Viewing Study NCT03890003


Ignite Creation Date: 2025-12-24 @ 7:30 PM
Ignite Modification Date: 2025-12-25 @ 5:12 PM
Study NCT ID: NCT03890003
Status: COMPLETED
Last Update Posted: 2019-06-05
First Post: 2019-03-22
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: A Study of an Automated Insulin Delivery System in Adult Participants With Type 1 Diabetes
Sponsor: Eli Lilly and Company
Organization:

Study Overview

Official Title: An Early Feasibility Study to Evaluate the Predictive Low Glucose Suspend Functionality and Safety in an Automated Insulin Delivery System in Adult Patients With Type 1 Diabetes Mellitus
Status: COMPLETED
Status Verified Date: 2019-06-01
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 early feasibility study is to assess the predictive low glucose suspend (PLGS) feature's safety, functionality and performance.
Detailed Description: None

Study Oversight

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

Secondary ID Infos

Secondary ID Type Domain Link View
F3Z-MC-IORC OTHER Eli Lilly and Company View