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Spots Global Cancer Trial Database for A Study to Assess the Safety, Tolerability, Pharmacokinetics and Efficacy of Twice Daily Topical Applications of AP611074 5% Gel for up to 16 Weeks in Condyloma Patients

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Trial Identification

Brief Title: A Study to Assess the Safety, Tolerability, Pharmacokinetics and Efficacy of Twice Daily Topical Applications of AP611074 5% Gel for up to 16 Weeks in Condyloma Patients

Official Title: A Double-blind Placebo Controlled, Randomized, Phase II Study to Assess the Safety, Tolerability, Pharmacokinetics and Efficacy of Twice Daily Topical Applications of AP611074 5% Gel for up to 16 Weeks in Condyloma Patients

Study ID: NCT02724254

Conditions

Condyloma

Study Description

Brief Summary: This is a double-blind placebo controlled, randomized, phase 2 study to assess the safety, tolerability, pharmacokinetics and efficacy of twice daily topical applications of AP611074 5% Gel for up to 16 weeks in condyloma patients

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Anaconda Invesigational Site, Buenos Aires, , Argentina

Anaconda Investigational Site, Buenos Aires, , Argentina

Anaconda Investigational Site, Cordoba, , Argentina

Anaconda Investigational Site, Córdoba, , Argentina

Anaconda Investigational Site, Mendoza, , Argentina

Anaconda Investigational Site, Sante Fe, , Argentina

Anaconda Investigational Site, Concepción, , Chile

Anaconda Investigational Site, Santiago, , Chile

Anaconda Investigational Site, Cumbaya, , Ecuador

Anaconda Investigational Site, Guayaquil, , Ecuador

Anaconda Investigational Site, Quito, , Ecuador

Anaconda Investigational Site, Belgrade, , Serbia

Anaconda Investigational Site, Novi Sad, , Serbia

Contact Details

Name: Anna Novotney-Barry

Affiliation: Aviragen Therapeutics, Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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