Trial intelligence / Profile preview

Oral Naloxone for Opioid-Induced Constipation

NCT00020605Phase 3Unknown

Sponsor
Dana-Farber Cancer Institute
Start
May 2000
Modality
Orthosteric Ligands
Countries
1
01

Overview

Phase 3, randomised, double-blind trial in opioid-induced constipation (OIC) comparing Naloxone with Placebo (2 arms). Primary endpoint: Long-term safety and efficacy of oral naloxone at 72 weeks. Status: unknown.

02

Drugs

naloxone
03

Conditions

opioid-induced constipation (OIC)

Beyond the preview

Go deeper on NCT00020605.

Study design, results and competitive context are available in the Gosset platform where reported.

Study design & results

Available in the Gosset platform where reported.

Competitive context

Available in the Gosset platform where reported.

Bring the full picture into focus.

See how Gosset can support your research on NCT00020605.

Gosset Free

Get started with Gosset.

Enter your corporate email.

Work email preferred.

Book a call