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NCT00532467 · ClinicalTrials.gov registry record · Phase 1

Multiple Dose Safety Study of SRX251 Capsules in Healthy Volunteers

A Phase 1 study of Healthy, sponsored by Azevan Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
50
Enrollment target
1
Study location

NCT00532467: Completed Phase 1 study of Healthy, sponsored by Azevan Pharmaceuticals.

NCT00532467 is a Phase 1 study of Healthy that has completed, run by Azevan Pharmaceuticals. The registered enrollment target is 50 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00532467, a Phase 1 study of Healthy, has completed, sponsored by Azevan Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
50 participants
Enrollment target
1
Study location

Study Summary

This study is the second study to evaluate SRX251 in healthy volunteers and it represents the first multiple dose study. The primary objective of this study is to evaluate the safety and tolerability of escalating multiple oral doses of SRX251 capsules for 5 days in healthy adult volunteers. Levels of the drug in blood plasma will also be determined.

Conditions Studied

Interventions

  • DRUG SRX251

Study Locations (1)

New Jersey

  • Advanced Biomedical Research, Inc. - Hackensack

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2007-09
Est. Completion 2008-02
Phase Phase 1

Sponsor

Azevan Pharmaceuticals

8 total trials

What the Registry Record Tells You About NCT00532467

The ClinicalTrials.gov registry entry for NCT00532467 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 50 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 (92% lower). The listed sponsor is Azevan Pharmaceuticals, which has 8 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Healthy appearing as the primary indexed condition, and to 1 intervention - of which SRX251 is the first listed.

NCT00532467 reports 1 study location spanning 1 distinct geographic area - top geographies include New Jersey.

Frequently Asked Questions

What is clinical trial NCT00532467 about?

NCT00532467 is a clinical study titled "Multiple Dose Safety Study of SRX251 Capsules in Healthy Volunteers". This study is the second study to evaluate SRX251 in healthy volunteers and it represents the first multiple dose study. The primary objective of this study is to evaluate the safety and tolerability of escalating multiple oral doses of SRX251 capsules for 5 days in healthy adult volunteers. Levels ...

What is the current status of trial NCT00532467?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 50 participants. The study started on 2007-09. Estimated completion is 2008-02.

What conditions does trial NCT00532467 study?

This clinical trial studies the following conditions: Healthy.

What interventions are being tested in trial NCT00532467?

The interventions under investigation include: SRX251 (DRUG).

Who is sponsoring clinical trial NCT00532467?

This trial is sponsored by Azevan Pharmaceuticals, which has 8 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00532467 being conducted?

This trial has 1 study location across New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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, the data changelog, or report a data error.