Status:
COMPLETED
CyPep-1 in Cutaneous Warts
Lead Sponsor:
Centre for Human Drug Research, Netherlands
Conditions:
Cutaneous Warts
Eligibility:
All Genders
18-65 years
Phase:
PHASE1
Brief Summary
This Phase 1 study is intended to explore the safety, tolerability, pharmacodynamics and efficacy of topical CyPep-1 as a potential treatment for HPV-associated conditions. Since this is a first-on-hu...
Detailed Description
This study has a phase 1, randomized, vehicle-controlled, double-blind, single center design to explore the safety, tolerability and pharmacodynamics (PD) of topically applied CyPep-1 in otherwise hea...
Eligibility Criteria
Inclusion
- Healthy subjects (male, non-pregnant female), 18 to 65 years of age, inclusive. (Healthy status is defined by absence of evidence of any clinical significant/uncontrolled active or chronic disease following a detailed medical and surgical history, a complete physical examination including vital signs,12-lead ECG, haematology, blood chemistry, and urinalysis);
- Body mass index (BMI) between 18 and 35 kg/m2, inclusive;
- Free of clinically significant systemic or dermatologic disorders, which, in the opinion of the investigator, will interfere with the study results or increase the risk of Adverse Events;
- Have at least 1 (non-peri/subungual) common wart on the, preferably, dorsal/palmar side of the hand / fingers which is 3-10 mm (inclusive) in diameter in its longest dimension on the plane of the skin;
- If female of childbearing potential, have a negative urine pregnancy test at Screening/Day 0, and are willing to use effective contraception during the study (i.e. oral, implanted, injectable, IUD, diaphragm, condom, tubal ligation, abstinence, or are in a monogamous relationship with a partner who has had a vasectomy);
- Able to participate and willing to give written informed consent and to comply with the study restrictions;
- Ability to communicate well with the investigator in the Dutch language;
- Willing to refrain from using cosmetics or other topical products in the treatment area for the duration of the study;
- Agree not to use wart-removing products (prescription or over-the-counter) in the target area or prohibited medications other than the study medication during the course of the study.
Exclusion
- Any clinically significant abnormality as determined by medical history taking and physical examinations obtained during the screening visit that in the opinion of the investigator would interfere with the study objectives or compromise subject safety;
- Not willing to use effective (double barrier) contraception until at least 3 months after last study drug application;
- For women: a positive pregnancy test and/or breastfeeding at screening or women who plan to become pregnant;
- A positive test for drugs of abuse at screening;
- History of alcohol or illicit drug abuse (alcohol abuse defined as alcohol consumption \> 21 units/week);
- Positive test results for Hepatitis B, Hepatitis C or HIV;
- Have used salicylic acid or any other over-the-counter wart-removing product including cryotherapy in the treatment area within 28 days prior to first study drug application;
- Have required systemic intake of immunosuppressive or immunomodulatory medication (including oral or parenteral corticosteroids) within 60 days prior to first study drug application or during the course of the study. Routine use of inhaled or intranasal corticosteroids during the study is allowed;
- Have any current and / or recurrent clinical significant skin infection in the treatment area other than common warts;
- Have a known sensitivity to any of the investigational product ingredients;
- Participation in an investigational drug or device study within 3 months prior to screening or more than 4 times in the past year;
- Donation of blood or blood loss of \>500 mL within 3 months prior to screening or donation of plasma within 14 days
- Not having a general practitioner;
- Not willing to give permission to have the general practitioner to be notified upon participation in this study;
- Any condition that in the opinion of the investigator would complicate or compromise the study or the well-being of the subject.
- Part 2 only:
- \- Have treatment resistant / persistent warts as defined as one of the following:
- More than 5 different failed treatments including topical formulations and cryotherapy
- Longer than 6 years presence of the target wart
- Having received active treatment in a clinical trial with an experimental drug for cutaneous warts.
Key Trial Info
Start Date :
March 11 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 20 2019
Estimated Enrollment :
56 Patients enrolled
Trial Details
Trial ID
NCT03846648
Start Date
March 11 2019
End Date
December 20 2019
Last Update
August 3 2021
Active Locations (1)
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1
Centre for Human Drug Research
Leiden, South Holland, Netherlands, 2333 CL