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Clinical Trial Summary

The study is designed to assess the efficacy and safety of patient-initiated therapy with famciclovir 1500 mg o.d. or 750 mg b.i.d. for one day treatment in adult men and women with recurrent herpes labialis


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00248144
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 4
Start date October 2003
Completion date July 2007

See also
  Status Clinical Trial Phase
Not yet recruiting NCT03977792 - An Open Label Study to Evaluate the Safety and Efficacy of BOR15001L7 for the Treatment of Cold Sores in Patients With Recurrent Herpes Labialis Phase 2
Active, not recruiting NCT05098938 - A Study to Compare Sitavig (Acyclovir) Buccal Tablet With a Placebo in the Treatment of Herpes Labialis in Participants Whose Immune System Works Normally Phase 3
Completed NCT01985321 - Safety and Efficacy of Merlin (Ethanol and Glycolic Acid Mixture) for the Treatment of Cold Sores Phase 2
Completed NCT03192306 - Safety and Efficacy of Merlin (Ethanol and Glycolic Acid Mixture) for Episodic Treatment of Cold Sores Phase 2
Completed NCT01324466 - A Multicenter Study of NB-001 in the Treatment of Recurrent Herpes Labialis (SHaRCS) Phase 3
Completed NCT00914745 - Place Controlled Study to Treat Recurrent Herpes Labialis. Phase 2