A Study of LY3451838 in Healthy Participants
NCT03692949 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 53
Last updated 2025-09-11
Summary
The study has two parts. In Part A, single increasing doses of LY3451838 will be administered intravenously (into a vein). In Part B, a single dose of LY3451838 will be administered subcutaneously (just under the skin).
Conditions
- Healthy
Interventions
- DRUG
-
LY3451838
Administered IV Part A
- DRUG
-
LY3451838
Administered IV Part A
- DRUG
-
LY3451838
Administered IV Part A
- DRUG
-
LY3451838
Administered IV Part A
- DRUG
-
LY3451838
Administered IV Part A
- DRUG
-
LY3451838
Administered IV Part A
- DRUG
-
LY3451838
Administered SC Part B
- DRUG
-
Administered IV in Part A and SC in Part B
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
- BASIC_SCIENCE
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 21 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2018-12-11
- Primary Completion
- 2020-02-26
- Completion
- 2020-02-26
Countries
- Singapore
Study Locations
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