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RECRUITING
NCT07205432
PHASE1

Phase I Study of XTL6001 Injection in Healthy and Obese Subjects

Sponsor: Shanghai Xitaili Biomedicine Technology co., Ltd.

View on ClinicalTrials.gov

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

DRUG

XTL6001

XTL6001 is a triple-target Glucagon-like peptide-1 receptor (GLP-1R) relevant agonist, intending to manage overweight/obesity and other metabolic diseases

DRUG

Placebo

This intervention contains no active ingredients

Locations (1)

Beijing Shijitan Hospital, Capital Medical University

Beijing, Beijing Municipality, China