Comparison of TAK-875 (Fasiglifam) With Placebo in Participants With Type 2 Diabetes
2016년 3월 4일 업데이트: Takeda
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Daily Oral TAK-875 25 mg and 50 mg Compared With Placebo in Subjects With Type 2 Diabetes
The purpose of this study is to determine the efficacy and safety of TAK-875 (fasiglifam), once daily (QD), in participants with type 2 diabetes mellitus (T2DM).
연구 개요
상세 설명
TAK-875 is being developed at Takeda Development Center, Inc. as an adjunct to diet and exercise to improve glycemic control in patients with T2DM.
This study will investigate TAK-875 in participants with type 2 diabetes mellitus who have been treated with only diet and exercise for at least 12 weeks prior to Screening, who have taken ≤7 days of any antidiabetic agent within the 12 weeks prior to Screening, and whose glycemic control is inadequate.
연구 유형
중재적
등록 (실제)
421
단계
- 3단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 장소
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Guatemala, 과테말라
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Guatemala City, 과테말라
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Quetzaltenango, 과테말라
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Zacapa, 과테말라
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Distrito Federal
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Mexico, Distrito Federal, 멕시코
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Nuevo León
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Monterrey, Nuevo León, 멕시코
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Alabama
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Dothan, Alabama, 미국
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Muscle Shoals, Alabama, 미국
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Arizona
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Goodyear, Arizona, 미국
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Phoenix, Arizona, 미국
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California
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Long Beach, California, 미국
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North Hollywood, California, 미국
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Norwalk, California, 미국
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Palm Springs, California, 미국
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Pismo Beach, California, 미국
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Florida
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Boynton Beach, Florida, 미국
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Bradenton, Florida, 미국
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Coral Gables, Florida, 미국
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Hialeah, Florida, 미국
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Largo, Florida, 미국
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New Port Richey, Florida, 미국
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Orlando, Florida, 미국
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Pembroke Pines, Florida, 미국
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Georgia
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Decatur, Georgia, 미국
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Illinois
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Chicago, Illinois, 미국
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Indiana
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Avon, Indiana, 미국
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Greenfield, Indiana, 미국
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Muncie, Indiana, 미국
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Iowa
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Council Bluffs, Iowa, 미국
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Kansas
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Topeka, Kansas, 미국
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Kentucky
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Lexington, Kentucky, 미국
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Maryland
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Oxon Hill, Maryland, 미국
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Michigan
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Flint, Michigan, 미국
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Mississippi
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Picayune, Mississippi, 미국
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Nebraska
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Omaha, Nebraska, 미국
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New Jersey
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Elizabeth, New Jersey, 미국
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North Carolina
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Charlotte, North Carolina, 미국
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Greensboro, North Carolina, 미국
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Mooresville, North Carolina, 미국
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Morganton, North Carolina, 미국
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Raleigh, North Carolina, 미국
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Ohio
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Maumee, Ohio, 미국
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Oklahoma
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Oklahoma City, Oklahoma, 미국
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Pennsylvania
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Harleysville, Pennsylvania, 미국
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Levittown, Pennsylvania, 미국
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Uniontown, Pennsylvania, 미국
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South Carolina
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Greer, South Carolina, 미국
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Tennessee
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Crossville, Tennessee, 미국
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Texas
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Carrollton, Texas, 미국
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Dallas, Texas, 미국
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El Pasco, Texas, 미국
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Fort Worth, Texas, 미국
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Ft. Worth, Texas, 미국
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Houston, Texas, 미국
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Irving, Texas, 미국
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New Braunfels, Texas, 미국
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San Antonio, Texas, 미국
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Spring, Texas, 미국
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Tomball, Texas, 미국
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Utah
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Salt Lake City, Utah, 미국
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Virginia
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Burke, Virginia, 미국
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Manassas, Virginia, 미국
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Byala, 불가리아
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Plovdiv, 불가리아
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Ruse, 불가리아
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Sofia, 불가리아
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Varna, 불가리아
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Banska Bystrica, 슬로바키아
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Bratislava, 슬로바키아
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Dolny Kubin, 슬로바키아
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Komarno, 슬로바키아
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Levice, 슬로바키아
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Pezinok, 슬로바키아
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Prievidza, 슬로바키아
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Trebisov, 슬로바키아
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Trencin, 슬로바키아
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Zilina, 슬로바키아
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Ciudad Autonoma Buenos Aires, 아르헨티나
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Cordoba, 아르헨티나
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Corrientes, 아르헨티나
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Mendoza, 아르헨티나
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Ciudad Autonoma Buenos Aires
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Ciudad Autonoma de Buenos Aires, Ciudad Autonoma Buenos Aires, 아르헨티나
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Cordoba
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Villa Cabrera, Cordoba, 아르헨티나
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Dnipropetrovsk, 우크라이나
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Kharkiv, 우크라이나
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Kyiv, 우크라이나
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Odesa, 우크라이나
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Simferopol, 우크라이나
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Ternopil, 우크라이나
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Vinnytsia, 우크라이나
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Zaporizhzhia, 우크라이나
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Budapest, 헝가리
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Debrecen, 헝가리
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Kecskemet, 헝가리
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Komarom, 헝가리
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Szikszo, 헝가리
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Zalaegerszeg, 헝가리
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참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
공부할 수 있는 나이
18년 이상 (성인, 고령자)
건강한 자원 봉사자를 받아들입니다
아니
연구 대상 성별
모두
설명
Inclusion Criteria:
- In the opinion of the investigator, the participant is capable of understanding and complying with protocol requirements.
