Phase 1, Open-label Study of the Absorption, Metabolism, and Excretion of [14C]-KW-6356

A Phase 1, Open-label Study of the Absorption, Metabolism, and Excretion of [14C]-KW-6356 Following a Single Oral Dose in Healthy Male Subjects

This is an open-label, single-dose study in healthy male subjects to investigate the absorption, metabolism, and excretion (AME) of KW-6356.

Study Overview

• Status: Completed
• Conditions: Healthy Male Subjects
• Intervention / Treatment: Drug: KW-6356

Detailed Description

Subjects will be screened to assess their eligibility to enter the study within approximately 4 weeks prior to dose administration. Subjects will be confined to the Clinical Research Unit (CRU) for their entire participation in this study. Eight subjects will be enrolled to allow 6 subjects to complete the study. Each subject will report to the CRU and be confined from Day -1 (the day before dosing) through at least Day 8 (168 hours postdose). A single dose of study drug will be administered on Day 1 (0 hour). On Day 8, subjects can be asked to remain as a resident within the CRU for an additional period to allow for ongoing 24-hour urine, fecal, and blood sample collections. These collections can continue up to a maximum of 336 hours postdose (Day 15). Subjects can be discharged prior to Day 15 if the following individual subject discharge criteria have been satisfied: ≥ 90% of the 14C dose recovered in combined urine and feces, and ≤ 1% of the total radioactive dose is recovered in combined excreta (urine and feces) in 3 consecutive 24-hour periods in which a fecal sample is provided.

• Study Type: Interventional
• Enrollment (Actual): 8
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • Wisconsin
    • Madison, Wisconsin, United States, 53704
      • Covance Clinical Research Unit Inc.

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 65 years (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

1. Males, of any race, between 18 and 65 years of age, inclusive.
2. Body mass index between 18.0 and 30.0 kg/m2, inclusive.
3. In good health, determined by no clinically significant findings from medical history, physical examination, 12 lead ECG, vital sign measurements, and clinical laboratory evaluations.
4. Able to sign an ICF and willing to abide by the study restrictions.
5. Will agree to use contraception.
6. History of at least 1 bowel movement per day.

Exclusion Criteria:

1. Any clinically significant illness as determined by the Principal Investigator.
2. History of significant hypersensitivity, intolerance, or allergy to any drug compound, food, or other substance.
3. Have received any investigational drug within 30 days or 5.5 half-lives, whichever is longer, prior to study dosing.
4. History of drug or alcohol abuse or dependence within 2 years prior to signing of ICF.
5. Hospital admission, surgery, within 3 months before investigational product administration.
6. Positive hepatitis B surface antigen or hepatitis C RNA, or positive for acquired human immunodeficiency virus.
7. Positive urine drug screen for drugs of abuse.
8. History of requiring treatment for urinary retention within 3 months before investigational product administration.
9. History of seizures.
10. Subjects with history of, or active suicidal ideation, or suicide attempt.
11. History of stomach or intestinal surgery or resection that would potentially alter absorption and/or excretion of orally administered drugs (uncomplicated appendectomy and hernia repair will be allowed). Subjects with cholecystectomy will not be allowed.
12. Use or intend to use any medications/products known to alter drug absorption, metabolism, or elimination processes, including inducers/inhibitors of CYP3A4 and St. John's wort, within 30 days prior to Day 1.
13. Use or intend to use any prescription medications/products within 30 days or 5.5 half-lives (if known), whichever is longer, prior to Check-in.
14. Use or intend to use slow-release medications/products considered to still be active within 30 days or 5.5 half-lives (if known), whichever is longer, prior to Check-in.
15. Use of any nonprescription medications (for 14 days prior to Check-in).
16. Use of tobacco- or nicotine-containing products within 3 months prior to Check-in, or positive cotinine.
17. Receipt of blood products within 2 months prior to Check-in.
18. Donation of blood (> 200 mL) from 3 months prior to Screening, plasma from 2 weeks prior to Screening, or platelets from 6 weeks prior to Screening.
19. Poor peripheral venous access.
20. Have previously completed or withdrawn from this study or any other study investigating KW-6356, and have previously received the investigational product.
21. Subjects with exposure to significant diagnostic or therapeutic radiation (eg, serial X-ray, computed tomography scan, barium meal) or current employment in a job requiring radiation exposure monitoring within 12 months prior to Check-in.
22. Subjects who have participated in a radiolabeled drug study where exposures are known to the Investigator within the previous 4 months prior to admission to the clinic for this study or participated in a radiolabeled drug study where exposures are not known to the Investigator within the previous 6 months prior to admission to the clinic for this study.
23. Subjects who, in the opinion of the Investigator, should not participate in this study.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Other
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: KW-6356; Single oral dose of carbon-14-KW-6356.	Drug: KW-6356; Single oral dose of KW-6356

