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Extension Study to Evaluate the Safety of Q8003 in Patients With Acute Moderate to Severe Pain

2014-07-24 14:19:44 | BioPortfolio

Summary

This is a Phase 3 double-blind, multiple dose safety extension study of Q8003 administered at daily doses up to 36 mg morphine/24 mg oxycodone (Q8003 36mg/24mg) over a treatment period of up to 4 weeks. Patients with acute moderate to severe pain who have completed participation in one of the designated QRxPharma, Inc. acute pain lead-in studies will be eligible for this trial.

Description

The currently designated acute pain lead-in study is Study Q8003-007, which is a safety and efficacy study of Q8003 in the management of post-bunionectomy pain.

Study Design

Allocation: Randomized, Control: Placebo Control, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Conditions

Acute Moderate to Severe Pain

Intervention

Q8003, Placebo

Location

Advanced Clinical Research Institute
Anaheim
California
United States
92801

Status

Completed

Source

QRxPharma Inc.

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-07-24T14:19:44-0400

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