Open Label Safety Study of Xerese Cream in the Treatment of Recurrent Herpes Labialis in Children 6-11 Years Old
Status: | Completed |
---|---|
Conditions: | Infectious Disease, Women's Studies |
Therapuetic Areas: | Immunology / Infectious Diseases, Reproductive |
Healthy: | No |
Age Range: | Any |
Updated: | 2/4/2013 |
Start Date: | March 2012 |
End Date: | May 2013 |
Contact: | Karen Watson, BS |
Email: | kwatson@tklresearch.com |
Phone: | 2015870505 |
An Open Label Multi Center Phase III Subject/Caregiver Initiated Safety Study of Xerese(Acyclovir and Hydrocortisone)Cream 5%/1% in the Treatment of Recurrent Herpes Labialis in Children
To test the safety of Xerese (acyclovir and hydrocortisone)Cream 5%/1% for the treatment of
recurrent cold sores in children ages 6-11yrs after 5 days of treatment.
Inclusion Criteria:
- Male or female, age 6-11 years at time of enrollment
- General good health, as judged by the Investigator
- History of recurrent herpes labialis with at least two (2) recurrences during the
last twelve (12) months, as based on interview with the subject or subject's
caregiver
- Agreement to refrain from using other topical medical, over-the counter (OTC), or
cosmetic products in or around the oral area during the herpes recurrence
- Agreement to refrain from mechanical disruption of the area affected by herpes
labialis during the study recurrence
- Subjects and their legally acceptable representative(s) must voluntarily sign and
date the informed assent (subject) and consent (legally authorized representative).
- Willingness to comply with all requirements of the study.
Exclusion Criteria:
- Any evidence of an immunosuppressed state of the subject due to underlying disease
(e.g. HIV infection) or concomitant treatment (e.g. cancer chemotherapy)
- Significant skin conditions that occur in the area typically affected by herpes
recurrences, and that would interfere with assessment of lesions such as atopic
dermatitis, acne, eczema, psoriasis or chronic vesiculobullous disorders
- Administration of an investigational drug or within 30 days prior to inclusion, or
concurrent participation in another research study
- Administration of an immunomodulatory agent within the past 30 days
- History of immediate hypersensitivity or serum sickness reaction to any nucleoside
analog antiviral agent, or to any topical steroid, or to the vehicle
- Clinically relevant abnormal physical findings at screening which, in the opinion of
the investigator, would interfere with the objectives of the study or that may
preclude compliance with the study procedures Nursing or pregnant (Pubescent females
require pregnancy testing)
We found this trial at
10
sites
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