Viewing Study NCT03407118


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Ignite Modification Date: 2026-03-01 @ 12:33 PM
Study NCT ID: NCT03407118
Status: COMPLETED
Last Update Posted: 2020-05-01
First Post: 2018-01-16
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: A Study of LY900014 in Japanese Participants With Type 1 Diabetes Mellitus
Sponsor: Eli Lilly and Company
Organization:

Study Overview

Official Title: Pharmacokinetics and Glucodynamics of LY900014 Compared to Insulin Lispro (Humalog) Following Single Dose Administration in Japanese Patients With Type 1 Diabetes Mellitus
Status: COMPLETED
Status Verified Date: 2018-08
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: This study will compare LY900014, a drug that lowers blood sugar, with insulin lispro (Humalog). Both drugs will be given by injection under the skin of the abdomen. This study will be conducted in participants with type 1 diabetes to investigate how quickly and how much LY900014 is absorbed and the effect of LY900014 on blood sugar levels in comparison with insulin lispro. The study will last about 3 to 6 weeks for each participant, not including screening.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
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?:

Secondary ID Infos

Secondary ID Type Domain Link View
I8B-MC-ITRZ OTHER Eli Lilly and Company View