ECC5004 RBA FE Study in Healthy Participants
- Disease/Condition
- Type 2 Diabetes Mellitus
- Drug/Device/Intervention
- ECC5004
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- Eccogene
- Location
- Anaheim, United States of America
- Phase
- Phase 1
- Start date
- Feb 06, 2024
- End date
- Mar 30, 2024
- Enrollment
- 14 participants
ECC5004 PK parameters: AUC0-tlast,ECC5004 PK parameters: AUC0-inf,ECC5004 PK parameters: Cmax,ECC5004 PK parameters: tmax
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
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06268145
- Type
- Non-Device Trial
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.