Viewing Study NCT00127634



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Last Modification Date: 2024-10-26 @ 9:13 AM
Study NCT ID: NCT00127634
Status: COMPLETED
Last Update Posted: 2018-03-09
First Post: 2005-08-04

Brief Title: Study of Human Insulin Inhalation Powder in Patients With Type 1 Diabetes
Sponsor: Eli Lilly and Company
Organization: Eli Lilly and Company

Study Overview

Official Title: A Pivotal Long-Term Open-Label Parallel Study of the Efficacy and Safety of Human Insulin Inhalation Powder in Patients With Type 1 Diabetes Mellitus
Status: COMPLETED
Status Verified Date: 2018-03
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 is a phase 3 open-label randomized study to evaluate the safety and efficacy of the LillyAlkermes inhaled insulin system compared to injected pre-meal insulin in non-smoking patients with type 1 diabetes Patients will be treated for 24 months with a 2-month follow-up period
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
H7U-MC-IDAH None None None