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Completed

NCT Number: NCT00979368

Safety Study of BMS-816336 in Healthy Male Subjects

The purpose of this study is to evaluate the safety, tolerability and pharmacokinetics following single oral doses of BMS-816336 in healthy male subjects.

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Key information

Age range

18 year–55 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Local Institution

Melbourne, Victoria, 3004, Australia

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy male subjects
  • BMI of 18 to 32 kg/m²
  • Men only, ages 18-55 years

Exclusion criteria

  • Sexually active men not using effective birth control if their partners are WOCBP
  • Any significant acute or chronic medical illness
  • Family history of Gilbert's disease
  • History of Pancreatitis
  • Evidence of organ dysfunction or any clinically significant deviation from normal in physical examination, vital signs, EGG or clinical laboratory determinations
  • QTc interval > 450 msec (corrected for heart rate using Fridericia's correction method, QTcF)
  • Second- or third-degree A-V block or clinically relevant ECG abnormalities
  • History of allergy to 11-β-HSD-1 inhibitors or related compounds
  • Prior exposure to BMS-816336
  • Use of St. John's Wort (Hypericum) within 4 weeks prior to the first dose of study drug and throughout the study
  • Use of an oral, injectable, inhalable or suspension of glucocorticoid agents within 12 weeks of study drug administration
  • Use of any glucocorticoid topical creams within 4 weeks of study drug administration
  • Use of oral, injectable, or topical androgen agent within 12 weeks prior to enrollment

Treatment and study plan

BMS-816336

Drug

Suspension, Oral, 15 mg Active, Once on Day 1 only, 4 days

Placebo

Drug

Suspension, Oral, 0 mg, Once on Day 1 only, 4 days

Primary outcomes

  1. Exposure to the investigational drug will be measured to assess safety and tolerability

    Time frame: Within 72 hours following dosing

Secondary outcomes

  1. To assess the single dose Pharmacokinetics of BMS-816336

    Time frame: During 72 hours following dosing

Sponsors and collaborators

Lead sponsor

Bristol-Myers Squibb

Industry

Registry information

Official study title

Randomized, Placebo-Controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BMS-816336 in Healthy Male Subjects

Important dates

Study start
2009
Primary completion
2010
Study completion
2010
First posted
Sep 18, 2009
Registry last updated
Feb 23, 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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