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NCT00940121 · ClinicalTrials.gov registry record · Phase 1
Pharmacokinetics of Oral Mirabegron With Different Release Rates Versus Intravenous (IV) Mirabegron
A Phase 1 study of Healthy and Pharmacokinetics of Mirabegron, sponsored by Astellas Pharma.
- Completed
- Registry status
- Phase 1
- Development phase
- 91
- Enrollment target
- 1
- Study location
NCT00940121 is a Phase 1 study of Healthy and Pharmacokinetics of Mirabegron that has completed, run by Astellas Pharma. The registered enrollment target is 91 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (86% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00940121, a Phase 1 study of Healthy and Pharmacokinetics of Mirabegron, has completed, sponsored by Astellas Pharma.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 91 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to assess the pharmacokinetics of three doses of oral mirabegron formulations with three different release rates versus three doses of mirabegron administered intravenously; to study safety and side effects of the oral and IV doses of mirabegron.
Conditions Studied
Interventions
- DRUG mirabegron
Study Locations (1)
Washington
- - Tacoma
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 91 participants |
| Start Date | 2009-04-30 |
| Est. Completion | 2009-07-13 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00940121
The ClinicalTrials.gov registry entry for NCT00940121 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 91 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (86% lower). The listed sponsor is Astellas Pharma, which has 165 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Healthy appearing as the primary indexed condition, and to 1 intervention - of which mirabegron is the first listed.
NCT00940121 reports 1 study location spanning 1 distinct geographic area - top geographies include Washington.
Frequently Asked Questions
What is clinical trial NCT00940121 about?
NCT00940121 is a clinical study titled "Pharmacokinetics of Oral Mirabegron With Different Release Rates Versus Intravenous (IV) Mirabegron". The purpose of this study is to assess the pharmacokinetics of three doses of oral mirabegron formulations with three different release rates versus three doses of mirabegron administered intravenously; to study safety and side effects of the oral and IV doses of mirabegron.
What is the current status of trial NCT00940121?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 91 participants. The study started on 2009-04-30. Estimated completion is 2009-07-13.
What conditions does trial NCT00940121 study?
This clinical trial studies the following conditions: Healthy, Pharmacokinetics of Mirabegron.
What interventions are being tested in trial NCT00940121?
The interventions under investigation include: mirabegron (DRUG).
Who is sponsoring clinical trial NCT00940121?
This trial is sponsored by Astellas Pharma, which has 165 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00940121 being conducted?
This trial has 1 study location across Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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