Safety and Efficacy Study to Test Topical AS101 for External Genital Warts

NCT ID: NCT01555112

Last Updated: 2013-08-15

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 12 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-03-31
• Study Completion Date: 2013-07-31

Brief Summary

The purpose of this study is to determine whether the improved topical ointment formulation, AS101, is safe and effective in the treatment of external genital warts in females.

Detailed Description

Human papillomavirus (HPV)-induced condyloma acuminata (CA), commonly known as anogenital or genital warts, is among the most common sexually transmitted diseases. There are a wide variety of available treatments of genital warts, but none are considered completely effective. It has been suggested that AS101 works by stimulating the innate and acquired arms of the immune system.

In previous proof-of-concept clinical study AS101 topical cream was tested on HPV warts and shown cure in high percentages. However the cream formulation was unstable therefore a new formulation was developed mainly for the carrier. In this study the improved AS101 ointment will be tested in female patients with external genital warts in an open study to assess its safety and efficacy.

Conditions

Wart; External Genital Organs; Condyloma Acuminata

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Topical AS101

15% AS101 ointment applied twice a day for treatment of external genital warts.

Group Type: EXPERIMENTAL

Topical AS101

Intervention Type: DRUG

AS101 15% ointment will be applied topically twice daily on external genital warts for up to 16 weeks.

Interventions

Topical AS101

AS101 15% ointment will be applied topically twice daily on external genital warts for up to 16 weeks.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Women 18 years of age and in good health;
• Must sign an ethics committee approved informed consent form and be able to adhere to study visits and protocol requirements;
• Women must agree to avoid sexual contact while the ointment is on their skin;
• All study participants who are sexually active must use a barrier protection method of contraception such as condom in addition to another birth control measure such as oral contraceptives, intrauterine device, spermicide or surgical sterilization during treatment and for 60 days after completion of treatment;
• Patients with first clinical diagnosis of external genital warts, in the external genitalia including vulva (labia minora and majora), inguinal folds, pubic area, perineum, perianal, or buttocks areas;
• A minimum of one lesion and a maximum of 10 lesions identified at study entry, and the maximum diameter of the largest wart is no larger than 10 mm;
• Papanicolaou smears must be obtained in all females within 12 months of Day 1 and be negative for evidence of high grade intraepithelial neoplasia. Women with high grade intraepithelial neoplasia on cytology will be eligible if subsequent colposcopy with biopsy of suspicious area is negative for high grade squamous intraepithelial lesions (Grade 2 or 3). Atypia, HPV effect, and low grade intraepithelial lesions (Grade 1) are acceptable.

Exclusion Criteria

• Participation in an investigational trial within 30 days prior to Day 1;
• Use of systemic steroids within 30 days of Day 1;
• Previous participation in a trial investigating AS101 for any indication.
• Any prior treatment for genital warts prior to participation;
• Topical and systemic immunosuppressive or immunomodulatory medications (including corticosteroids) within 30 days prior Day 1, and while on study;
• Known history of HIV, HBV and HCV viral infection.
• Current active infection with herpes genitalis or history of herpes genitalis infection within the last 30 days prior to Day 1 (patients on long-term suppressive antiviral therapy are eligible);
• Current and/or recurrent pathologically relevant genital infections other than genital warts;
• Diagnosis of high-grade cervical dysplasia;
• Internal anogenital, vaginal, urethral and cervical warts requiring treatment;
• Chronic or acute skin condition that might interfere with the evaluation of the treatment or study drug effect;
• Cutaneous surgery, including cryosurgery, to genital area within 30 days of Day 1;
• Screening laboratory tests results from a complete blood count (CBC), chemistry panel, urine pregnancy test and urinalysis obtained during screening (Day -14 to Day 0):

• Must be within the site laboratory's defined normal reference ranges, and/or according to the Investigator's decision;
• Urine pregnancy test in females of childbearing potential must be negative;
• Inadequate renal function: Serum Creatinine > 2.0mg/dL (> 2.0 ULN);
• Inadequate liver function: Serum (total) Bilirubin > 2 mg/dl or ALT and/or AST greater than two times the upper limit of the reference range.
• Uncontrolled infection or acute severe febrile illness;
• Diagnosed as having uncontrolled autoimmune disease;
• Pregnant or lactating;
• Current drug or alcohol abuse that may interfere with the objectives of the study;
• Known allergy to AS101 or any component of the investigational formulation;
• Subjects with any other clinically significant medical condition, psychiatric condition or laboratory abnormality which would, in the judgment of the Investigator, interfere with the subject's ability to participate in the trial.

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

BioMAS Ltd

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Shabtai Romano, MD

Role: PRINCIPAL_INVESTIGATOR

Ha'Emek Medical Center, Afula, Israel

Locations

Gynecology department, Haemek MC

Afula, , Israel

Countries

Israel

Other Identifiers

AS101-IL#001

Identifier Type: -

Identifier Source: org_study_id