Viewing Study NCT06352892



Ignite Creation Date: 2024-05-06 @ 8:22 PM
Last Modification Date: 2024-10-26 @ 3:26 PM
Study NCT ID: NCT06352892
Status: COMPLETED
Last Update Posted: 2024-05-29
First Post: 2024-04-03

Brief Title: A Study to Evaluate AMG 133 in Chinese Participants With Obesity or Overweight
Sponsor: Amgen
Organization: Amgen

Study Overview

Official Title: A Phase 1 Open-label Randomized Parallel-group Single-dose Study to Evaluate the Pharmacokinetics Safety and Tolerability of AMG 133 Administered Subcutaneously in Chinese Subjects With Obesity or Overweight
Status: COMPLETED
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The main objective of the study is to assess the pharmacokinetics PK of Maridebart Cafraglutide after a single subcutaneous SC administration in overweight or obese Chinese participants
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: True
Is an FDA AA801 Violation?: None