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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03082937
Other study ID # A4250-007
Secondary ID 2016-002923-27
Status Completed
Phase Phase 1
First received
Last updated
Start date January 31, 2017
Est. completion date March 8, 2017

Study information

Verified date March 2024
Source Ipsen
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary objectives of the study are to assess the mass balance recovery after a single dose of carbon-14 [14C]-A4250 as a capsule and to provide plasma, urine and faecal samples for metabolite profiling and structural identification in healthy male subjects.


Recruitment information / eligibility

Status Completed
Enrollment 6
Est. completion date March 8, 2017
Est. primary completion date March 8, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 30 Years to 65 Years
Eligibility Inclusion Criteria: 1. Healthy males 2. Age 30 to 65 years of age 3. Body mass index of 18.0 to 35.0 kg/m2 or, if outside the range, considered not clinically significant by the investigator 4. Must be willing and able to communicate and participate in the whole study 5. Must have regular bowel movements (i.e., average stool production of =1 and =3 stools per day) 6. Must provide written informed consent 7. Must agree to use an adequate method of contraception Exclusion Criteria: 1. Subjects who have received any IMP in a clinical research study within the previous 3 months prior to screening 2. Subjects who are study site employees, or immediate family members of a study site or sponsor employee 3. Subjects who have previously been enrolled in this study 4. History of any drug or alcohol abuse in the past 2 years 5. Regular alcohol consumption in males >21 units per week (1 unit = ½ pint beer, 25 mL of 40% spirit or a 125 mL glass of wine) 6. Current smokers and those who have smoked within the last 12 months. A confirmed positive urine cotinine test at screening or admission 7. Current users of e-cigarettes and nicotine replacement products and those who have used these products within the last 12 months 8. 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. No occupationally exposed worker, as defined in the Ionising Radiation Regulations 1999, shall participate in the study 9. Subjects who do not have suitable veins for multiple venepunctures/cannulation as assessed by the investigator at screening 10. Clinically significant abnormal biochemistry, haematology or urinalysis as judged by the investigator 11. Confirmed positive drugs of abuse test result at screening or admission 12. Positive hepatitis B surface antigen (HBsAg), hepatitis C virus antibody (HCV Ab) or human immunodeficiency virus (HIV) results 13. Evidence of renal impairment at screening, as indicated by an estimated creatinine clearance (CLcr) of <90 mL/min using the Cockcroft-Gault equation 14. History of cardiovascular, renal, hepatic, chronic respiratory or GI disease as judged by the investigator 15. Serious adverse reaction or serious hypersensitivity to any drug or the formulation excipients 16. Presence or history of clinically significant allergy requiring treatment, as judged by the investigator. Hayfever is allowed unless it is active 17. Donation or loss of greater than 400 mL of blood within the previous 3 months 18. Subjects who are taking, or have taken, any prescribed or over-the-counter drug (other than 4 g per day paracetamol) or herbal remedies in the 14 days before IMP administration. Exceptions may apply on a case by case basis, if considered not to interfere with the objectives of the study, as agreed by the PI and sponsor's medical monitor. 19. Failure to satisfy the investigator of fitness to participate for any other reason

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
3 mg [14C]-A4250 capsule
Each subject will receive a single administration of 3 mg [14C]-A4250 capsule for oral administration containing not more than 4.3 MBq (116 µCi), in the fasted state.

Locations

Country Name City State
United Kingdom Quotient Clinical Ruddington Nottingham

Sponsors (1)

Lead Sponsor Collaborator
Albireo

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary To assess mass balance recovery of total radioactivity in urine Amount excreted (Ae) and Ae as a percentage of the administered dose (% Ae), cumulative recovery (CumAe) and cumulative recovery expressed as a percentage of the dose (Cum%Ae) Between pre-dose (admission to 0 hour) and post dose (ending on morning of discharge (up to day 10 depending on if mass balance cumulative recovery >90% or <1% of dose has been collected))
Primary To assess mass balance recovery of total radioactivity in faeces Amount excreted (Ae) and Ae as a percentage of the administered dose (% Ae), cumulative recovery (CumAe) and cumulative recovery expressed as a percentage of the dose (Cum%Ae) Between pre-dose (admission to 0 hour) and post dose (ending on the morning of discharge (up to day 10 depending on if mass balance cumulative recovery >90% or <1% of dose has been collected))
Primary Metabolite profiling of A4250 of plasma using liquid-chromatography-radio-detection with subsequent mass spectrometry as appropriate Identification of the chemical structure of each metabolite accounting for greater than 10% of circulating radioactivity in plasma Between pre-dose and up to 48 hours post dose
Primary Metabolite profiling of A4250 of urine using liquid-chromatography-radio-detection with subsequent mass spectrometry as appropriate Identification of the chemical structure of each metabolite accounting for greater than 10% of the dose in urine Between pre-dose (admission to 0 hour) and post dose (ending on the morning of discharge (up to day 10 depending on if mass balance cumulative recovery >90% or <1% of dose has been collected))
Primary Metabolite profiling of A4250 of faeces using liquid-chromatography-radio-detection with subsequent mass spectrometry as appropriate Identification of the chemical structure of each metabolite accounting for greater than 10% of the dose in faeces Between pre-dose (admission to 0 hour) and post dose (ending on the morning of discharge (up to day 10 depending on if mass balance cumulative recovery >90% or <1% of dose has been collected))
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