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Completed

NCT Number: NCT03067376

A Study Designed to See How [14C]-CORT125134 is Taken up, Broken Down and Removed From the Body

The study was designed to evaluate how CORT125134 is taken up, broken down and removed from the body when given as an oral capsule to healthy subjects.

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Key information

Conditions

Age range

30 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Quotient Clinical

Nottingham, Nottinghamshire, NG11 6JS, United Kingdom

About this study

The study was conducted to determine the recovery of [14C]-CORT125134 after the administration of a single oral dose of [14C]-CORT125134, to determine the routes and rate of elimination of [14C]-CORT125134 and associated radioactivity from the body, and to measure concentrations of radioactivity in the blood. Additional objectives of the study were to determine the chemical structure of each significant metabolite in plasma, urine and feces. Safety and tolerability were assessed.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy males or healthy females of non-childbearing potential (surgically sterilized or postmenopausal [defined as a woman of with at least a 12 month history of amenorrhea with a follicle-stimulating hormone (FSH) >40 international units per liter (IU/L) in the absence of a reversible medical iatrogenic cause])
  • Age 30 to 65 years of age
  • A history of regular bowel movements (averaging ≥1 and ≤3 stools per day)
  • Must be willing and able to communicate and participate in the whole study
  • Must provide written informed consent
  • Male participants must agree to use an adequate method of contraception
  • Participants are willing to abide by the study restrictions

Exclusion criteria

  • Participation in a clinical research study within the previous 3 months
  • Participants who have previously been enrolled in this study or participants who have previously been treated with CORT125134
  • History of any drug or alcohol abuse in the past 2 years
  • Regular alcohol consumption in males >21 units per week and females >14 units per week (1 unit = ½ pint beer, 25 milliliter (mL) of 40% spirit or a 125 mL glass of wine)
  • Current smokers and those who have smoked within the last 12 months; this includes cigarettes, e-cigarettes and nicotine replacement products. A breath carbon monoxide reading of greater than 10 parts per million (ppm)
  • Females of childbearing potential (female participants must have a negative urine pregnancy test)
  • Male Participants with pregnant partners
  • Radiation exposure exceeding 5 millisievert (mSv) in the last 12 months or 10 mSv in the last 5 years. The measurement includes exposure from the present study, and diagnostic x rays and other medical exposures, but excludes background radiation. No occupationally exposed worker, as defined in the Ionising Radiation Regulations 1999.
  • Positive drugs of abuse test result
  • Participants who are taking, or have taken, any prescribed or over-the-counter drug (other than 4 grams per day paracetamol) or herbal remedies in the 14 days before study drug administration. Hormone replacement therapy is not permitted

Treatment and study plan

[14C]-CORT125134

Drug

Primary outcomes

  1. Amount of radioactivity eliminated in urine

    Time frame: Day 1 pre-dose to Day 8 post-dose

  2. Amount of radioactivity eliminated in feces

    Time frame: Day 1 pre-dose to Day 8 post-dose

  3. Amount of radioactivity eliminated in urine and feces

    Time frame: Day 1 pre-dose to Day 8 post-dose

  4. Cumulative amount of radioactivity eliminated in urine

    Time frame: Day 1 pre-dose to Day 8 post-dose

  5. Cumulative amount of radioactivity eliminated in feces

    Time frame: Day 1 pre-dose to Day 8 post-dose

  6. Cumulative amount of radioactivity eliminated in urine and feces

    Time frame: Day 1 pre-dose to Day 8 post-dose

  7. Pharmacokinetics (PK) of total radioactivity: lag time (tlag)

    Time frame: Day 1 pre-dose to Day 8 post-dose

  8. PK of total radioactivity: peak plasma concentration (Cmax)

    Time frame: Day 1 pre-dose to Day 8 post-dose

  9. PK of total radioactivity: time to reach maximum observed concentration (tmax)

    Time frame: Day 1 pre-dose to Day 8 post-dose

  10. PK of total radioactivity: area under the plasma concentration-time curve from time zero to time of last measurable concentration (AUClast)

