ECC4703
Drugorally QD
NCT Number: NCT07505303
The primary objective of this trial is to evaluate the effect of oral ECC4703 on body weight reduction and in a sub-study on liver fat content as assessed by change in magnetic resonance imaging proton density fat fraction (MRI-PDFF) at Week 20.
This study is active but is not currently recruiting participants.
Notify Me18 year–75 year
All sexes
Interventional
Phase 2
Central Research Associates - Flourish - PPDS, Birmingham, Alabama, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
orally QD
orally QD
SC once weekly
Time frame: Baseline (Week 9) to Week 20
Time frame: Baseline (Week 9) to Week 20
Time frame: Baseline (Week 9) to Week 20
Time frame: Baseline (Week 9) to Week 20
Time frame: Baseline (Week 9) to Week 20
Time frame: Baseline (Week 9) to Week 20
Time frame: Baseline (Week 9) to Week 20
Time frame: Baseline (Week 9) to Week 20
Time frame: Baseline (Week 9) to Week 20
Change in HbA1c and fasting plasma glucose levels from baseline (Week 9) to Week 20
Time frame: Baseline (Week 9) to Week 20
Time frame: Baseline (Week 9) to Week 20
Time frame: Baseline (Week 9) to Week 20
Time frame: Baseline (Week 9) to Week 20
Time frame: Baseline (Week 9) to Week 20
Time frame: Baseline (Week 9) to Week 20
Time frame: Baseline (Week 9) to Week 20
Time frame: From first dose through Week 20 (or end of study visit)
Time frame: From first dose through Week 20 (or end of study visit)
Time frame: Baseline through Week 20
changes in clinical laboratory parameters, including hematology, serum chemistry, and urinalysis.
Time frame: Baseline through Week 20
Change in QT Interval, etc
Time frame: Baseline through Week 20
including blood pressure, etc
Time frame: Baseline through Week 20
including blood pressure, etc
Eccogene
Industry
A Phase 2a, Randomized, Double-blind, Placebo-controlled Trial to Evaluate the Efficacy, Safety, and Tolerability of ECC4703 as an Adjunct to Semaglutide in Adults With Obesity
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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