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CompletedNCT07307638

Dose-escalation and Food Effect Study of ZT006 in Healthy, Overweight and Obese Participants

A Randomized, Double-blind, Placebo-controlled, Dose-escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single and Multiple Doses of ZT006 as Well as the Food Effect on the Pharmacokinetics of ZT006 in Healthy, Overweight and Obese Participants

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
94 (actual)
Sponsor
Beijing QL Biopharmaceutical Co.,Ltd · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

ZT006 is an oral, long-acting glucagon-like peptide-1. This first-in-human study is designed to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of ZT006 in healthy, overweight and obese participants. The study comprises three parts, i.e. single dose-escalation, multiple dose-escalation, food effect on the pharmacokinetics of ZT006. In the single dose-escalation study, participants will receive a single dose (ZT006 dose level 1 - 5 or corresponding placebo) of ZT006 under fasted condition. A higher dose can only be given after obtaining acceptable safety and tolerability data for at least 7 days after the previous dose. After study drug administration, there will be a 7-day in-house period for safety observation and pharmacokinetics samples collection. Participants will join ambulatory visits until 42 days post-dose. In the multiple dose-escalation study, participants will receive a daily dose of ZT006 or corresponding placebo over 42 days in a dose up-titration fashion according to the following regimen: * Cohort 1: dose level 1 - dose level 2 - dose level 3 * Cohort 2: dose level 1 - dose level 2 - dose level 3 - dose level 4 * Cohort 3: dose level 2 - dose level 3 - dose level 4 * Cohort 4: dose level 2 - dose level 3 - dose level 4 - dose level 5 Dosing of a cohort with higher drug exposure can only be done after evaluation of safety and tolerability data for at least 14 days after the first dose in the previous cohort. Participants will join ambulatory visits until 35 days after the last dose. To evaluate the food effect on the pharmacokinetics of ZT006, participants who have received single dose of ZT006 or placebo of dose level 4 in the single dose-escalation study will receive another dose of ZT006 or placebo after a high fat, high caloric breakfast.

Conditions

Interventions

TypeNameDescription
DRUGZT006Participants will receive a single dose of ZT006 of dose level 1 under fasted condition.
DRUGZT006Participants will receive a single dose of ZT006 of dose level 2 under fasted condition.
DRUGZT006Participants will receive a single dose of ZT006 of dose level 3 under fasted condition.
DRUGZT006Participants will receive a single dose of ZT006 of dose level 4 under fasted condition in period 1, and after a high fat, high caloric breakfast in period 2.
DRUGZT006Participants will receive a single dose of ZT006 of dose level 5 under fasted condition.
DRUGZT006Participants will receive daily doses of ZT006 for 42 days: dose level 1 for 7 days, then dose level 2 for 7 days, then dose level 3 for 28 days.
DRUGZT006Participants will receive daily doses of ZT006 for 42 days: dose level 1 for 7 days, then dose level 2 for 7 days, then dose level 3 for 14 days, then dose level 4 for 14 days.
DRUGZT006Participants will receive daily doses of ZT006 for 42 days: dose level 2 for 7 days, then dose level 3 for 7 days, then dose level 4 for 28 days.
DRUGZT006Participants will receive daily doses of ZT006 for 42 days: dose level 2 for 7 days, then dose level 3 for 7 days, then dose level 4 for 14 days, then dose level 5 for 14 days.
DRUGPlacebo of ZT006Participants will receive a single dose of placebo of ZT006 under fasted condition.
DRUGPlacebo of ZT006Participants will receive a single dose of placebo of ZT006 under fasted condition in period 1, and after a high fat, high caloric breakfast in period 2.
DRUGPlacebo of ZT006Participants will receive daily doses of placebo of ZT006 for 42 days.

Timeline

Start date
2024-11-28
Primary completion
2025-06-14
Completion
2025-06-24
First posted
2025-12-29
Last updated
2025-12-29

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07307638. Inclusion in this directory is not an endorsement.