Brenipatide
DrugAdministered SC
Other names: LY3537031
NCT Number: NCT07420283
The purpose of this study is to see if brenipatide, when compared to placebo, is safe and effective for participants with opioid use disorder, when used with buprenorphine with or without naloxone.
The maximum potential duration of study participation for a participant in Part A is approximately 144 weeks, maximum potential duration of study participation for a participant in Part B is approximately 116 weeks. The actual duration will vary for each participant depending on the time of enrollment and the overall rate of study enrollment.
Interested in participating?
Request Info18 year–75 year
All sexes
Interventional
Phase 2
CaRe Clinic, Calgary, Canada
The study consists of 2 parts, each with its own participant cohort
Participants will be enrolled in only one part of the study.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Note: any level of caffeine use is allowed
Administered SC
Other names: LY3537031
Administered SC
Administered sublingual or buccal
Time frame: Week 13 up to Week 24
Time frame: Week 13 up to Week 24
Time frame: Week 13 up to Week 24
Time frame: Week 13 up to Week 24
Time frame: Week 1 up to Week 24
Time frame: Baseline, Week 24
Time frame: Baseline, Week 24
Time frame: Baseline, Week 24
Time frame: Baseline, Week 24
Time frame: Baseline, Week 24
Time frame: Baseline, Week 24
Time frame: Baseline, Week 24
Time frame: Baseline, Week 24
Time frame: Baseline, Week 24
Time frame: Baseline up to Week 24
Time frame: Baseline up to Week 24
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 2, Randomized, Double-Blind, Placebo-Controlled Study With a Separate Open-label Cohort to Evaluate the Efficacy and Safety of Brenipatide as Adjunctive Treatment to Transmucosal Buprenorphine With or Without Naloxone in Early Recovery of Participants With Opioid Use Disorder (RENEW-Op-1)
Acronym: RENEW-Op-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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