level while taking glyburide.
  • Had a low-density lipoprotein less than 160 mg/dL (4.1 mmol/L) at Screening A.
  • Had a body mass index less than or equal to 45 kg/m2 at Screening A.
  • Was willing to be counseled by the investigator or designee to follow an individualized, weight-maintaining diet during the study period.
  • Had evidence of insulin secretory capacity as demonstrated by a C-peptide concentration of greater than or equal to 1.5 ng/mL (0.50 nmol/L) at Screening A, and if necessary, after a repeat at Screening B.
  • Was able to perform daily self-monitoring blood glucose tests throughout the study.
  • Had a normal thyroid-stimulating hormone level of less than 5.5 uIU/mL (5.5 mIU/L) and greater than or equal to 0.35 uIU/mL (0.35 mIU/L) at Screening A.
  • Was in good health as determined by a physician (ie, via medical history and physical examination), other than a diagnosis of type 2 diabetes mellitus.
  • Had fasting clinical laboratory evaluations within the normal reference range for the testing laboratory, or if not, the results must be deemed not clinically significant by the investigator prior to Randomization.
  • Females were post menopausal, surgically sterile, or using adequate contraception.

Exclusion Criteria:

  • Had been diagnosed with type 1 diabetes mellitus, hemochromatosis, or has a history of ketoacidosis.
  • Had any condition known to invalidate glycosylated hemoglobin results (eg, hemolytic states, hemoglobinopathies).
  • Was required to take or intends to continue taking any disallowed medication, any prescription medication, herbal treatment or over-the counter medication that may interfere with evaluation of the study medication, including:

    • Insulin
    • Oral anti-diabetics other than TAK-559 (including sulfonylureas other than glyburide, alpha-glucosidase inhibitors, metformin)
    • Systemic corticosteroids
    • Warfarin
    • Rifampin
    • St. John's Wort.
    • Thiazolidinediones
    • Peroxisome proliferator-activated receptor agonists
    • Nicotinic Acid
    • Fibrates
  • Had a history of myocardial infarction, coronary angioplasty or bypass graft, unstable angina pectoris, transient ischemic attacks, clinically significant abnormal electrocardiogram, or documented cerebrovascular accident within 6 months prior to Screening A.
  • Had abdominal, thoracic, or vascular surgery within 6 months prior to Screening A that in the investigator's opinion would warrant exclusion from the study.
  • Had a creatine phosphokinase value greater than 3 times the upper limit of normal at Screening A. The creatine phosphokinase value can be retested prior to Randomization if elevated.
  • Had persistent unexplained microscopic or macroscopic hematuria or a history of bladder cancer.
  • Had a triglyceride level greater than 500 mg/dL (5.6 mmol/L) at Screening A.
  • Had any alteration in allowed lipid lowering medication (dose or drug) within 2 months of Randomization, if applicable.
  • Had donated and/or received any blood or blood products within 3 months prior to Randomization.
  • Had a history of drug abuse (defined as illicit drug use) or a history of alcohol abuse (defined as regular or daily consumption of more than 4 alcoholic drinks per day) within 2 years prior to Randomization.
  • Had a systolic BP greater than 140 mm Hg or a diastolic blood pressure of greater than 95 mm Hg at Screening B.
  • Had significant cardiovascular disease including but not limited to, New York Heart Association Functional (Cardiac) Classification III or IV.
  • Had a previous history of cancer, other than basal cell or stage 1 squamous cell carcinoma of the skin, that has not been in remission within 5 years prior to Randomization.
  • Had an alanine transaminase or aspartate transaminase level greater than 3 times the upper limit of normal, active liver disease, or jaundice at Screening A.
  • Had a positive human immunodeficiency virus, hepatitis B surface antigen, or hepatitis B e antigen test at Screening A.
  • Had any other serious disease or condition at Screening A or at Randomization that might affect life expectancy or make it difficult to successfully manage and follow the patient according to the protocol.

