Efficacy of Acyclovir in Combination With a Glucocorticosteroid on UV-Induced Herpes Labialis

Herpes Labialis Clinical Trial

Official title:

Efficacy of Acyclovir in Combination With a Glucocorticosteroid on UV-Induced Herpes Labialis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00736437
• Other study ID #: 98-609-013
• Status: Completed
• Phase: Phase 2
• First received: August 14, 2008
• Last updated: August 14, 2008
• Start date: August 1999
• Est. completion date: August 2000

Study information

• Verified date: August 2008
• Source: Medivir
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The primary objective was to compare the efficacy of ME-609 cream vs placebo cream on the time to healing (loss of hard crust) of delayed classical herpes labialis (HSV) lesions experimentally induced after ultra violet radiation (UVR) exposure.

Description:

The primary objective was to compare the efficacy of ME-609 cream vs placebo cream on the time to healing (loss of hard crust) of delayed classical herpes labialis (HSV) lesions experimentally induced after ultra violet radiation (UVR) exposure. Secondary objectives were to compare the time to normal skin, incidence of lesion development (number and type of lesions), maximum lesion size, length of lesion stages, frequency/severity/duration of pain, frequency/severity/duration of tenderness, redness and/or oedema in the UVR exposed area, frequency of virus positive lesions, time to cessation of viral shedding and safety of ME-609 cream vs placebo cream.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 417
• Est. completion date: August 2000
• Est. primary completion date: August 2000
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Aged 18 years or older

• A history of reactivation of recurrent herpes labialis with overexposure to sunlight in the last 12 months, or 2 or more cold sore lesions in the last 12 months

• Generally healthy as determined by medical history and verbal interview

• Females who were still able to conceive were to have had a negative pregnancy test on enrolment

• Fritzpatrick skin type category of I to IV

Exclusion Criteria:

• Previous inclusion in this study

• Participation in clinical investigational drug studies in the 4-week period prior to enrolment

• Participation in any herpes UVR reactivation study within the previous 3 months

• Previous herpes vaccination at any time

• Occurrence of herpes labialis (end of episode) within one month prior to enrolment

• Inflammatory, congenital or iatrogenic underlying immunodeficiency disorders

• Use of topical steroids in or near the face or on the forearms, systemic steroids (within 30 days from enrolment) or anti-inflammatory drugs (within 10 days from enrolment)

• Women who were pregnant, lactating or breast feeding

• Women of child bearing potential not using adequate contraception as judged by the investigator

• Recent history of alcohol or drug abuse which in the opinion of the investigator could interfere with compliance

• Significant skin disease such as atopic dermatitis or eczema, that would interfere with the assessment of lesions

• Allergy or hypersensitivity to steroids, acyclovir, penciclovir and/or other nucleoside analogues

• Administration of any drug commonly associated with photosensitivity (tetracycline, Retin A) within one week of UVR exposure

• Any antiviral therapy within 14 days prior to enrolment

• History of allergy or sensitivity to sunscreen

• History of herpes keratitis

Study Design

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

Related Conditions & MeSH terms

• Herpes Labialis

Intervention

Drug:
• ME-609
Cream applied topically 6 times daily over the UVR exposed area
• Vehicle
Treatment applied 6 times daily over the UVR exposed area

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Medivir

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	time to healing (loss of hard crust) of delayed classical herpes labialis (HSV) lesions experimentally induced after ultra violet radiation (UVR) exposure.		5 days	No
Secondary	time to normal skin, incidence of lesion development, max lesion size, length of lesion stages, pain and tenderness, redness and/or oedema in the UVR exposed area, frequency of virus positive lesions, time to cessation of viral shedding and safety		5 days	No