- The participant or, when applicable, the participant's legally acceptable representative signs and dates a written, informed consent form and any required privacy authorization prior to the initiation of any study procedures.
- The participant is male or female and 18 years of age or older with a historical diagnosis of T2DM.
- The participant has been treated with only diet and exercise for at least 12 weeks prior to Screening and has an HbA1c concentration between 7.0 % and 10.5%, inclusive, at Screening.
- The participant has received ≤7 days of any antidiabetic agent within 12 weeks prior to Screening.
- The participant has a body mass index (BMI) ≤45 kg/m^2 at Screening.
- Participants regularly using other, non-excluded medications must be on a stable dose for at least 4 weeks prior to Screening. However, as needed (PRN) use of prescription or over-the-counter medication is allowed at the discretion of the investigator.
- The participant is able and willing to monitor glucose with a home glucose monitor and consistently record his or her own blood glucose concentrations and complete participant diaries.
- A female participant of childbearing potential who is sexually active with a nonsterilized male partner agrees to use routinely adequate contraception from signing of the informed consent throughout the duration of the study and for 30 days after the last dose of study drug.
Additional Inclusion Criteria prior to Randomization
- The participant has an HbA1c concentration between 7.0 and 10.5%, inclusive, and a fasting plasma glucose (FPG) ≤270 mg/dL (≤15.0 mmol/L) at Week -1 Visit. (If the participant does not qualify for randomization based on these criteria, the assessments may be repeated weekly, for a maximum of 2 additional weeks).
- The participant's overall compliance with single-blind study medication during the Placebo Run-in Period is at least 75% and does not exceed 125% based on tablet counts performed by the study staff.
- A female participant of childbearing potential must have a negative urine hCG pregnancy test at Baseline (Visit 4) prior to Randomization and prior to administration of the first dose of double-blind study medication
Exclusion Criteria:
- The participant has received any investigational compound within 30 days prior to Screening or has received an investigational antidiabetic drug within 3 months prior to Screening.
- The participant has been randomized in a previous TAK-875 study.
- The participant is an immediate family member, study site employee, or is in a dependent relationship with a study site employee who is involved in conduct of this study (e.g., spouse, parent, child, or sibling; biological or legally adopted) or may consent under duress.
- The participant donated or received any blood products within 12 weeks prior to Screening or is planning to donate blood during the study.
- The participant has a hemoglobin ≤12 g/dL (≤120 gm/L) for males and ≤10 g/dL (≤100 gm/L) for females at Screening.
- The participant has a systolic blood pressure ≥160 mm Hg or diastolic blood pressure ≥95 mm Hg at Screening (If the participant meets this exclusion criterion, the assessment may be repeated once at least 30 minutes after the initial measurement and decision will be made based on the second measurement).
- The participant has a history of cancer that has been in remission for <5 years prior to Screening. A history of basal cell carcinoma or stage 1 squamous cell carcinoma of the skin is allowed.
- The participant has an alanine aminotransferase (ALT) and/or aspartate aminotransferase (AST) levels >2.0x the upper limit of normal (ULN) at Screening.
- The participant has a total bilirubin level greater than the ULN at Screening. Exception: if a participant has documented Gilbert's Syndrome, the participant will be allowed with an elevated bilirubin level per the investigator's discretion.
- The participant has a serum creatinine ≥1.5 mg/dL(≥133 µmol/L) [males] and ≥1.4 mg/dL (≥124 µmol/L) [females] and/or estimated glomerular filtration rate (GFR) <60 mL/min/1.73m^2 at Screening.
- The participant has uncontrolled thyroid disease.
- The participant has a history of laser treatment for proliferative diabetic retinopathy within 6 months prior to Screening.
- The participant has had gastric banding or gastric bypass surgery within one year prior to Screening.
