LY3537031
DrugAdministered SC
Other names: Brenipatide
NCT Number: NCT07219966
The purpose of this study is to see if brenipatide when compared to a placebo works and is safe for participants with moderate-to-severe Alcohol Use Disorder (AUD). Participation in this study will last approximately 56 weeks.
Interested in participating?
Request Info18 year–75 year
All sexes
Interventional
Phase 3
ANIMA Research, Diepenbeek, Belgium
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Administered SC
Other names: Brenipatide
Administered SC
Time frame: Up to 56 weeks
Time frame: Up to 56 weeks
Time frame: Baseline up to Week 56
Time frame: Baseline up to Week 56
Time frame: Baseline up to Week 56
Time frame: Baseline up to Week 56
Time frame: Baseline up to Week 56
Time frame: Baseline up to Week 56
Contact information is provided by the study sponsor or research team.
Physicians interested in becoming principal investigators please contact
CONTACT
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or
CONTACT
Eli Lilly and Company
Industry
A Phase 3, Multicenter, Randomized, Double-Blind Study to Investigate the Efficacy and Safety of Brenipatide Compared With Placebo for the Treatment of Adult Participants With Moderate-to-Severe Alcohol Use Disorder (RENEW-ALC-1)
Acronym: RENEW-ALC-1
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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