CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 388 enrolled
Drug / intervention
Insulin Peglispro +2 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01894568
NCT01894568Phase 3Completed

A Phase 3, Open Label, Randomized, Parallel, 26 Week Treatment Study Comparing LY2605541 With Insulin Glargine as Basal Insulin Treatment in Combination With Oral Anti Hyperglycemia Medications in Asian Insulin Naïve Patients With Type 2 Diabetes Mellitus

Eli Lilly and Company·interventional·Posted Jul 10, 2013·Updated Mar 15, 2019

In Brief

A Phase 3 clinical trial evaluating Insulin Peglispro, Insulin Glargine, and 1 other intervention for Type 2 Diabetes Mellitus. Completed, enrolled 388 participants across 31 sites in 3 countries.

Detailed Summary

The purpose of this study is to compare insulin peglispro (LY2605541) to insulin glargine in Asian insulin naïve participants who have been treated with oral anti hyperglycemia medications. Participants will receive 26 weeks of treatment.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesJapan, South Korea, Taiwan
Collaborators--

Timeline

Phase 3CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedJul 10, 2013
Enrollment StartJul 1, 2013
Primary CompletionApr 1, 2015
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 13.0 years ago

Interventions

Insulin Peglisprodrug

Administered SC using a prefilled pen.

Insulin Glarginedrug

Administered SC using a prefilled pen

Oral Antihyperglycemic Medications (OAMs)drug

Administered orally