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Starting soon Phase 1

A Study to Learn How Different Forms of the Study Medicine Called Berobenatide is Taken up Into the Blood in Adults With Overweight or Obesity

NCT07876531 · tracked via the Priya Life Science USA tracker
Sponsor
Phase
Phase 1
Started
2026-10-16
Last updated
2026-10-15

Condition(s) studied

Overweight and/or ObesityHealthy Participants

Investigational drug(s) / intervention(s)

Berobenatide →

Berobenatide: Solution for Injection

Study summary

This is a single dose study to learn how safe and effective the study medicine is using different delivery systems for adults with overweight or obesity. Overweight or obesity means having more body fat than what is healthy.

The study involves multiple clinic visits at a study site over the length of the study.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Key Inclusion Criteria: * Participants 18 years of age or older * BMI of 27-45 kg/m2; and a total body weight \>50 kg (110 lb) Key Exclusion Criteria: * Pregnant or breastfeeding women, or those planning pregnancy during the study * History of other chronic disorders * Personal or first-degree family history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia type 2 (MEN2), or suspected MTC * Clinically significant gastric emptying abnormality or chronically taking drugs that directly affect gastrointestinal (GI) motility * Acute GI symptoms at screening, Day -1, or prior to administration of study intervention

Primary outcome measure(s)

  • Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve (AUC) of Berobenatide — Up to 85 days
  • PK: Maximum Observed Concentration (Cmax) of Berobenatide — Up to 85 days

Trial sites (1)

FacilityCityRegionStatus
Anaheim Clinical Trials, LLC Anaheim California
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07876531 on ClinicalTrials.gov ↗ ← All trials in the USA