A Study of S-892216-PO in Participants With Renal Impairment and Matched Controls
Not Applicable
Recruiting
- Conditions
- Renal Impairment
- Interventions
- Drug: S-892216-PO
- Registration Number
- NCT07217886
- Lead Sponsor
- Shionogi
- Brief Summary
The purpose of this study is to measure the pharmacokinetics, safety, and tolerability of S-892216 (S-892216-PO) in participants with mild, moderate, or severe renal impairment not on dialysis, or renal impairment requiring hemodialysis (HD), and in participants with normal renal function.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
- Considered to be healthy (for normal renal function participants) or medically stable (for participants with renal impairment), as determined by medical evaluation including medical history, physical examination, clinical laboratory tests, vital sign measurements, and 12-lead electrocardiogram during the screening period and on Day -1.
- Participants With Severe, Moderate, and Mild Renal Impairment not on HD (Group A, D and E): Participants that are not undergoing HD and have mild, moderate, or severe renal impairment based upon the 2021 Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) creatinine formula (estimated glomerular filtration rate [eGFR]) and the participant's body surface area (BSA) calculated at the screening visit.
- Participants With Renal Impairment Requiring HD (Group B): Receiving stable HD at least 3 times a week for at least 6 months prior to screening
- Participants With Normal Renal Function: Participants with clinical laboratory tests within normal reference range for the laboratory, or abnormal but considered not clinically significant by the investigator. Renal function, calculated by the 2021 CKD-EPI creatinine formula and the participant's BSA, must be normal (that is, eGFR ≥90 milliliters/minute).
Key
Exclusion Criteria
- Participants with life expectancy less than or equal to 3 months.
- History or presence of cardiovascular, respiratory, hepatic, gastrointestinal, endocrinological, hematological, or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs, constituting a risk when taking the study intervention, or interfering with the interpretation of data based on the judgment of the investigator.
- Participants With Normal Renal Function: History or presence of renal disorders capable of significantly altering the absorption, metabolism, or elimination of drugs, constituting a risk when taking the study intervention, or interfering with the interpretation of data.
- Participants With Any Renal Impairment (Groups A, B, D, and E): Participant with clinically significant laboratory values in the opinion of the investigator or outside protocol-specified ranges or limits during the screening period or on Day -1.
- Participants With Severe, Moderate, Mild Renal Impairment not on HD (Groups A, D, and E): Current or anticipated need for HD during the study.
Note: Other protocol-defined inclusion/exclusion criteria may apply.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Group A (Severe Renal Impairment) S-892216-PO Participants with severe renal impairment not on HD will receive S-892216-PO. Group C (Normal Renal Function) S-892216-PO Participants with normal renal function will receive S-892216-PO. Group B (Renal Impairment) S-892216-PO Participants with renal impairment requiring HD will receive S-892216-PO. Group D (Moderate Renal Impairment) S-892216-PO Participants with moderate impairment will receive S-892216-PO. Group D (Mild Renal Impairment) S-892216-PO Participants with mild impairment will receive S-892216-PO.
- Primary Outcome Measures
Name Time Method Group B Only: Cumulative Amount of the Drug Recovered in Dialysate (AHD) of S-892216 Day 1 (up to 6 hours postdose) Group B Only: Area Under the Dialysate Concentration in the Arterial Sides of Port-time Curve During Hemodialysis (AUChd) of S-892216 Day 1 (up to 6 hours postdose) Maximum Plasma Concentration (Cmax) of S-892216 Day 1 (predose up to 504 hours postdose) and Day 29 (predose up to 72 hours postdose) for Group B participants only Area Under the Plasma Concentration-time Curve From Time Zero to the Time of the Last Quantifiable Concentration After Dosing (AUC0-last) of S-892216 Day 1 (predose up to 504 hours postdose) and Day 29 (predose up to 72 hours postdose) for Group B participants only
- Secondary Outcome Measures
Name Time Method Number of Participants Experiencing Treatment-emergent Adverse Events (TEAEs) Day 1 through Day 39
Trial Locations
- Locations (4)
Orlando Clicinal Research Center
🇺🇸Orlando, Florida, United States
Global Clinical Professionals (GCP) LLC
🇺🇸St. Petersburg, Florida, United States
Genesis Clinical Research
🇺🇸Tampa, Florida, United States
Alliance for Multispecialty Research (AMR)-Knoxville
🇺🇸Knoxville, Tennessee, United States
Orlando Clicinal Research Center🇺🇸Orlando, Florida, United States