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Completed

NCT Number: NCT01415778

Bioequivalence of ICI176,334-1 in Japanese Healthy Male Subjects

The purpose of this study is to investigate the bioequivalence of ICI176,334-1 in Japanese healthy male subjects.

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Key information

Conditions

Age range

20 year–45 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

About this study

Bioequivalence study of ICI176,334-1 in Japanese healthy male subjects - evaluation of bioequivalence of ICI176,334-1 and Casodex 80 mg tablet -

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Provision of signed and dated, written informed consent prior to any study specific procedures
  • Japanese healthy male subjects aged 20 to 45 years
  • Male subjects should be willing to use barrier contraception ie, condoms, until 3 months after the last dose of investigational product
  • Have a body mass index (BMI) between 17 and 27 kg/m2
  • Eligible based on the physical findings, supine BP, pulse rate, ECG and laboratory assessments, as judged by the investigator(s)

Exclusion criteria

  • Presence of any disease under medical treatment
  • History or presence of cardiovascular, respiratory, hepatic, renal, gastrointestinal, immunological, blood, endocrine, neurological or mental disease to interfere with absorption, distribution, metabolism or excretion of drugs judged by investigator(s)
  • Presence of any infectious disease, such as bacteria, virus and fungus
  • Presence of allergic disorder, such as asthma, pollen disease or atopic dermatitis, and judged as necessary any medical treatment
  • Any large surgical history of gastrointestinal tract such as gastric/intestinal resection or suturation

Treatment and study plan

ICI176,334-1

Drug

Subject will receive single dose of ICI176,334-1

Casodex 80 mg tablet

Drug

Subject will receive single dose of Casodex 80 mg tablet

Primary outcomes

  1. To investigate the bioequivalence of ICI176,334-1 by assessment of maximum plasma concentration (Cmax)

    Time frame: Blood samples are taken repeatedly for 72 hours and also taken occasionally up to 672 hours after each dose period

  2. To investigate the bioequivalence of ICI176,334-1 by assessment of time to Cmax (tmax)

    Time frame: Blood samples are taken repeatedly for 72 hours and also taken occasionally up to 672 hours after each dose period

  3. To investigate the bioequivalence of ICI176,334-1 by assessment of area under the plasma concentration curve (AUC)

    Time frame: Blood samples are taken repeatedly for 72 hours and also taken occasionally up to 672 hours after each dose period

  4. To investigate the bioequivalence of ICI176,334-1 by assessment of t1/2 of bicalutamide

    Time frame: Blood samples are taken repeatedly for 72 hours and also taken occasionally up to 672 hours after each dose period

Secondary outcomes

  1. To assess the safety by assessment of adverse event

    Time frame: Screening day up to 35 to 42 days (follow-up)

  2. To assess the safety by assessment of vital signs

    Time frame: Collect prior to treatment and up to 35 to 42 days (follow-up) after the last dose.

  3. To assess the safety by assessment of electrocardiograms (ECGs)

    Time frame: Collect prior to treatment and up to 35 to 42 days (follow-up) after the last dose.

Sponsors and collaborators

Lead sponsor

AstraZeneca

Industry

Registry information

Official study title

Bioequivalence Study of ICI176,334-1 in Japanese Healthy Male Subjects - Evaluation of Bioequivalence of ICI176,334-1 and Casodex 80 mg Tablet -

Important dates

Study start
2011
Primary completion
2011
Study completion
2011
First posted
Aug 12, 2011
Registry last updated
May 30, 2012

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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