Viewing Study NCT06557356


Ignite Creation Date: 2025-12-24 @ 11:36 PM
Ignite Modification Date: 2026-01-02 @ 1:57 PM
Study NCT ID: NCT06557356
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2025-11-20
First Post: 2024-08-14
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: A Study of LY3532226 in Participants With Obesity
Sponsor: Eli Lilly and Company
Organization:

Study Overview

Official Title: A Dose-Escalation Phase 1, Investigator- and Participant-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Multiple Doses of LY3532226 in Participants With Obesity
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2025-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The main purpose of this study is to evaluate the safety and tolerability of the study drug known as LY3532226 in participants with obesity. Blood tests will be performed to check how much LY3532226 gets into the bloodstream and how long it takes the body to eliminate it following weekly or monthly administration. Part A of the study will last approximately 16 weeks, excluding screening period. Part B of the study will last approximately 20 weeks, excluding the screening period. Part C of the study will last approximately 8 weeks, excluding the screening period.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
J2V-MC-GZLD OTHER Eli Lilly and Company View