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NCT04644809

A Study of LY3561774 in Participants With Dyslipidemia

Completed Phase 1 Last updated 10 August 2022
What this trial tests

Phase 1 trial testing LY3561774 in Dyslipidemias in 74 participants. Completed in 17 May 2022.

Timeline
30 November 2020
Primary endpoint
17 May 2022
17 May 2022

Quick facts

Lead sponsorEli Lilly and Company
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designsequential
Maskingdouble
Primary purposebasic science
Enrollment74
Start date30 November 2020
Primary completion17 May 2022
Estimated completion17 May 2022
Sites5 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Eli Lilly and Company — full company profile →

Who can join

Adults 18 to 65, any sex, with Dyslipidemias. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a 3-part study. In Parts A and B, the main purpose is to evaluate the safety and tolerability of the study drug known as LY3561774 in participants with dyslipidemia (high blood fat levels). How the body processes the study drug and the effect of the study drug on blood fat levels will also be investigated. Part C will mainly evaluate the safety and tolerability of LY3561774 as well as how the body processes the study drug in Japanese participants. The study may last up 52, 56 and 28 weeks for each participant in Parts A, B and C, respectively. There are up to 22, 26 and 16 visits in Parts A, B and C, respectively.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of LY3561774

Trials testing the same drug.

Other recruiting trials for Dyslipidemias

Currently open trials in the same condition.

Other Eli Lilly and Company trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04644809.

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