Peking University First Hospital
Beijing, 100034, China
Location status: Recruiting
NCT Number: NCT07626515
This is a Phase I, randomized, double-blinded, placebo-controlled, study to assess the safety, tolerability, and pharmacokinetics (PK) of enicepatide in generally healthy adult Chinese participants with body mass index (BMI) ≥23.0 kilograms per meter squared (kg/m^2).
Interested in participating?
Request Info18 year–65 year
All sexes
Interventional
Phase 1
Beijing, 100034, China
Location status: Recruiting
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will receive enicepatide via subcutaneous (SC) injection as per the schedule in the protocol.
Other names: RO7795068, CT-388, RG6640
Participants will receive matching placebo via subcutaneous (SC) injection as per the schedule in the protocol.
Time frame: Baseline to Safety Follow-Up (27 weeks)
Time frame: Baseline to Safety Follow-Up (27 weeks)
Time frame: At prespecified time points from Baseline to Safety Follow-Up (27 weeks)
Time frame: At prespecified time points from Baseline to Safety Follow-Up (27 weeks)
Time frame: At prespecified time points from Baseline to Safety Follow-Up (27 weeks)
Time frame: At prespecified time points from Baseline to Safety Follow-Up (27 weeks)
Time frame: At prespecified time points from Baseline to Safety Follow-Up (27 weeks)
Time frame: At prespecified time points from Day 1 to Day 190
Time frame: At prespecified time points from Day 1 to Day 190
Time frame: At prespecified time points from Day 1 to Day 190
Time frame: At prespecified time points from Day 1 to Day 190
Time frame: At prespecified time points from Day 1 to Day 190
Time frame: Baseline through Week 24
Time frame: Baseline through Week 24
Contact information is provided by the study sponsor or research team.
Fastest response: use the inquiry form. https://www.gene.com/contact-us/submit-medical-inquiry
CONTACT
Reference Study ID Number: YP46402 https://forpatients.roche.com/ No attachments to email below.
CONTACT
888-662-6728 (U.S. Only)
Hoffmann-La Roche
Industry
A Phase I, Randomized, Double-Blinded, Placebo-Controlled, Study to Investigate the Safety, Tolerability, and Pharmacokinetics of Enicepatide in Adult Chinese Participants With Body Mass Index ≥23.0 kg/m2
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.
Published trials that share one or more normalized conditions with this study.
NCT07498270
Healthy Adult Participants, Healthy Participants
Madison, Wisconsin, United States
View Trial DetailsNCT07511205
Body Weight, Healthy Participants
Glendale, California, United States
View Trial DetailsNCT07219719
Healthy Participants
Madison, Wisconsin, United States
View Trial DetailsNCT07746167
Healthy Participants
Washington D.C., District of Columbia, United States
View Trial Details