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OpenTrials
Completed

NCT Number: NCT00828646

Safety Study of Multiple-dose of Gamma-secretase Inhibitor in Healthy Male Japanese and Healthy Elderly Japanese

The purpose of this study is to evaluate the safety profile, tolerability, pharmacokinetics, and pharmacodynamics following 14-day multiple oral doses BMS-708163 in healthy young male Japanese and healthy elderly male and female Japanese subjects

Completed

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Key information

Conditions

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Local Institution

Yokohama, Kanagawa, 2320064, Japan

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy subjects as determined by no clinically significant deviation from normal in medical history, physical examination, ECGs, and clinical laboratory determinations
  • Body Mass Index (BMI) of 19 to 25 kg/m2, inclusive. BMI = weight (kg)/ [height (m)]2
  • Men, ages 20 to 45, and men and women [not of childbearing potential (i.e., who are postmenopausal or surgically sterile)], ages 65 or older. Women are considered surgically sterile only if they have undergone a hysterectomy, bilateral tubal ligation, or bilateral oophorectomy. Women are considered postmenopausal only if they have had amenorrhea for ≥12 consecutive months, or for women on hormone replacement therapy (HRT), if they have a documented serum follicle stimulating hormone (FSH) level > 35 mIU/mL

Exclusion criteria

  • WOCBP
  • Women who are pregnant or breastfeeding
  • Women with a positive pregnancy test on enrollment or prior to administration of investigational product
  • Sexually active fertile men not using effective birth control if their partners are WOCBP
  • Any significant acute or chronic medical illness
  • Any current or recent? medical history of gastrointestinal disease that may affect evaluation of study treatment
  • History of recent major surgery or gastrointestinal surgery that may impact on evaluation or absorption of study drug
  • History of blood donation or blood transfusion within 4 weeks prior to the study treatment
  • Intolerance to oral medication or venous access
  • QTc interval (Bazett's correction) >500 ms at screening
  • Smoking more than 10 cigarettes per day
  • Recent (within 6 months) drug or alcohol abuse as defined in DSM IV
  • Any other sound medical, psychiatric and/or social reason as determined by the investigator
  • Subjects ≥ 65 yr are allowed to have age-related minimum or mild abnormalities in vital sign (i.e. blood pressure) or laboratory tests (i.e. blood sugar, serum cholesterol, or serum triglyceride) as far as they are not deemed signs or consequences of illness or organ dysfunction and a subject of medical treatment
  • Evidence of organ dysfunction or any clinically significant deviation from normal in physical examination, vital signs, ECG or clinical laboratory determinations
  • Positive urine screen for drugs of abuse
  • Positive blood screen for hepatitis C antibody, or HIV or hepatitis B antigen
  • Indicators of abnormal renal function at baseline: any urine protein
  • History of allergy to Gamma-Secretase Inhibitor or related compounds
  • History of any significant drug allergy
  • Prior exposure to BMS-708163
  • Exposure to any investigational drug or placebo within 4 weeks of study drug administration
  • Use of any prescription drugs or over-the-counter acid controllers within 4 weeks prior to study drug administration
  • Use of any other drugs, including over-the-counter medications and herbal preparations, within 2 weeks prior to study drug administration
  • Subjects who are compulsorily detained for treatment of either a psychiatric or physical (eg, infectious disease) illness

Treatment and study plan

BMS-708163

Drug

Capsules, Oral, 50 mg, once daily, 14 days

Placebo

Drug

Capsules, Oral, once daily, 14 days

Primary outcomes

  1. Adverse Events

    Time frame: Within 30 days after the follow-up evaluation on Day 28

Secondary outcomes

  1. Plasma concentration

    Time frame: Day 21

Sponsors and collaborators

Lead sponsor

Bristol-Myers Squibb

Industry

Registry information

Official study title

Placebo-Controlled, Ascending Multiple-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BMS-708163 in Healthy Male Japanese Subjects and a Comparison to Healthy Elderly Japanese Subjects

Acronym: JMAD

Important dates

Study start
2008
Primary completion
2009
Study completion
2009
First posted
Jan 26, 2009
Registry last updated
Jan 7, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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