CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 24 enrolled
Drug / intervention
Lebrikizumab +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06243198
NCT06243198Phase 1Completed

A Phase 1, Participant- and Investigator-blinded, Randomized, Single-dose Study to Investigate the Safety and Pharmacokinetics of Lebrikizumab in Healthy Chinese Participants

Eli Lilly and Company·interventional·Posted Feb 6, 2024·Updated Sep 12, 2025

In Brief

A Phase 1 clinical trial evaluating Lebrikizumab and Placebo for Healthy. Completed, enrolled 24 participants across 1 site.

Detailed Summary

The main purpose of this study is to determine the tolerability and side effects related to lebrikizumab comparing with placebo given as a single dose administered under the skin to healthy Chinese participants. The study will also assess how fast lebrikizumab gets into the blood stream and how long the body takes to get rid of it. Each enrolled participant will receive a single dose of either Lebrikizumab or placebo. For each participant, the total duration of the study will be approximately up to 21 weeks, including screening period.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy
CountriesChina
Collaborators--

Timeline

Phase 1CompletedFinished
202420252026
First PostedFeb 6, 2024
Enrollment StartMar 28, 2024
Primary CompletionSep 3, 2024
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 2.4 years ago

Interventions

Lebrikizumabdrug

Administered subcutaneously (SC)

Placebodrug

Administered subcutaneously (SC)