    Time frame: Day 1 pre-dose to Day 8 post-dose

  11. PK of total radioactivity: area under the plasma concentration-time curve from time zero to infinity (AUCinf)

    Time frame: Day 1 pre-dose to Day 8 post-dose

  12. PK of total radioactivity: area under the plasma concentration-time curve extrapolated from time t to infinity as a percentage of total AUC (%AUCextrap)

    Time frame: Day 1 pre-dose to Day 8 post-dose

  13. PK of total radioactivity: first-order elimination rate constant associated with the terminal portion of the curve, determined as the negative slope of the terminal log-linear phase of the drug concentration-time curve (lambda-z)

    Time frame: Day 1 pre-dose to Day 8 post-dose

  14. PK of total radioactivity: elimination half-life (t1/2)

    Time frame: Day 1 pre-dose to Day 8 post-dose

  15. Metabolic profiling and structural identification in plasma, urine and feces

    Time frame: Day 1 pre-dose to Day 8 post-dose

Secondary outcomes

  1. Hematology

    Time frame: Screening, Day 1 pre-dose, Day 8

  2. Clinical chemistry

    Time frame: Screening, Day 1 pre-dose, Day 8

  3. Urinalysis

    Time frame: Screening, Day 1 pre-dose, Day 8

  4. Blood pressure

    Time frame: Screening, Day 1 pre-dose and 2 hours post-dose, Day 8

  5. Heart rate

    Time frame: Screening, Day 1 pre-dose and 2 hours post-dose, Day 8

  6. Electrocardiogram

    Time frame: Screening, Day 1 pre-dose and 2 hours post-dose, Day 8

  7. Percentage of subjects with adverse events

    Time frame: Screening to Day 28

  8. Physical examination

    Time frame: Screening and Day 8

  9. Tlag of CORT125134

    Time frame: Day 1 pre-dose to Day 8 post-dose

  10. Cmax of CORT125134

    Time frame: Day 1 pre-dose to Day 8 post-dose

  11. Tmax of CORT125134

    Time frame: Day 1 pre-dose to Day 8 post-dose

  12. AUClast of CORT125134

    Time frame: Day 1 pre-dose to Day 8 post-dose

  13. %AUCextrap of CORT125134

    Time frame: Day 1 pre-dose to Day 8 post-dose

  14. AUCinf of CORT125134

    Time frame: Day 1 pre-dose to Day 8 post-dose

  15. Lambda-z of CORT125134

    Time frame: Day 1 pre-dose to Day 8 post-dose

  16. T1/2 of CORT125134

    Time frame: Day 1 pre-dose to Day 8 post-dose

  17. Mean Residence Time (MRT) of CORT125134

    Time frame: Day 1 pre-dose to Day 8 post-dose

  18. Apparent oral clearance (CL/F) of CORT125134

    Time frame: Day 1 pre-dose to Day 8 post-dose

  19. Apparent volume of distribution (Vz/F) of CORT125134

    Time frame: Day 1 pre-dose to Day 8 post-dose

  20. Number of metabolites >10% of circulating radioactivity in plasma

    Time frame: Day 1 pre-dose to Day 8 post-dose

  21. Number of metabolites >10% of the dose in urine

    Time frame: Day 1 pre-dose to Day 8 post-dose

  22. Number of metabolites >10% of the dose in feces

    Time frame: Day 1 pre-dose to Day 8 post-dose

Sponsors and collaborators

Lead sponsor

Corcept Therapeutics

Industry

Registry information

Official study title

An Open-label, Single-dose Study Designed to Assess the Mass Balance Recovery, Metabolite Profile and Identification of Metabolite Structures for [14C]-CORT125134 in Healthy Subjects

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Mar 1, 2017
Registry last updated
Aug 9, 2019

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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