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Cmax	Maximum observed concentration (KW-6356 in plasma and total radioactivity in plasma and blood).	Pre-dose up to 168 hours post dose, up to 336 hours post dose.
tmax	Time of maximum observed concentration (KW-6356 in plasma and total radioactivity in plasma and blood).	Pre-dose up to 168 hours post dose, up to 336 hours post dose.
AUC0-t	Area under the drug concentration-time curve from time zero to the last quantifiable concentration (KW-6356 in plasma and total radioactivity in plasma and blood).	Pre-dose up to 168 hours post dose, up to 336 hours post dose.
%AUCextra	Percentage of estimated part for the calculation of AUC0-∞ (KW-6356 in plasma and total radioactivity in plasma and blood).	Pre-dose up to 168 hours post dose, up to 336 hours post dose.
t1/2	Elimination half-life (KW-6356 in plasma and total radioactivity in plasma and blood).	Pre-dose up to 168 hours post dose, up to 336 hours post dose.
kel	Elimination rate constant (KW-6356 in plasma and total radioactivity in plasma and blood).	Pre-dose up to 168 hours post dose, up to 336 hours post dose.
Vz/F	Apparent volume of distribution during terminal phase (KW-6356 in plasma).	Pre-dose up to 168 hours post dose, up to 336 hours post dose.
CL/F	Apparent oral clearance (KW-6356 in plasma).	Pre-dose up to 168 hours post dose, up to 336 hours post dose.
MRT	Mean residence time (KW-6356 in plasma).	Pre-dose up to 168 hours post dose, up to 336 hours post dose.
Whole blood/plasma concentration ratio (total radioactivity in blood and plasma).		Pre-dose up to 168 hours post dose, up to 336 hours post dose.
Aeurine	Cumulative amount excreted in urine (total radioactivity in urine).	Pre-dose up to 168 hours post dose, up to 336 hours post dose.
feurine	Fraction of the dose administered excreted in urine (total radioactivity in urine).	Pre-dose up to 168 hours post dose, up to 336 hours post dose.
Aefeces	Cumulative amount excreted in feces (total radioactivity in feces).	Pre-dose up to 168 hours post dose, up to 336 hours post dose.
fefeces	Fraction of the dose administered excreted in feces (total radioactivity in feces).	Pre-dose up to 168 hours post dose, up to 336 hours post dose.
Aetotal	Total amount excreted (total radioactivity in urine and feces).	Pre-dose up to 168 hours post dose, up to 336 hours post dose.
fetotal	Fraction of the dose administered excreted in urine and feces (total radioactivity in urine and feces).	Pre-dose up to 168 hours post dose, up to 336 hours post dose.
Metabolic profiling and identification (plasma, urine, and feces).		Pre-dose up to 168 hours post dose, up to 336 hours post dose.

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Adverse Events	Number of subjects experiencing an adverse event related to treatment.	From screening through study completion, an average of 6 weeks.
Severe adverse events.	Number of subjects experiencing a severe adverse event related to treatment.	From screening through study completion, an average of 6 weeks.
Serum chemistry, hematology, and urinalysis.	Number of subjects with abnormal laboratory values that are related to treatment.	From screening through study completion, an average of 6 weeks.
Vital signs	Number of subjects with abnormal vital signs that are related to treatment.	From screening through study completion, an average of 6 weeks.
12-lead ECG.	Number of subjects with abnormal ECG that are related to treatment.	From screening through study completion, an average of 6 weeks.
Physical examination.	Number of subjects with abnormal physical exam findings that are related to treatment.	From screening through study completion, an average of 6 weeks.

Collaborators and Investigators

• Sponsor: Kyowa Kirin, Inc.

Study record dates

Study Major Dates

• Study Start (Actual): August 21, 2019
• Primary Completion (Actual): October 2, 2019
• Study Completion (Actual): October 2, 2019

Study Registration Dates

• First Submitted: October 9, 2019
• First Submitted That Met QC Criteria: October 30, 2019
• First Posted (Actual): November 1, 2019

Study Record Updates

• Last Update Posted (Actual): April 25, 2024
• Last Update Submitted That Met QC Criteria: April 24, 2024
• Last Verified: April 1, 2024

More Information

Terms related to this study

• Keywords: Healthy Male Subjects
• Other Study ID Numbers: 6356-009

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No