A Study of Food Effect and Esomeprazole on LY4064809 in Healthy Adult Participants
NCT06991179 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 36
Last updated 2025-09-23
Summary
The purpose of this study is to evaluate the safety and effect of food on LY4064809 and the safety and effect of stomach changes by a proton pump inhibitor (PPI) esomeprazole, under fasted conditions in healthy adult participants. Blood tests will be performed to investigate how the body processes the study drug and how the study drug affects the body.
Conditions
- Healthy
Interventions
- DRUG
-
LY4064809
Administered orally
Sponsors & Collaborators
-
Scorpion Therapeutics, a wholly owned subsidiary of Eli Lilly and Company
lead INDUSTRY
Principal Investigators
-
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
- NONE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Max Age
- 55 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2025-05-20
- Primary Completion
- 2025-09-02
- Completion
- 2025-09-02
- FDA Drug
- Yes
Countries
- United States
Study Locations
More Related Trials
-
A Trial to Evaluate the Effect of Esomeprazole on the Pharmacokinetics of Emraclidine in Healthy Adult Participants
NCT06366243 ·Status: COMPLETED ·Phase: PHASE1
-
A Study in Healthy Men to Test Whether Esomeprazole Influences the Amount of BI 3000202 in the Blood
NCT06419660 ·Status: COMPLETED ·Phase: PHASE1
-
A Multicenter, Randomized, Double-Blind Parallel-Group, Placebo-Controlled Efficacy Study Comparing 4 Weeks of Treatment With Esomeprazole 20 mg Once Daily to Placebo qd for the Resolution of Upper Abdominal Pain in Patients With Symptomatic Gastroesophageal Reflux Disease (sGERD)
NCT00626535 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Test Bioavailability of of 2 New Formulations of UCB0599 in Healthy Participants in Part A and to Test Safety, Tolerability, and Pharmacokinetic (PK) of UCB0599 in Healthy Japanese and Chinese Participants in Part B
NCT05845645 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Assess the Levels in Blood Plasma of BMS-986278 in Healthy Participants Following Administration of Tablets, With or Without Food, and in the Presence of an Antacid (Esomeprazole)
NCT04468815 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of the Effects of Multiple Doses of Dexlansoprazole, Lansoprazole, Omeprazole or Esomeprazole on the Pharmacokinetics and Pharmacodynamics of Clopidogrel in Healthy Participants.
NCT00942175 ·Status: COMPLETED ·Phase: PHASE1
-
Barrett's Esophagus - 315 - 3 Way Cross-Over
NCT00637559 ·Status: COMPLETED ·Phase: PHASE4
-
Food Interaction Study To Assess the Effect of Food on the Pharmacokinetics of Esomeprazole 20 mg/Acetylsalicylic Acid 81 mg
NCT01163630 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Determine the Relative Bioavailability of Capsule and Tablet Formulations of GDC-0941 and the Effect of Food and Proton Pump Inhibition on GDC-0941 Tablet Pharmacokinetics in Healthy Volunteers
NCT00999128 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Esomeprazole in Healthy Adult Subjects Under Fasting Condition
NCT05235217 ·Status: COMPLETED ·Phase: PHASE1
-
PPI And Food Effect Study For PF-06463922 In Healthy Volunteers
NCT02569554 ·Status: COMPLETED ·Phase: PHASE1
-
Efficacy of Esomeprazole in Patients With Frequent Heartburn
NCT01370525 ·Status: COMPLETED ·Phase: PHASE3
-
Effect of Esomeprazole 40 mg.Daily for 7 Days on Acid Reflux and Related Arousals During Sleep in Patients With GERD
NCT01089959 ·Status: UNKNOWN ·Phase: PHASE2/PHASE3
-
Study Comparing the Effects of Esomeprazole Adminstered Orally and Intravenously on Basal and Pentrigastrin-stimulated Acid Output in Subjects With Symptoms of Gastroesophageal Reflux Disease (GERD)
NCT00625495 ·Status: COMPLETED ·Phase: PHASE4
-
A Study to Investigate the Relative Bioavailability of 2 Different Formulations of AZD4144, the Effect of Food and Omeprazole on the Pharmacokinetics of AZD4144 in Healthy Participants
NCT06948006 ·Status: COMPLETED ·Phase: PHASE1
-
An Open, Randomized, Two Way Crossover Study Comparing the Effect of 20mg Esomeprazole Administered Orally and Intravenously as a 15 Minute Infusion on Basal and Pentagastrin-Stimulated Acid Output in Subjects With Symptoms of Gastroesophageal Reflux Disease (GERD)
NCT00629564 ·Status: COMPLETED ·Phase: PHASE4
-
PK Study to Evaluate Esomeprazole Plasma Levels Following Administration of PN 400
NCT00599404 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Evaluate the Effect of Food, Formulation, and a Proton Pump Inhibitor (PPI) on Calderasib (MK-1084) in Healthy Adult Participants (MK-1084-003)
NCT06619314 ·Status: COMPLETED ·Phase: PHASE1
-
BE of Torrent's Esomeprazole Mg DR Capsules
NCT02680119 ·Status: COMPLETED ·Phase: PHASE1
-
An Open Label pH Comparison of Esomeprazole and Lansoprazole in Barrett's Esophagus Patients
NCT00352261 ·Status: COMPLETED ·Phase: PHASE4
-
A Study to Examine the Effects of Esomeprazole on the Pharmacokinetics of Orally Administered Lapatinib in Subjects With Metastatic ErbB2 Positive Breast Cancer
NCT00849329 ·Status: COMPLETED ·Phase: PHASE1
-
Relative Bioavailability and Drug-drug Interaction Study With MT-7117 and a Proton Pump Inhibitor
NCT03688022 ·Status: COMPLETED ·Phase: PHASE1
-
A 3-Part Study to Determine the Relative Bioavailability of Capsule and Tablet Formulations of GDC-0980, the Effect of Food, and the Effect of Rabeprazole on the Pharmacokinetics of the Tablet
NCT01287091 ·Status: COMPLETED ·Phase: PHASE1
-
Study to Determine the Single and Repeat Dose Pharmacokinetics, Food Effect, Proton Pump Inhibitor (PPI) Drug Interaction, Safety and Tolerability of Oral Prototype Formulations of BOS172767 in Healthy Subjects
NCT03464058 ·Status: COMPLETED ·Phase: PHASE1
-
Evaluating the Effects of Omeprazole on the Pharmacokinetics of XS004 (Dasatinib) Tablets in Healthy Adult Subjects Under Fasting Conditions
NCT05433896 ·Status: COMPLETED ·Phase: PHASE1