Condition category
Urological and Genital Diseases
Date applied
Date assigned
Last edited
Retrospectively registered
Overall trial status
Recruitment status
No longer recruiting

Plain English Summary

Not provided at time of registration

Trial website

Contact information



Primary contact

Dr Roberto Gomez


Contact details

Sanabria 2353 1st floor
Buenos Aires

Additional identifiers

EudraCT number number

Protocol/serial number


Study information

Scientific title

Randomised, blind and placebo-controlled trial for the CIGB-300 perilesional application in two dose levels in the recurrent and non recurrent genital condyloma


Study hypothesis

Treatment is considered successful if the difference in the response in the reduction of the affected area is above 30% for any of the doses compared to placebo

Ethics approval

Independent Ethics Committee for Trials in Clinical Pharmacology (Comité Independiente de Etica para Ensayos en Farmacología Clínica) approved on the 13th of April 2009

Study design

Prospective randomised multicentre blinded study

Primary study design


Secondary study design

Randomised controlled trial

Trial setting

Not specified

Trial type


Patient information sheet

Not available in web format, please use contact details to request a patient information sheet


Recurrent and non-recurrent genital condyloma


Patients will be randomised to 1 of 3 treatment arms
1. Placebo
2. CIGB-300 - 5 mg
3. CIGB-300 - 15 mg

A two week screening visit will take place to assess patient eligibility, at least 2 to 5 target lesions (area of the lesion between 20 to 80 mm2), should be identified. Patients included in the study will be randomly assigned to one of three study arms. Treatment consists of 3 perilesional applications at the base of the target lesion every 48 hours with a window of ±24hs.
After each application the potential local and systemic adverse events will be identified and monitored.
After the last application is made, weekly clinical evaluations for 3 weeks and then every two weeks, until week 12 will take place. At this time, clinical assessment of efficacy will be carried out that will define the response to treatment.
After this visit, patients will be followed every 3 months until one year after the last treatment has been completed to confirm response and long-term security of the CIGB-300 application.
At screening, at 2 and 8 weeks as well as at 6 and 12 months post-treatment blood studies will be conducted to assess the safety from the systemic point of view.

Intervention type



Phase III

Drug names

Primary outcome measures

1. Assess the safety of the perilesional application of CIGB-300 for the treatment of recurrent and non-recurrent condylomatous lesions
2. To assess CIGB-300 effect in the resolution of recurrent and non-recurrent, when considering the reduction in the number of lesions, lesion total area and the occurrence of recurrence of episodes

Secondary outcome measures

1. To assess the effect of CIGB-300 perilesional application in the reduction in number and area of genital warts lesions treated directly
2. To determine the locoregional effect of the product under study by assessing the area and number of genital warts not directly treated
3. To evaluate the possible effect of the product to avoid recurrence of the lesions resolved during treatment, assessed post-treatment
4. Define the optimal dose, in comparison with placebo
5. Identify, assess and report adverse events that occur during treatment in each treatment group so to identify the safest and most effective dose

Overall trial start date


Overall trial end date


Reason abandoned


Participant inclusion criteria

1. Informed consent signed by the patient
2. Women with clinical diagnosis of recurrent and non recurrent genital condyloma
3. Presence of a condylomatous lesion or area of external confluent condylomatous lesions of not less than 20 or more than 80 mm2
4. The number of warts should be between 2 and 20
5. External genital warts or in perigenital regions
6. Negative pregnancy test
7. Age between 21 and 65 years inclusive

Participant type


Age group

Not Specified


Not Specified

Target number of participants


Participant exclusion criteria

1. Having received surgery treatment, ablative or immunomodulator treatment during the 30 days prior to inclusion
2. Presence of genital warts only located in the cervix, vagina, bladder or rectum
3. Pregnancy and lactation
4. Patients of childbearing age who are not using an adequate contraception method during treatment to prevent pregnancy. 5. Inadequately controlled chronic diseases (hypertension, diabetes, chronic kidney failure, heart failure, hyperthyroidism, malignant neoplasms, epilepsy, severe mental depression)
6. Patients with previous diagnosis of bleeding disorders and other chronic blood disorders (von Willebrand disease, haemophilia, leukaemia) or use of anticoagulants within 30 days before the study
7. Current genital herpes, which requires application of topical antivirals
8. Immunosuppressive disease, current intake of immunosuppressive/ immunomodulatory drugs within 30 days before the study.
9. Autoimmune Diseases (Lupus Erythematosus, Rheumatoid Arthritis, Multiple Sclerosis, Diabetes)
10. Severe allergy history as urticaria, dermatitis or persistent bronchitis and bronchial asthma
11. Febrile illness (temperature greater than 38ºC) at the time or within 24 hours prior to administration of the product or suspected acute infectious disease by clinical examination
12. Diseases that compromise the patient's consciousness or the ability to give informed consent or to collaborate in the study
13. Concomitant skin lesions that prevent the administration of condylomatous lesions at the proposed site
14. Participating in another clinical trial

Recruitment start date


Recruitment end date



Countries of recruitment

Argentina, Uruguay

Trial participating centre

Sanabria 2353 1st floor
Buenos Aires

Sponsor information


Laboratorio Elea SACIFyA (Argentina)

Sponsor details

Sanabria 2353 1st floor
Buenos Aires

Sponsor type




Funder type


Funder name

Laboratorio Elea SACIFyA (Argentina)

Alternative name(s)

Funding Body Type

Funding Body Subtype


Results and Publications

Publication and dissemination plan

Not provided at time of registration

Intention to publish date

Participant level data

Not provided at time of registration

Results - basic reporting

Publication summary

Publication citations

Additional files

Editorial Notes