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ACTIVE NOT RECRUITING
NCT06916143
PHASE1

Comparing the Extent to Which Three Different Formulations of LY4100511 (DC-853) Are Made Available in the Body, Alone and in the Presence of a Drug That Reduces Stomach Acid

Sponsor: Eli Lilly and Company

View on ClinicalTrials.gov

Summary

The main purpose of this study is to compare the bioavailability of 3 different formulations of LY4100511 and if the use of a proton pump inhibitor (PPI) alters the bioavailability of the 3 different formulations.

Official title: A Phase 1, Open-label, Randomized, Four-way Crossover Study to Assess the Relative Bioavailability of Two Phase 3 LY4100511 (DC-853) Tablet Formulations Compared With the Phase 2 LY4100511(DC-853) Tablet Formulation, With and Without a Proton Pump Inhibitor in Healthy Participants

Key Details

Gender

All

Age Range

18 Years - 55 Years

Study Type

INTERVENTIONAL

Enrollment

48

Start Date

2025-04-08

Completion Date

2026-07

Last Updated

2026-04-01

Healthy Volunteers

Yes

Interventions

DRUG

LY4100511

Administered orally.

DRUG

Rabeprazole

Administered orally.

Locations (2)

Clinical Pharmacology of Miami

Miami, Florida, United States

Alliance for Multispecialty Research, LLC

Knoxville, Tennessee, United States