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NCT00492323

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group With a Crossover Confirmation Period Study of RWJ-333369 for the Treatment of Postherpetic Neuralgia.

Completed Phase 2 Last updated 27 April 2018
What this trial tests

Phase 2 trial testing placebo in Postherpetic Neuralgia in 91 participants. Completed in 1 June 2008.

Timeline
1 March 2007
Primary endpoint
1 June 2008
1 June 2008

Quick facts

Lead sponsorSK Life Science, Inc.
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingquadruple
Primary purposetreatment
Enrollment91
Start date1 March 2007
Primary completion1 June 2008
Estimated completion1 June 2008

Drugs / interventions tested

Conditions studied

Sponsor

SK Life Science, Inc. — full company profile →

Who can join

Adults 18 to 85, any sex, with Postherpetic Neuralgia or Neuralgia. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The purpose of this study is to evaluate the safety, effectiveness, and tolerability of 200 mg of RWJ-333369 given twice daily compared with placebo in the treatment of postherpetic neuralgia.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Postherpetic Neuralgia

Currently open trials in the same condition.

Other SK Life Science, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00492323.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing