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Phase I Study of XTL6001 Injection in Healthy and Obese Subjects
Sponsor: Shanghai Xitaili Biomedicine Technology co., Ltd.
Summary
This is a multicenter, randomized, double-blind, placebo-controlled Phase I study to evaluate safety, PK and PD of single ascending dose (SAD) and multiple ascending dose (MAD) of XTL6001 injection in healthy and obese adult subjects. SAD study: Includes 5 dose cohorts, with 40 subjects planned for enrollment. MAD study Includes 2 dose cohorts, with 30 subjects planned for enrollment.
Official title: A Randomized, Double-blind, Placebo-controlled Phase I Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) Administration of XTL6001 Injection in Healthy and Obese Subjects
Key Details
Gender
All
Age Range
18 Years - 65 Years
Study Type
INTERVENTIONAL
Enrollment
80
Start Date
2025-06-13
Completion Date
2026-04
Last Updated
2025-10-03
Healthy Volunteers
Yes
Interventions
XTL6001
XTL6001 is a triple-target Glucagon-like peptide-1 receptor (GLP-1R) relevant agonist, intending to manage overweight/obesity and other metabolic diseases
Placebo
This intervention contains no active ingredients
Locations (1)
Beijing Shijitan Hospital, Capital Medical University
Beijing, Beijing Municipality, China