Viewing Study NCT03555305


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Study NCT ID: NCT03555305
Status: COMPLETED
Last Update Posted: 2020-11-24
First Post: 2018-06-01
Is NOT Gene Therapy: False
Has Adverse Events: True

Brief Title: A Study of Insulin Glargine (LY2963016) in Healthy Chinese Participants
Sponsor: Eli Lilly and Company
Organization:

Study Overview

Official Title: Relative Bioavailability of LY2963016 to LANTUSĀ® After Single-Dose Subcutaneous Administration in Healthy Chinese Subjects
Status: COMPLETED
Status Verified Date: 2019-11-15
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 purpose of this study is to compare a study drug known as Insulin glargine with Lantus in healthy Chinese participants. Blood samples will be taken to compare how the body handles the drugs and how they affect blood sugar levels. Side effects and tolerability will be documented. The study will last at least 18 days, not including screening. Screening is required within 4 weeks prior to the start of the study.
Detailed Description: None

Study Oversight

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

Secondary ID Infos

Secondary ID Type Domain Link View
I4L-MC-ABEF OTHER Eli Lilly and Company View