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Clinical Trial Summary

Study aimed to evaluate the efficacy and tolerance of Lazolex®, an emollient gel, to treat mucocutaneous lesions caused by herpes simplex virus.


Clinical Trial Description

A single-center, single-arm, open-label, phase II clinical trial was conducted with 30 patients divided into two groups: 15 patients with herpes simplex virus type 1 (HSV-1) infections and 15 with herpes simplex virus type 2 (HSV-2) infections. All received topical treatment with Lazolex® Gel four times daily for 10 days. The efficacy and tolerance of the treatment were evaluated on day 10 and day 20 after the study started. In addition, recurrence rates were evaluated before treatment with Lazolex® and after a 4-year follow-up period after treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06089252
Study type Interventional
Source Iveriapharma LLC
Contact
Status Completed
Phase Phase 2
Start date November 27, 2007
Completion date January 28, 2008

See also
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