Tolerability and Pharmacokinetic Study of Econazole Nitrate Plus Benzydamine HCl Vaginal Pessary

Sponsor

Aziende Chimiche Riunite Angelini Francesco S.p.A (Industry)

Overall Status

Completed

CT.gov ID

NCT02720783

Collaborator

Cross Research S.A. (Industry)

Enrollment

Location

Arms

7.3

Actual Duration (Months)

6.7

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The primary objective of the study is to evaluate the local tolerability of the new Econazole/Benzydamine pessary, in comparison with Econazole and Benzydamine stand-alone products and placebo. Pharmacokinetics of the study products after single and multiple applications o.d. for 3 days, overall local and general tolerability, safety and comfort of use will also be evaluated.

Condition or Disease	Intervention/Treatment	Phase
Healthy Women	Drug: Econazole nitrate 150 mg plus Benzydamine HCl 6 mg vaginal pessary Drug: Placebo plus Econazole nitrate 150 mg vaginal pessary Drug: Placebo plus Benzydamine HCl 6 mg vaginal pessary Drug: Placebo vaginal pessary	Phase 1

Study Design

Study Type:

Interventional

Actual Enrollment :

49 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

Triple (Participant, Investigator, Outcomes Assessor)

Primary Purpose:

Other

Official Title:

A Phase I Study of a Novel Antimycotic Vaginal Pessary Formulation (Econazole Nitrate 150 mg + Benzydamine HCl 6 mg) Administered Once Daily for 3 Days to Healthy Women

Actual Study Start Date :

Mar 4, 2016

Actual Primary Completion Date :

Oct 12, 2016

Actual Study Completion Date :

Oct 12, 2016

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Econazole nitrate 150 mg plus Benzydamine HCl 6 mg One vaginal pessary (2.7 g) of Econazole nitrate 150 mg plus Benzydamine HCl 6 mg, once daily, for 3 consecutive days	Drug: Econazole nitrate 150 mg plus Benzydamine HCl 6 mg vaginal pessary Econazole nitrate 150 mg plus Benzydamine HCl 6 mg vaginal pessary
Active Comparator: Placebo plus Econazole nitrate 150 mg One vaginal pessary (2,7 g) of Placebo plus Econazole nitrate 150 mg, once daily, for 3 consecutive days	Drug: Placebo plus Econazole nitrate 150 mg vaginal pessary
Active Comparator: Placebo plus Benzydamine HCl 6 mg One vaginal pessary (2,7 g) of Placebo plus Benzydamine HCl 6 mg, once daily, for 3 consecutive days	Drug: Placebo plus Benzydamine HCl 6 mg vaginal pessary
Placebo Comparator: Placebo One vaginal pessary (2.7 g) of Placebo, once daily, for 3 consecutive days	Drug: Placebo vaginal pessary

Outcome Measures

Primary Outcome Measures

Local Adverse Drug Reactions (ADRs) [Up to 7 days after administration]
Occurence of local ADRs reported by the subjects as 1-3 scores for pruritus, burning sensation, pain, stinging and dryness; occurrence of all the other local Adverse Events (AEs) referred by the subjects; occurrence of all the local ADRs revealed by the Investigator/ Gynaecologist

Secondary Outcome Measures

Econazole (free base), benzydamine (free base) and benzydamine N-oxide (free base) plasma concentrations [At pre-dose (0), 1, 2, 3, 4, 6, 8, 12, 24 hours after the first (day 1) and the last dose (day 3)]
Area under the plasma concentration versus time curve [AUC(0-t)] of econazole (free base), benzydamine (free base) and benzydamine N-oxide (free base) [At pre-dose (0), 1, 2, 3, 4, 6, 8, 12, 24 hours after the first (day 1) and the last dose (day 3)]
Overall local tolerability assessment scale [At final visit (from day 5 to day 8)]
Occurrence of all AEs and ADRs [5-8 days]
Change from screening in laboratory parameters [From screening (from day -21 to day -7) at final visit (from day 5 to day 8)]
Questionnaire for the comfort of use [At final visit (from day 5 to day 8)]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 55 Years

Sexes Eligible for Study:

