Viewing Study NCT01640834


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Study NCT ID: NCT01640834
Status: COMPLETED
Last Update Posted: 2018-10-29
First Post: 2012-07-12
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: Study of LY2409021 in Participants With Type 1 Diabetes
Sponsor: Eli Lilly and Company
Organization:

Study Overview

Official Title: Pilot Study of the Effects of LY2409021 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 study involves taking a single dose of 100 milligrams (mg) or 300 mg LY2409021 or placebo (an inactive medicine) taken as up to 3 capsules by mouth. The study will evaluate if this drug will reduce the amount of insulin a type 1 diabetic needs over 24 hours. This study includes a 7-day hospitalization period at the clinical research unit (CRU) and will involve screening within 30 days of the start of the study as well as telephone consultations within 5 days after discharge from the CRU.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
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?:

Secondary ID Infos

Secondary ID Type Domain Link View
I1R-MC-GLBR OTHER Eli Lilly and Company View
2011-006178-19 EUDRACT_NUMBER None View