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NCT01149421 · ClinicalTrials.gov registry record · Phase 2

A Study of the Effect of LY2189265 on Blood Pressure and Heart Rate in Type 2 Diabetes

A Phase 2 study, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 2
Development phase
755
Enrollment target

NCT01149421: Completed Phase 2 study, sponsored by Eli Lilly and Company.

NCT01149421 is a Phase 2 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 755 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (468% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01149421, a Phase 2 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 2
Development phase
755 participants
Enrollment target

Study 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).

Primary Outcome

Mean 24-hour systolic blood pressure (SBP) was measured by using a 24-hour ambulatory blood pressure monitoring (ABPM) device attached to the participant's nondominant arm. Ambulatory blood pressure measurements were recorded every 20 minutes during the daytime (0700 to 2200 hours) and every 30 minutes during the nighttime hours (2200 to 0700), as preprogrammed into the device. For statistical analyses, diurnal hours were defined as 0800 to 2100 and nocturnal hours were defined as 0000 to 0600.

Interventions

  • DRUG Placebo
  • DRUG LY2189265

Trial Details

FieldValue
Enrollment Target 755 participants
Start Date 2010-06
Est. Completion 2012-01
Phase Phase 2
Eli Lilly and Company

1,341 total trials

What the finished NCT01149421 record still lists

NCT01149421 is an interventional study that assigns participants to a tested intervention. The registered 755 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (468% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT01149421 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01149421 about?

NCT01149421 is a clinical study titled "A Study of the Effect of LY2189265 on Blood Pressure and Heart Rate in Type 2 Diabetes". 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).

What is the current status of trial NCT01149421?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 755 participants. The study started on 2010-06. Estimated completion is 2012-01.

What interventions are being tested in trial NCT01149421?

The interventions under investigation include: Placebo (DRUG), LY2189265 (DRUG).

Who is sponsoring clinical trial NCT01149421?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01149421's enrollment target sits among peer trials

755 43rd of 2000 higher than 1,958 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01149421, the US trial registry maintained by the National Library of Medicine. NCT01149421 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.