CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 755 enrolled
Drug / intervention
LY2189265 +1 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/NCT01149421
NCT01149421Phase 2Completed

The Effect of LY2189265 on Blood Pressure and Heart Rate, as Assessed by Ambulatory Blood Pressure Monitoring, in Patients With Type 2 Diabetes Mellitus

Eli Lilly and Company·interventional·Posted Jun 23, 2010·Updated Feb 2, 2015

In Brief

A Phase 2 clinical trial evaluating LY2189265 and Placebo for Diabetes Mellitus, Type 2. Completed, enrolled 755 participants across 76 sites in 8 countries.

Detailed Summary

The purpose of this study is to assess the effects of 2 doses of LY2189265 on blood pressure and heart rate using 24-hour ambulatory blood pressure monitoring (ABPM), in participants with type 2 diabetes mellitus treated with oral antihyperglycemic medications (OAMs).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesArgentina, Brazil, Canada, Czechia, Denmark, India, Puerto Rico, United States
Collaborators--

Timeline

Phase 2CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedJun 23, 2010
Enrollment StartJun 1, 2010
Primary CompletionSep 1, 2011
Study CompletionJan 1, 2012
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 16.0 years ago

Interventions

LY2189265drug

Administered as a subcutaneous injection once weekly for 26 weeks

Placebodrug

Administered as a subcutaneous injection once weekly for 26 weeks