Double-blind, Vehicle-controlled Study of the Efficacy and Safety of SADBE in Subjects With Recur… (NCT02965781) | Clinical Trial Compass
CompletedPhase 1/2
Double-blind, Vehicle-controlled Study of the Efficacy and Safety of SADBE in Subjects With Recurrent Herpes Labialis
United States139 participantsStarted 2016-12
Plain-language summary
This study evaluates the safety and efficacy of SADBE in the prevention of recurrent herpes labialis in adults. Two-thirds of the participants will receive a SADBE solution, while the other third will receive only the vehicle as a placebo control. The solutions will be administered topically to the patient's arms. The study will compare a single-arm application versus a two-arm application versus two placebo doses on the arm.
Who can participate
Age range18 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Age ≥18
* Clinical diagnosis of herpes labialis, which may be made at the screening visit based on the patient's self-reported history of symptoms. An active herpes labialis outbreak at the time of entry into the clinical trial will neither be required nor will be an exclusion criteria.
* Self report having four or more episodes of herpes labialis in the past 12 months
Exclusion Criteria:
* People that have had treatment with anti viral therapy within 2 weeks before sensitization dose.
* Pregnant or lactating females.
* Current or recurrent non-herpetic infection or any underlying condition that may predispose to infection or anyone who has been admitted to the hospital due to bacteremia, pneumonia or any other serious infection.
* Therapy with glucocorticoid or immunosuppressants at time of recruitment or within past 4 weeks, except for inhaled corticosteroids for asthma or topical steroids in sites other than face.
* History of malignancy (except patients with surgically cured basal cell or squamous cell skin cancers)
* History of organ transplantation
* HIV-positive status determined by history at screening or known history of any other immunosuppressive disease.
* Severe co-morbidities (diabetes mellitus requiring insulin, CHF (EF\<50% at baseline will be exclusionary) MI, CVA or TIA within 3 months of screening visit, unstable angina pectoris, oxygen-dependent severe pulmonary disease
* History of exposure to squaric acid or squaric acid dibutyl …
What they're measuring
1
Days to Next Herpes Labialis (Cold Sore) Episode From 43 Days After the First Dose up to 121 Days After the First Dose