Special Drug Use Investigation for VALTREX (Valaciclovir) (Suppression Prophylaxis)

NCT01390805 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 462

Last updated 2017-05-16

No results posted yet for this study

Summary

The purpose of this study is to collect and assess information on proper use of valaciclovir regarding safety and efficacy of long-term use in suppressive therapy for subjects with recurrent genital herpes.

Conditions

  • Genital Herpes

Interventions

DRUG

Valaciclovir Hydrochloride.

Sponsors & Collaborators

Principal Investigators

  • GSK Clinical Trials · GlaxoSmithKline

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-11-30
Primary Completion
2009-04-30
Completion
2011-03-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01390805 on ClinicalTrials.gov