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Multiple Dose Safety Study of SRX251 Capsules in Healthy Volunteers

2014-08-27 03:36:06 | BioPortfolio

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.

Study Design

Allocation: Randomized, Control: Placebo Control, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Conditions

Healthy

Intervention

SRX251

Location

Advanced Biomedical Research, Inc.
Hackensack
New Jersey
United States
07601

Status

Completed

Source

Azevan Pharmaceuticals

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:36:06-0400

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