Mass Balance Study of NV-5138 in Healthy Male Subjects.
An Open-label, Single Dose, Mass Balance Study to Assess the Disposition of [14C]-NV-5138 in Healthy Male Subjects
1 other identifier
interventional
6
1 country
1
Brief Summary
The objective of this study is to assess the mass balance and routes of excretion of total radioactivity after a single oral dose of 1600 mg \[14C\]-NV-5138.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_1 healthy-volunteers
Started Nov 2021
Shorter than P25 for phase_1 healthy-volunteers
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 3, 2021
CompletedStudy Start
First participant enrolled
November 11, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 9, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
December 9, 2021
CompletedFirst Posted
Study publicly available on registry
December 10, 2021
CompletedMarch 15, 2022
March 1, 2022
28 days
November 3, 2021
March 12, 2022
Conditions
Outcome Measures
Primary Outcomes (1)
Cumulative total radioactivity in urine and faeces
The percentage of the radioactive dose recovered in urine, faeces and in total
urine and fecal samples up to 168 hours post dose
Secondary Outcomes (15)
AUCinf for NV-5138, metabolite M8 and total radioactivity in plasma whole blood
up to 168 hours post-dose
AUClast for NV-5138, metabolite M8 and total radioactivity in plasma whole blood
up to 168 hours post-dose
Cmax for NV-5138, metabolite M8 and total radioactivity in plasma whole blood
up to 168 hours post-dose
Tmax for NV-5138, metabolite M8 and total radioactivity in plasma whole blood
up to 168 hours post-dose
Tlast for NV-5138, metabolite M8 and total radioactivity in plasma whole blood
up to 168 hours post-dose
- +10 more secondary outcomes
Study Arms (1)
[14C]-NV-5138
EXPERIMENTAL\[14C\]-NV-5138 oral solution
Interventions
Eligibility Criteria
You may qualify if:
- Healthy males aged 40 to 65 years inclusive at the time of signing informed consent.
- Body mass index of 18.0 to 32.0 kg/m2 as measured at screening
You may not qualify if:
- Subjects who have received any IMP in a clinical research study within the 90 days prior to Day 1
- Subjects who are, or are immediate family members of, a study site or sponsor employee
- Evidence of current SARS-CoV-2 infection
- History of any drug or alcohol abuse in the past 2 years
- Regular alcohol consumption of \>21 units per week and (1 unit = ½ pint beer, or a 25 mL shot of 40% spirit, 1.5 to 2 units = 125 mL glass of wine, depending on type)
- A confirmed positive alcohol breath test at screening or admission
- Current smokers and those who have smoked within the last 12 months. A confirmed breath carbon monoxide reading of greater than 10 ppm at screening or admission
- Current users of e-cigarettes and nicotine replacement products and those who have used these products within the last 12 months
- Subjects with pregnant or lactating partners
- 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 shall participate in the study
- Subjects who have participated in an ADME study involving carbon-14 within 12 months of screening.
- Clinically significant abnormal clinical chemistry, haematology or urinalysis as judged by the investigator. Subjects with Gilbert's Syndrome are not allowed
- Clinically significant abnormalities on vital signs or ECGs as judged by the investigator at screening or pre-dose
- Confirmed positive drugs of abuse test result
- Positive hepatitis B surface antigen (HBsAg), hepatitis C virus antibody (HCV Ab) or human immunodeficiency virus (HIV) antibody results
- +9 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Navitor Pharmaceuticals, Inc.lead
- Supernus Pharmaceuticals, Inc.collaborator
Study Sites (1)
Quotient Sciences
Ruddington, Nottingham, NG116JS, United Kingdom
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 3, 2021
First Posted
December 10, 2021
Study Start
November 11, 2021
Primary Completion
December 9, 2021
Study Completion
December 9, 2021
Last Updated
March 15, 2022
Record last verified: 2022-03