A Study to Evaluate the Effect of Severe Renal Impairment on the Single-dose Pharmacokinetics of Odalasvir

Inclusion Criteria

• •Cohorts 1 and 2:
• •Participant must have a body mass index (BMI; weight in kilogram (kg) divided by the square of height in meters) of 18 to 36 kilogram per meter square (kg/m\^2), extremes included, and a body weight not less than 50.0 kg
• •Participant must be willing and able to adhere to the prohibitions and restrictions specified in the protocol
• •Male Participant must agree not to donate sperm from enrollment (Day 1) in the study until at least 30 days after receiving the study drug
• •Female Participant, except if postmenopausal, must have a negative serum (beta human chorionic gonadotropin \[beta hCG\]) pregnancy test at screening and negative highly sensitive urine pregnancy test at Day -1
• •Cohort 1:
• •Participant must have severe renal impairment not requiring dialysis, defined as an estimated glomerular filtration rate (eGFR) less than (\<) 30 milliLiter per minute (mL/min)/1.73 m\^2
• •Participant must have stable renal function that is no significant change in renal function as evidenced by the (mean) screening serum creatinine value within +/-25 percent (%) from the determination obtained at least 3 months prior to screening, and expected to remain stable during the study, and not be planning to initiate dialysis during the study period
• •Participant must be otherwise healthy except for renal impairment and its underlying disease states and mild comorbidities and participant must be medically stable on the basis of physical examination, medical history, vital signs, 12-lead electrocardiogram (ECG), and clinical laboratory tests performed at screening. If there are abnormalities or results outside the normal reference ranges, the participant may be included only if the investigator judges the abnormalities or deviations from normal to be not clinically significant or to be appropriate and reasonable for the population under study. This determination must be recorded in the participant's source documents and initialed by the investigator
• •Cohort 2:
• •Participant must be healthy on the basis of physical examination, medical history, vital signs, 12-lead ECG, and clinical laboratory tests performed at screening
• •Participant must have an eGFR greater than or equal to (\>=) 90 mL/min/1.73 m\^2