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: Verviervoudigen

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Placebo-vergelijker: Placebo QD
TAK-559 placebo-matching tabletten, oraal, eenmaal daags gedurende maximaal 26 weken.
Experimenteel: TAK-559 32 mg QD
TAK-559 32 mg, tabletten, oraal, eenmaal daags gedurende maximaal 26 weken.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Verandering ten opzichte van baseline in geglycosyleerd hemoglobine.
Tijdsspanne: Laatste bezoek.
Laatste bezoek.

Secundaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Verandering ten opzichte van de uitgangswaarde in nuchtere plasmaglucose.
Tijdsspanne: Week 2, 4, 8, 12, 16, 20 en laatste bezoek
Week 2, 4, 8, 12, 16, 20 en laatste bezoek
Verandering ten opzichte van de uitgangswaarde in seruminsuline.
Tijdsspanne: Week 4, 12, 16, 20 en laatste bezoek.
Week 4, 12, 16, 20 en laatste bezoek.
Verandering ten opzichte van baseline in C-peptide.
Tijdsspanne: Week 4, 12, 16, 20 en laatste bezoek.
Week 4, 12, 16, 20 en laatste bezoek.
Verandering ten opzichte van de uitgangswaarde in triglyceriden.
Tijdsspanne: Week 12, 16, 20 en laatste bezoek.
Week 12, 16, 20 en laatste bezoek.
Verandering ten opzichte van de uitgangswaarde in totaal cholesterol.
Tijdsspanne: Week 12, 16, 20 en laatste bezoek.
Week 12, 16, 20 en laatste bezoek.
Verandering ten opzichte van baseline in lipoproteïne met hoge dichtheid.
Tijdsspanne: Week 12, 16, 20 en laatste bezoek.
Week 12, 16, 20 en laatste bezoek.
Verandering ten opzichte van baseline in lipoproteïne met lage dichtheid.
Tijdsspanne: Week 12, 16, 20 en laatste bezoek.
Week 12, 16, 20 en laatste bezoek.
Verandering ten opzichte van de basislijn in lipoproteïne met zeer lage dichtheid.
Tijdsspanne: Week 12, 16, 20 en laatste bezoek.
Week 12, 16, 20 en laatste bezoek.
Verandering ten opzichte van baseline in vrije vetzuren.
Tijdsspanne: Week 12, 16, 20 en laatste bezoek.
Week 12, 16, 20 en laatste bezoek.
Verandering ten opzichte van baseline in albumine/creatinine-ratio in de urine.
Tijdsspanne: Week 12, 16, 20 en laatste bezoek
Week 12, 16, 20 en laatste bezoek
Change from baseline in glycosylated hemoglobin.
Tijdsspanne: Weeks 4, 8, 12, 16 and 20
Weeks 4, 8, 12, 16 and 20
Change from base line in apolipoproteins A1 and B 100.
Tijdsspanne: Final Visit
Final Visit
Change from baseline in thrombosis marker (plasminogen activator inhibitor-1)
Tijdsspanne: Weeks 4, 12, 16, 20 and Final Visit
Weeks 4, 12, 16, 20 and Final Visit
Change from baseline in thrombosis marker (fibrinogen)
Tijdsspanne: Weeks 4, 12, 16, 20 and Final Visit
Weeks 4, 12, 16, 20 and Final Visit
Change from baseline in inflammation marker (Interleukin-6).
Tijdsspanne: Weeks 4, 12, 16, 20 and Final Visit
Weeks 4, 12, 16, 20 and Final Visit
Change from baseline in inflammation marker (C-reactive protein).
Tijdsspanne: Weeks 4, 12, 16, 20, and Final Visit
Weeks 4, 12, 16, 20, and Final Visit

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 2004

Primaire voltooiing (Werkelijk)

1 december 2004

Studie voltooiing (Werkelijk)

1 december 2004

Studieregistratiedata

Eerst ingediend

26 september 2008

Eerst ingediend dat voldeed aan de QC-criteria

29 september 2008

Eerst geplaatst (Schatting)

30 september 2008

Updates van studierecords

Laatste update geplaatst (Schatting)

12 november 2012

Laatste update ingediend die voldeed aan QC-criteria

8 november 2012

Laatst geverifieerd

1 november 2012

Meer informatie

Termen gerelateerd aan deze studie

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