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Completed

NCT Number: NCT01124747

A Study to Assess the Systemic Disposition of ASP1585 After Administration of 14C-labeled Drug

The objective of this study is to assess the systemic disposition of ASP1585 after oral administration of 14C-labeled drug 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

Madison, Wisconsin, 53704, United States

About this study

Subjects will receive study drug for 18 days with a radioactive dose of study drug given on Day 15. Blood, urine and feces will be collected to confirm recovery of radioactivity.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Body Mass Index (BMI) between 18 and 32 kg/m2, inclusive and minimum body weight 45 kg
  • Agrees to sexual abstinence or to use a highly effective form of birth control which includes a barrier method throughout the study
  • In good health

Exclusion criteria

  • History of any clinically significant disease
  • History of bowel obstruction, swallowing disorders, gastrointestinal disorders, gastrointestinal surgery, actively bleeding hemorrhoids, or gastric/duodenal ulcers
  • Irregular bowel habits (<1 bowel movement per day)
  • Clinically significant illness within 30 days
  • Received any drug or medicine (prescription or over-the-counter), including topical medications, complementary and alternative medicines and vitamin and mineral supplements within 14 days prior to the first dose of study drug
  • Received any investigational medication during the last 30 days or 5 half-lives, whichever is longer, prior to screening
  • Consumes >10 units of alcohol per week or history of alcoholism or drug/chemical abuse within past 2 years
  • Smokes cigarettes or other nicotine-containing products
  • Anticipates an inability to abstain from alcohol use for 48 hours prior to first dose of study drug or from grapefruit, Seville oranges, star fruit or products containing these items from 72 hours prior to first dose of study drug until end of study
  • Positive drug or alcohol screen at Screening or Day -1
  • Alanine aminotransferase (ALT), aspartate aminotransferase (AST) or gamma-glutamyl transferase (GGT) value of >2x upper limit of normal at Screening or Day -1
  • Known positive for human immunodeficiency virus (HIV), Hepatitis A, Hepatitis B or Hepatitis C
  • Unwilling or unable to swallow large numbers of capsules
  • Significant blood loss, donated one unit of blood or more, or received a transfusion of any blood or blood product within 60 days or donated plasma within 7 days prior to Day -1
  • Known cumulative radiation exposure >5 rems for the whole body, active blood forming organs, ocular lens, and gonads, and >15 rems for other organs
  • Has had nuclear medicine procedures, computed tomography scans, or significant x-rays (other than dental) within the past 12 months, has received radiolabeled material within the last 6 months, or has had significant occupational radiation exposure
  • Has participated in a radiolabled study within the last 6 months or participated in more than one radiolabeled study within the last 12 months

Treatment and study plan

ASP1585

Drug

Oral

14C-Labeled ASP1585

Drug

Oral

Primary outcomes

  1. Excretion of radioactivity in urine

    Time frame: Day 15 and up to Day 24

  2. Excretion of radioactivity in feces

    Time frame: Day 15 and up to Day 24

Secondary outcomes

  1. Radioactivity assessment through analysis of blood samples

    Time frame: Day 15 and up to Day 24

Sponsors and collaborators

Lead sponsor

Astellas Pharma Inc

Industry

Registry information

Official study title

An Open-Label Study to Evaluate the Disposition of 14C-Labeled ASP1585 in Healthy Male Volunteers

Important dates

Study start
2010
Primary completion
2010
Study completion
2010
First posted
May 17, 2010
Registry last updated
May 5, 2014

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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