Efficacy and Safety Study of TAK-128 in Treating Subjects With Diabetic Peripheral Neuropathy

Completed · Phase 2 · Has a placebo group

Conditions studied: Diabetic Neuropathies

In brief

The purpose of this study is to determine the efficacy and safety of TAK-128, once daily (QD), in treating subjects with diabetic peripheral neuropathy.

Key facts

Study ID

NCT00229437

Run by

Takeda

People needed

343

Starts

2005-03-01

Expected to finish

2006-05-01

Last updated by the study team

2012-02-28

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Female subjects of childbearing potential must be nonpregnant, nonlactating and on an acceptable form of contraception.
• The subject has 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.
• The subject has type 1 or 2 diabetes mellitus using World Health Organization Criteria.
• The subject has mild to moderate peripheral neuropathy defined as:
• Clinical neuropathy score greater than or equal to 2.5 on the Michigan Neuropathy Screening Instrument.
• Confirmed abnormality of at least 2 nerve conduction study velocity parameters as defined by the Neurological Core Laboratory.
• Sural sensory nerve potential amplitude greater than or equal to 1 microvolt.
• The subject's glycosylated hemoglobin is less than or equal to 10%.
• The subject is on stable diabetic therapy for at least 3 months prior to randomization.
• The subject is on stable pain medication for at least 6 weeks prior to randomization, if applicable.
• The subject's creatinine level is less than or equal to 2 mg/dL or 176.8 umol/L.
• The subject is willing to follow an American Diabetes Association or similar recommended dietary regimen.

You may not qualify if…

• The subject has a history of other neuropathies due to causes other than diabetes such as alcohol abuse liver or renal disease, uremia, toxic exposure, genetic factors, inflammatory demyelinating diseases, monoclonal gammopathies; or endocrine, metabolic or nutritional disorders (included treated or untreated pernicious anemia).
• The subject has clinical or electrophysiologic evidence of bilateral carpal tunnel syndrome.
• The subject has a significant skin abnormality or ulcerative changes in their lower extremities.
• The subject's body mass index is greater than 40 kg/m2.
• The subject's systolic blood pressure is greater than 160 mm Hg or diastolic blood pressure is greater than 95 mm Hg.
• The subject has a history of myocardial infarction, coronary angioplasty or bypass graft, unstable angina pectoris, transient ischemic attacks, significant electrocardiograms, or documented cerebrovascular accident within 6 months prior to Screening, or is New York Heart Association Functional Cardiac Classification III or IV.
• The subject has an alanine aminotransferase level of greater than 1.5 times the upper limit of normal, active liver disease, or jaundice.
• The subject has a significant, actively treated or unstable pulmonary, gastrointestinal, hepatic, hematologic, musculoskeletal, or endocrine (other than diabetes mellitus or stably treated hypothyroidism) disease.
• The subject has a previous history of cancer, other than basal cell carcinoma, that has not been in remission for at least 5 years prior to the first dose of study drug.
• The subject has taken lipoic acid, linolenic acid (primrose oil), inositol, topiramate, Acetyl-L-Carnitine, nerve growth factors, or capsaicin within 30 days prior to Screening.
• The subject has any other serious disease or condition at Screening or at randomization that might affect life expectancy or make it difficult to successfully manage and follow the subject according to the protocol.
• The subject has 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 the past 2 years.
• The subject has a known hypersensitivity to a compound related to TAK-128.
• Subjects can not use any of the following prescription medications throughout the duration of the study, including:
• Lipoic acid
• Linolenic acid (primrose oil)
• Inositol
• Topiramate
• Acetyl-L-Carnitine
• Nerve growth factors
• Capsaicin
• The subject currently is participating in another investigational study or has participated in an investigational study within the past (30 days or 5 half lives, whichever is longer).

Where it is running

• Study site — Mesa, Arizona, United States
• Study site — Peoria, Arizona, United States
• Study site — Phoenix, Arizona, United States
• Study site — Tucson, Arizona, United States
• Study site — Little Rock, Arkansas, United States
• Study site — Huntington Beach, California, United States
• Study site — La Jolla, California, United States
• Study site — Long Beach, California, United States
• Study site — Los Angeles, California, United States
• Study site — Northridge, California, United States
• Study site — San Francisco, California, United States
• Study site — Torrance, California, United States
• Study site — Tustin, California, United States
• Study site — Aventura, Florida, United States
• Study site — Fort Myers, Florida, United States
• Study site — Hialeah, Florida, United States
• Study site — Miami, Florida, United States
• Study site — Palm Beach Gardens, Florida, United States
• Study site — Plant City, Florida, United States
• Study site — Decatur, Georgia, United States
• Study site — Chicago, Illinois, United States
• Study site — Louisville, Kentucky, United States
• Study site — New Orleans, Louisiana, United States
• Study site — Boston, Massachusetts, United States
• Study site — Ann Arbor, Michigan, United States

Full record on ClinicalTrials.gov

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