A Study of LY3549492 in Participants With Type 2 Diabetes Mellitus (T2DM)
NCT05327595 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 80
Last updated 2024-05-30
Summary
The main purpose of this study is to evaluate the safety and tolerability of LY3549492 in participants with T2DM. Blood tests will be done to check how much LY3549492 gets into the bloodstream and how the body handles LY3549492. This study has two parts. Each participant will enroll in only one part. The study will last either 12 or 13 weeks, depending on part.
Conditions
- Diabetes Mellitus, Type 2
Interventions
- DRUG
-
LY3549492
Administered orally.
- DRUG
-
Administered orally.
- DRUG
-
Administered orally.
- DRUG
-
Midazolam
Administered orally.
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST) · Eli Lilly and Company
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-05-09
- Primary Completion
- 2024-04-22
- Completion
- 2024-04-22
- FDA Drug
- Yes
Countries
- Germany
Study Locations
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