- The participant has a known history of infection with human immunodeficiency virus (HIV), Hepatitis B virus (HBV), or Hepatitis C virus (HCV).
- The participant had coronary angioplasty, coronary stent placement, coronary bypass surgery, myocardial infarction, unstable angina pectoris, clinically significant abnormal electrocardiogram (ECG), cerebrovascular accident or transient ischemic attack within 3 months prior or at Screening.
- The participant has a history of hypersensitivity, allergies, or has had an anaphylactic reaction(s) to any component of TAK-875.
- The participant has a history of drug abuse (defined as illicit drug use) or a history of alcohol abuse within 2 years prior to Screening.
- The participant received excluded medications prior to Screening or is expected to receive excluded medication.
- If female, the participant is pregnant (confirmed by laboratory testing, i.e., serum human chorionic gonadotropin (hCG), in females of childbearing potential) or lactating or intending to become pregnant before, during, or within 1 month after participating in this study; or intending to donate ova during such time period.
- The participant is unable to understand verbal or written English or any other language for which a certified translation of the approved informed consent is available.
- The participant has any other physical or psychiatric disease or condition that in the judgment of the investigator may affect life expectancy or may make it difficult to successfully manage and follow the participant according to the protocol.
Additional Exclusion Criteria prior to Randomization
- The participant received excluded medications during the Placebo Run-in Period. (Topical and inhaled corticosteroids are allowed).
- The participant has a systolic blood pressure ≥160 mm Hg or diastolic blood pressure ≥95 mm Hg at Baseline (Visit 4) (If the participant meets this exclusion criterion, the assessment may be repeated once at least 30 minutes after the initial measurement and decision will be made based on the second measurement).
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 네 배로
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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위약 비교기: Placebo
Fasiglifam placebo-matching tablets, orally, once daily for up to 24 weeks.
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Fasiglifam 위약 일치 정제
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실험적: Fasiglifam 25 mg
Fasiglifam 25 mg, tablets, orally, once daily for up to 24 weeks.
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파시글리팜 정제
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실험적: Fasiglifam 50 mg
Fasiglifam 50 mg, tablets, orally, once daily for up to 24 weeks.
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파시글리팜 정제
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Change From Baseline in Glycosylated Hemoglobin (HbA1c)
기간: Baseline and Week 24
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The change in the value of glycosylated hemoglobin (the concentration of glucose bound to hemoglobin as a percent of the absolute maximum that can be bound) collected at Week 24 relative to Baseline.
A mixed model repeated measures (MMRM) model with treatment, country, visit and visit by treatment interaction as fixed factors and with Baseline value and Baseline value by visit interaction as covariates with an unstructured covariance structure was used for analysis.
|
Baseline and Week 24
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Incidence of HbA1c <7%
기간: Week 24
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The incidence (percentage of participants with) HbA1c (the concentration of glucose bound to hemoglobin as a percent of the absolute maximum that can be bound) of less than seven percent for target glycemic control at Week 24.
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Week 24
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Change From Baseline in Fasting Plasma Glucose
기간: Baseline and Week 24
|
The change between the fasting plasma glucose value collected at Week 24 relative to Baseline measured in milligrams per deciliter (mg/dL).
A MMRM model with treatment, country, visit and visit by treatment interaction as fixed factors and with Baseline value and Baseline value by visit interaction as covariates with an unstructured covariance structure was used for analysis.
|
Baseline and Week 24
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Change From Baseline in 2-hour Postprandial Glucose (PPG) Following a Meal Tolerance Test (MTT)
기간: Baseline and Week 24
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The change between the value of glucose after a meal, measured by the meal tolerance test collected at Week 24 relative to Baseline.
Meal tolerance test measures blood glucose through blood samples drawn before a meal and 2 hours after the start of the meal measured in millimoles per liter (mmol/L).
An Analysis of Covariance (ANCOVA) model with treatment and country as fixed factors and Baseline value as covariate was used for analysis.
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Baseline and Week 24
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공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
스폰서
수사관
- 연구 책임자: Senior Medical Director, Takeda
간행물 및 유용한 링크
연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.
연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작
2011년 11월 1일
기본 완료 (실제)
2013년 7월 1일
연구 완료 (실제)
2013년 7월 1일
연구 등록 날짜
최초 제출
2011년 10월 18일
QC 기준을 충족하는 최초 제출
2011년 10월 18일
처음 게시됨 (추정)
2011년 10월 20일
연구 기록 업데이트
마지막 업데이트 게시됨 (추정)
2016년 4월 5일
QC 기준을 충족하는 마지막 업데이트 제출
2016년 3월 4일
마지막으로 확인됨
2016년 3월 1일
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .