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NCT00990301 · ClinicalTrials.gov registry record · Phase 1
A Study to Compare the Relative Bioavailability of Moexipril HCl/Hydrochlorothiazide in Healthy Adult Volunteers Under Fasting Conditions
A Phase 1 study of Healthy, sponsored by Paddock Laboratories.
- Completed
- Registry status
- Phase 1
- Development phase
- 48
- Enrollment target
- 1
- Study location
NCT00990301: Completed Phase 1 study of Healthy, sponsored by Paddock Laboratories.
NCT00990301 is a Phase 1 study of Healthy that has completed, run by Paddock Laboratories. The registered enrollment target is 48 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00990301, a Phase 1 study of Healthy, has completed, sponsored by Paddock Laboratories.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 48 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study was to evaluate the relative bioavailability of Paddock Laboratories, Inc.'s test formulation of Moexipril/ Hydrochlorothiazide 15mg/25mg tablets with a reference formulation Uniretic®(Moexipril/ Hydrochlorothiazide) 15mg/25mg tablets, under fasting conditions.
Conditions Studied
Interventions
- DRUG Moexipril HCl/ Hydrochlorothiazide 15mg/ 25mg Tablet, Paddock Laboratories, Inc.
- DRUG Uniretic® 15mg/25mg Tablets
Study Locations (1)
Pennsylvania
- Novum Pharmaceutical Research Services - Pittsburgh
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 48 participants |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00990301
The ClinicalTrials.gov registry entry for NCT00990301 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 647-participant average among 1,090 other Healthy trials with a reported enrollment target (93% lower). The listed sponsor is Paddock Laboratories, which has 2 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Healthy appearing as the primary indexed condition, and to 2 interventions - of which Moexipril HCl/ Hydrochlorothiazide 15mg/ 25mg Tablet, Paddock Laboratories, Inc. is the first listed.
NCT00990301 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT00990301 about?
NCT00990301 is a clinical study titled "A Study to Compare the Relative Bioavailability of Moexipril HCl/Hydrochlorothiazide in Healthy Adult Volunteers Under Fasting Conditions". The purpose of this study was to evaluate the relative bioavailability of Paddock Laboratories, Inc.'s test formulation of Moexipril/ Hydrochlorothiazide 15mg/25mg tablets with a reference formulation Uniretic®(Moexipril/ Hydrochlorothiazide) 15mg/25mg tablets, under fasting conditions.
What is the current status of trial NCT00990301?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 48 participants.
What conditions does trial NCT00990301 study?
This clinical trial studies the following conditions: Healthy.
What interventions are being tested in trial NCT00990301?
The interventions under investigation include: Moexipril HCl/ Hydrochlorothiazide 15mg/ 25mg Tablet, Paddock Laboratories, Inc. (DRUG), Uniretic® 15mg/25mg Tablets (DRUG).
Who is sponsoring clinical trial NCT00990301?
This trial is sponsored by Paddock Laboratories, which has 2 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00990301 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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