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

8. november 2012 oppdatert av: 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.

Studieoversikt

Status

Avsluttet

Forhold

Detaljert beskrivelse

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

Intervensjonell

Registrering (Faktiske)

8

Fase

  • Fase 3

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

25 år til 75 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

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.

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: Parallell tildeling
  • Masking: Firemannsrom

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Placebo komparator: Placebo QD
TAK-559 placebo-matchende tabletter, oralt, en gang daglig i opptil 26 uker.
Eksperimentell: TAK-559 32 mg QD
TAK-559 32 mg, tabletter, oralt, en gang daglig i opptil 26 uker.

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Endring fra baseline i glykosylert hemoglobin.
Tidsramme: Siste besøk.
Siste besøk.

Sekundære resultatmål

Resultatmål
Tidsramme
Endring fra baseline i fastende plasmaglukose.
Tidsramme: Uke 2, 4, 8, 12, 16, 20 og siste besøk
Uke 2, 4, 8, 12, 16, 20 og siste besøk
Endring fra baseline i seruminsulin.
Tidsramme: Uke 4, 12, 16, 20 og siste besøk.
Uke 4, 12, 16, 20 og siste besøk.
Endring fra baseline i C-peptid.
Tidsramme: Uke 4, 12, 16, 20 og siste besøk.
Uke 4, 12, 16, 20 og siste besøk.
Endring fra baseline i triglyserider.
Tidsramme: Uke 12, 16, 20 og siste besøk.
Uke 12, 16, 20 og siste besøk.
Endring fra baseline i totalkolesterol.
Tidsramme: Uke 12, 16, 20 og siste besøk.
Uke 12, 16, 20 og siste besøk.
Endring fra baseline i high-density lipoprotein.
Tidsramme: Uke 12, 16, 20 og siste besøk.
Uke 12, 16, 20 og siste besøk.
Endring fra baseline i lipoprotein med lav tetthet.
Tidsramme: Uke 12, 16, 20 og siste besøk.
Uke 12, 16, 20 og siste besøk.
Endring fra baseline i lipoprotein med svært lav tetthet.
Tidsramme: Uke 12, 16, 20 og siste besøk.
Uke 12, 16, 20 og siste besøk.
Endring fra baseline i frie fettsyrer.
Tidsramme: Uke 12, 16, 20 og siste besøk.
Uke 12, 16, 20 og siste besøk.
Endring fra baseline i urinalbumin til kreatininforhold.
Tidsramme: Uke 12, 16, 20 og siste besøk
Uke 12, 16, 20 og siste besøk
Change from baseline in glycosylated hemoglobin.
Tidsramme: Weeks 4, 8, 12, 16 and 20
Weeks 4, 8, 12, 16 and 20
Change from base line in apolipoproteins A1 and B 100.
Tidsramme: Final Visit
Final Visit
Change from baseline in thrombosis marker (plasminogen activator inhibitor-1)
Tidsramme: Weeks 4, 12, 16, 20 and Final Visit
Weeks 4, 12, 16, 20 and Final Visit
Change from baseline in thrombosis marker (fibrinogen)
Tidsramme: Weeks 4, 12, 16, 20 and Final Visit
Weeks 4, 12, 16, 20 and Final Visit
Change from baseline in inflammation marker (Interleukin-6).
Tidsramme: 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).
Tidsramme: Weeks 4, 12, 16, 20, and Final Visit
Weeks 4, 12, 16, 20, and Final Visit

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

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. november 2004

Primær fullføring (Faktiske)

1. desember 2004

Studiet fullført (Faktiske)

1. desember 2004

Datoer for studieregistrering

Først innsendt

26. september 2008

Først innsendt som oppfylte QC-kriteriene

29. september 2008

Først lagt ut (Anslag)

30. september 2008

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

12. november 2012

Siste oppdatering sendt inn som oppfylte QC-kriteriene

8. november 2012

Sist bekreftet

1. november 2012

Mer informasjon

Begreper knyttet til denne studien

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