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First in Human Study in Subjects With Obesity, But Otherwise Healthy

Obesity Clinical Trial

Official title:
A Phase 1, Randomized, Placebo-Controlled, Double-Blind First in Human, Single and Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of DA-1726 in Participants With Obesity.

Clinical Trial Summary

This is a First in Human study to evaluate the safety and tolerability of DA-1726 following single and multiple doses in participants with obesity, but otherwise healthy subjects.

Clinical Trial Description

This is a Phase 1, randomized, placebo-controlled, double-blind, sequential parallel group study to investigate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of single and multiple ascending doses of DA-1726 in adult participants (aged 18 to 65 years) with obesity (BMI ≥30 - 45 kg/m2). DA-1726 will be administered via subcutaneous (SC) injection within the clinic setting. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06252220
Study type Interventional
Source NeuroBo Pharmaceuticals Inc.
Contact Robert Homolka, MS
Phone 8572991038
Email CRinfo@Neurobopharma.com
Status Recruiting
Phase Phase 1
Start date March 25, 2024
Completion date June 2025
View Details
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