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NCT01263197 · ClinicalTrials.gov registry record · Phase 1
A Study of LY2216684 in Healthy Participants Receiving Albuterol or Propanolol
A Phase 1 study of Major Depressive Disorder, sponsored by Eli Lilly and Company.
- Completed
- Registry status
- Phase 1
- Development phase
- 48
- Enrollment target
- 1
- Study location
NCT01263197 is a Phase 1 study of Major Depressive Disorder that has completed, run by Eli Lilly and Company. The registered enrollment target is 48 participants, below the 377-participant average among 282 other Major Depressive Disorder trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01263197, a Phase 1 study of Major Depressive Disorder, has completed, sponsored by Eli Lilly and Company.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 48 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine the effect of LY2216684 on heart rate of participants receiving Albuterol and Propranolol. Information about any side effects that may occur will also be collected.
Conditions Studied
Interventions
- DRUG propranolol
- DRUG LY2216684
- DRUG albuterol
- DRUG placebo for LY2216684
- DRUG placebo for albuterol
Study Locations (1)
Indiana
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. - Evansville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 48 participants |
| Start Date | 2010-12 |
| Est. Completion | 2011-03 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01263197
The ClinicalTrials.gov registry entry for NCT01263197 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 48 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 377-participant average among 282 other Major Depressive Disorder trials with a reported enrollment target (87% lower). The listed sponsor is Eli Lilly and Company, which has 1,341 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Major Depressive Disorder appearing as the primary indexed condition, and to 5 interventions - of which propranolol is the first listed.
NCT01263197 reports 1 study location spanning 1 distinct geographic area - top geographies include Indiana.
Frequently Asked Questions
What is clinical trial NCT01263197 about?
NCT01263197 is a clinical study titled "A Study of LY2216684 in Healthy Participants Receiving Albuterol or Propanolol". The purpose of this study is to determine the effect of LY2216684 on heart rate of participants receiving Albuterol and Propranolol. Information about any side effects that may occur will also be collected.
What is the current status of trial NCT01263197?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 48 participants. The study started on 2010-12. Estimated completion is 2011-03.
What conditions does trial NCT01263197 study?
This clinical trial studies the following conditions: Major Depressive Disorder.
What interventions are being tested in trial NCT01263197?
The interventions under investigation include: propranolol (DRUG), LY2216684 (DRUG), albuterol (DRUG), placebo for LY2216684 (DRUG), placebo for albuterol (DRUG).
Who is sponsoring clinical trial NCT01263197?
This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01263197 being conducted?
This trial has 1 study location across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.