A Phase 1, Open-label, Single-Ascending Dose and Multiple-Ascending Dose Study to Investigate the Safety and Tolerability of TE-8105 Administered Subcutaneously in Overweight/Obese Participants Without Diabetes
This is a Phase 1, first-in-human, prospective, open-label study to evaluate the safety, tolerability, PK, and PD of TE-8105 in overweight/obese participants without diabetes. Study TE-8105-101 consists of 2 parts: Part A (single-ascending dose [SAD]) and Part B (multiple-ascending dose [MAD]).