Female

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Informed consent: signed written informed consent before inclusion in the study.
Sex and age: healthy women, aged 18-55 years old inclusive.
Body Mass Index (BMI): 18.5-30 kg/m2 inclusive.
Vital signs: systolic blood pressure 100-139 mmHg, diastolic blood pressure 50-89 mmHg, heart rate 50-90 bpm, measured after 5 min at rest (sitting position).
Full comprehension: ability to comprehend the full nature and purpose of the study, including possible risks and side effects; ability to co-operate with the Investigator and to comply with the requirements of the entire study.
Sexual abstinence: agreement to sexual abstinence during the study.
Contraception and fertility: women of child-bearing potential, even if sexually abstinent during the study as required by the study inclusion criteria, must be using at least one reliable method of contraception, as follows:
hormonal oral, implantable, transdermal, or injectable contraceptives for at least 2 months before the screening visit;
a non-hormonal intrauterine device [IUD] for at least 2 months before the screening visit;
a male sexual partner who agrees to use a male condom;
a vasectomised sexual partner. Female participants of non-child-bearing potential will be admitted. For all female subjects, pregnancy test result must be negative at screening and on day 1.
PAP test: negative PAP test result (i.e. normal PAP test result without atypical cells) at screening.

Exclusion Criteria:

ECG (12-leads, supine position): clinically significant abnormalities.
Physical findings: clinically significant abnormal physical findings which could interfere with the objectives of the study as judged by the Investigator.
Laboratory analyses: clinically significant abnormal laboratory values indicative of physical illness.
Allergies: ascertained or presumptive hypersensitivity (including allergies) to the active ingredients (econazole nitrate and/or benzydamine HCl) and/or formulations' excipients or related drugs, e.g. other azoles; history of anaphylaxis to drugs or allergic reactions in general, which the Investigator considers may affect the outcome of the study.
Diseases: relevant history of renal, hepatic, gastrointestinal, genitourinary, cardiovascular, respiratory, skin, haematological, endocrine or neurological diseases that may interfere with the aim of the study or affect the subject's safety.
Genitourinary diseases: presence of any specific genitourinary symptoms detected at visit 2 with the relevant questionnaire (genitourinary symptoms questionnaire).
Infection history: history of bacterial urinary tract or bacterial or fungal vaginal infections for 3 weeks before the screening visit.
Systemic and/or local infections: bacterial or fungal infections that may interfere with the aim of the study or affect the subject's safety. If the results of the microbiological analyses concerning Ureaplasma/Mycoplasma and Actinomyces are positive, the subject can be enrolled only if asymptomatic and without any clinical evidence (gynaecological visit, PAP test and vaginal pH measurement) of vaginal infections.
Gynaecological findings: clinically significant abnormal findings at the gynaecological visit performed by the study Gynaecologist.
Mucosa conditions: altered mucosa conditions affecting the site of insertion (e.g. open lesions or other).
Habits: use of vaginal detergents, soaps and washes that, in the Investigator's opinion, may have an influence on vaginal pH and/or change the vaginal flora.
Medications: any medication (topical or systemic), including over the counter, herbal medication, topical drugs on the application area, and anticoagulants, such as warfarin, acenocoumarol and rivaroxaban, for 2 weeks before the start of the study. Hormonal contraceptives and hormonal replacement therapies are allowed. Paracetamol will be allowed as a counter-measure for adverse events, on a case by case basis, if deemed appropriate by the Investigator.
Investigative drug studies: participation in the evaluation of any drug for 3 months before this study, calculated from the first day of the month following the last visit of a previous study and the first day of the present study (date of the informed consent signature).
Blood donation: blood donations for 3 months before this study.
Drug, alcohol, caffeine, tobacco: history of drug, alcohol (> 1 drink/day, defined according to USDA Dietary Guidelines 2010), tobacco (≥ 10 cigarettes/day) or caffeine (> 5 cups coffee/tea/day) abuse.
Diet: Abnormal diets (< 1600 or > 3500 kcal/day) or substantial changes in eating habits in the 4 weeks before this study; vegetarians.
Pregnancy: positive or missing pregnancy test at screening or day 1, pregnant or lactating women or females of child-bearing potential not following adequate contraceptive procedures.
Non-compliance: subjects suspected to have a high potential for non-compliance to the study procedures according to the Investigator's judgement, including non-compliance to sexual abstinence during the study.
Drug test (cocaine, amphetamine, methamphetamine, cannabinoids, opiates and ecstasy): positive result at the drug test at screening.
Alcohol test: positive alcohol breath test at day 1.