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Completed

NCT Number: NCT04387981

Mass Balance Study of [14C]-Orvepitant Oral Solution in Healthy Male Subjects

This is a single centre, open-label, non-randomised study to assess the mass balance recovery, absorption, metabolism, and excretion of a single oral dose of [14C]-orvepitant in healthy male subjects. It is planned to enrol 6 subjects. Each subject will receive a single dose of 30 mg [14C] orvepitant containing not more than (NMT) 3.7 megabecquerel (MBq) [14C], administered as an oral solution in the fasted state. Subjects will be admitted in the evening on the day prior to [14C]-orvepitant administration and will be dosed in the morning following an overnight fast. It is planned that subjects will remain resident in the clinical unit until 168 hours post-dose (Day 8) when they will be discharged from the clinical unit. Through the resident period samples (blood, urine, faeces) will be collected and analysed for mass balance, total radioactivity, orvepitant levels. Metabolite profiling and ID will also be performed.

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Key information

Conditions

Age range

30 year–65 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Quotient Sciences

Nottingham, United Kingdom

Who can participate

Healthy volunteers accepted: Yes

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

Key Inclusion Criteria:

  • Healthy males
  • Aged 30 to 65 years inclusive at the time of signing informed consent.
  • Body mass index (BMI) of 18.0 to 35.0 kg/m2 as measured at screening.
  • Must provide written informed consent.
  • Must agree to adhere to the contraception requirements

Key Exclusion Criteria:

  • History of any drug or alcohol abuse in the past 2 years.
  • Regular alcohol consumption >21 units per week.
  • Current smokers and those who have smoked within the last 12 months.
  • Radiation exposure, including that from the present study, excluding background radiation but including diagnostic x-rays and other medical exposures, exceeding 5 mSv in the last 12 months or 10 mSv in the last 5 years.
  • Clinically significant abnormal clinical chemistry, haematology, or urinalysis as judged by the Investigator.
  • Subjects with a presence of any of the following at screening: bilirubin, alanine aminotransferase (ALT), or aspartate aminotransferase (AST) >1.5 × the upper limit of normal.
  • Confirmed positive drugs of abuse test result.
  • Positive hepatitis B surface antigen (HBsAg), hepatitis C virus antibody (HCV Ab) or human immunodeficiency virus (HIV) results.
  • Evidence of renal impairment at screening, as indicated by an estimated creatinine clearance (CLcr) of <80 mL/min using the Cockcroft-Gault equation.
  • History of clinically significant cardiovascular, renal, hepatic, chronic respiratory, or GI disease, neurological or psychiatric disorder, as judged by the Investigator.

Treatment and study plan

[14C]-orvepitant

Drug

Oral solution of [14C]-orvepitant

Other names: orvepitant

Primary outcomes

  1. Percentage of radioactive dose recovered in urine and faeces and total percentage

    Time frame: 168 hours

  2. Concentration of total radioactivity in blood and plasma

    Time frame: 168 hours

Sponsors and collaborators

Lead sponsor

Nerre Therapeutics Ltd.

Industry

Registry information

Official study title

A Single Dose Study to Assess the Mass Balance Recovery, Absorption, Metabolism, and Excretion of [14C] Orvepitant in Healthy Male Subjects After Oral Dosing

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
May 14, 2020
Registry last updated
Aug 7, 2020

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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