A Phase 1 Study of S-1117

This is the first-in-human study of S-1117 designed to provide safety, tolerability, pharmacokinetic, and pharmacodynamic data in healthy volunteers.

This is a randomized, placebo-controlled, double-blind, study to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of S-1117 administered to healthy adult participants. This study will be conducted in two parts, Part 1 (single ascending dose, SAD) and Part 2 (multiple ascending doses, MAD).

Major Inclusion Criteria: 1. Is available for the entire duration of the study and follow up. 2. Is willing and able to comply with all study assessments and adhere to the protocol schedule and restrictions. 3. Voluntarily consents to participation in the trial as documented by signing the study informed consent form (ICF). 4. Has a body mass index (BMI) within 18 to 32 kg/m2, inclusive, and weighs ≥45 kg. 5. Is in good physical and mental health in the opinion of the Investigator or delegate. Major Exclusion Criteria: 1. Has a history of severe allergic or anaphylactic reaction as determined by the Investigator or delegate. 2. Is pregnant, nursing, or is planning to become pregnant or breastfeed during the trial. 3. Has a known immunodeficiency disorder. 4. Has a history of malignancy other than non-melanoma skin cancer. 5. Has a history of human immunodeficiency virus (HIV) or positive serology for HIV at Screening. 6. Has positive laboratory evidence for active hepatitis at screening. 7. Has received a live vaccine within 2 months of Screening. 8. Has any other condition or prior therapy that, in the opinion of the Investigator or delegate, may potentially compromise the safety or compliance of the participant, or may preclude the participant from successfully completing the study. Other inclusion/exclusion eligibility criteria apply.