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NCT06268145Recruiting

ECC5004 RBA FE Study in Healthy Participants

An Open-Label, Randomized, Single Dose, Crossover Clinical Study to Assess the Relative Bioavailability of Current Tablet Formulation (F1) Compared to New Tablet Formulation (F2) of ECC5004 and Food Effects on F1 and F2 of ECC5004 in Healthy Participants
EccogenePhase 1ClinicalTrials.govdrug
Study focus
Drug/Device/Intervention
ECC5004
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Eccogene
Location
Anaheim, United States of America
Timeline & enrollment
Phase
Phase 1
Start date
Feb 06, 2024
End date
Mar 30, 2024
Enrollment
14 participants
Primary outcome

ECC5004 PK parameters: AUC0-tlast,ECC5004 PK parameters: AUC0-inf,ECC5004 PK parameters: Cmax,ECC5004 PK parameters: tmax

Summary

This study is a Phase 1, open-label, randomized, single dose, fixed sequence, crossover study
 designed to compare the relative bioavailability of 50 mg ECC5004 current tablet formulation
 (F1) and 50 mg ECC5004 new tablet formulation (F2) under fasted and fed conditions in healthy
 participants

ICD-10 classifications
Type 2 diabetes mellitusType 2 diabetes mellitus with unspecified complicationsType 2 diabetes mellitus with other specified complicationsType 2 diabetes mellitus without complicationsType 2 diabetes mellitus with multiple complications
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06268145
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06268145 through Pure Global AI's free database. This Phase 1 trial is sponsored by Eccogene and is currently Recruiting. The study focuses on Type 2 Diabetes Mellitus. Target enrollment is 14 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.