A Multi-center, Double-blind, Randomized Study, Comparing Clindamycin Phosphate Vaginal Cream 2% (Watson Laboratories, Inc.) to Clindesse® (Ther-Rx™, Clindamyin Phosphate Vaginal Cream 2%) and Both Active Treatments to a Placebo Control in the Treatment of Bacterial Vaginosis in Non-pregnant Women

BACTERIAL VAGINOSIS Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02210689
• Other study ID #: 13-1052
• Status: Completed
• Phase: Phase 3
• Start date: January 2014
• Est. completion date: December 2014

Study information

• Verified date: January 2020
• Source: Actavis Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A multi-center, double-blind, randomized, placebo controlled, parallel-group study, comparing Clindamycin phosphate vaginal cream 2% (Watson Laboratories, Inc.) to Clindesse® (Ther-Rx™, Clindamyin Phosphate Vaginal Cream 2%) and both active treatments to a placebo control in the treatment of bacterial vaginosis in non-pregnant women.

Description:

The study treatment period will be 1 day. Subject participation is 22-30 days. Expected study duration is 10 to 12 months. The study will enroll in up to 30 clinical sites.

Test Product: One single-dose, pre-filled disposable applicator delivering approximately 5 g of cream containing approximately 100 mg of clindamycin phosphate vaginal cream 2% (Watson Laboratories, Inc.)

Reference Product: One single-dose, pre-filled disposable applicator delivering approximately 5 g of cream containing approximately 100 mg of Clindesse® (clindamycin phosphate vaginal cream 2% ) (Ther-Rx™)

Placebo Control: One single-dose, pre-filled disposable applicator delivering approximately 5 g of cream containing vehicle of the test product (Watson Laboratories, Inc.)

Dose and Mode A single applicator of investigational product cream will be administered of Administration once intravaginally at any time of the day. The subject participation is 22-30 days (drug administration for 1 day).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 604
• Est. completion date: December 2014
• Est. primary completion date: October 2014
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Subjects must be willing and able to understand and comply with the requirements of the protocol, including attendance at the required study visits and must provide the written informed consent prior to any study related procedure being performed.

2. Healthy non-pregnant female aged = 18 years with no known medical conditions that, in the investigator's opinion, may interfere with study participation or may interfere with the evaluation of bacterial vaginosis.

3. Female subjects of childbearing potential (excluding women who are surgically sterilized or postmenopausal for at least 1 year), in addition to having a negative urine pregnancy test must be willing to use an acceptable form of birth control during the study from the day of the first dose administration to the Visit 2 Test-of-cure. For the purpose of this study the following are considered acceptable methods of birth control:

• Oral or injectable contraceptives

• Contraceptive patches

• Depo-Provera® (stabilized for at least 3 months); Implanon™ (contraceptive implant), or abstinence with one of the above-listed methods of birth control should the Subject become sexually active.

• A sterile sexual partner is NOT considered an adequate form of birth control.

• Willing to refrain from sexual intercourse on study days 1-7 and for 48 hours prior to Visit 2 Test-of-cure.

4. Willing to refrain from using any vaginal product (e.g., spermicide, tampon, douche, diaphragm, or condom) other than study product, on study Days 1-7, for 48 hours prior to the first dose of study product, and for 48 hours prior to Visit 2 Test-of-cure.

5. Diagnosis of bacterial vaginosis, defined as the presence of all of the following:

• Clinical diagnosis of bacterial vaginosis (e.g., thin, homogenous vaginal discharge associated with minimal or absent pruritus or inflammation AND

• Saline wet mount of vaginal discharge demonstrating the proportion of clue cell to be = 20% of the total epithelial cells AND

• Vaginal pH > 4.5, using pH paper that measures from 4.0-6.0 AND

• Positive "whiff test" after addition of a drop of 10% KOH to vaginal discharge)

• Gram stain Nugent score = 4 on first day of dosing (study day 1) (per Table 1 below).

• Table 1: Nugent Scoring System (0-10) for Gram-stained Vaginal Smears (a)

• Score (b) Lactobacillus morphotypes Gardnerella and Bacteroides spp. morphotypes Curved gram-variable rods

• 0 4+ 0 0

• 1 3+ 1+ 1+ or 2+

• 2 2+ 2+ 3+ or 4+

• 3 1+ 3+

• 4 0 4+

Source: Nugent, R. P., M. A. Krohn, and S. L. Hillier. Reliability of diagnosing bacterial vaginosis is improved by a standardized method of Gram stain interpretation. J. Clin. Microbial. 1991; 29: 297-301.

• Morphotypes are scored as the average number seen per oil immersion field. Note that less weight is given to curved gram-variable rods. Total score = lactobacilli + G. vaginalis and Bacteroides spp/ + curved rods.

• 0, No morphotypes present; 1, <1 morphotype present; 2, 1 to 4 morphotypes present; 3, 5 to 30 morphotypes present; 4, 30 or more morphotypes present.

Exclusion Criteria:

1. Female subjects who are pregnant, nursing or planning to become pregnant during study participation.

2. Menstruating when diagnosis of bacterial vaginosis is determined at Baseline visit.

3. Primary or secondary immunodeficiency.

4. Severe liver disease.

5. History of regional enteritis, ulcerative colitis, or a history of "antibiotic-associated" colitis.

6. Evidence of any vulvovaginitis other than bacterial vaginosis. (e.g., candidiasis, Trichomonas vaginalis, Chlamydia trachomatis, Neisseria gonorrhoeae, Herpes simplex).

7. Subjects with visible signs of HPV infection, i.e. visible warts.

8. Subject with another vaginal or vulvar condition, which would confound the interpretation of clinical response.

9. Subject will be under treatment during the study period for cervical intraepithelial neoplasia (CIN) or cervical carcinoma.

10. History of hypersensitivity to clindamycin, lincomycin, or any of the components of the vaginal creams.

11. Use within 2 weeks prior to baseline of 1) topical or systemic antibiotics or 2) topical or systemic antifungal.

12. Use of spermicides, tampons, douches, diaphragms, condoms within 48 hours of the baseline visit.

13. Concurrent use of systemic corticosteroids or systemic antibiotics.

14. Unwilling or unable to comply with the protocol requirements.

15. Subjects who have participated in an investigational drug study (i.e., subjects have been treated with an investigational drug) within 30 days prior to baseline will be excluded from study participation. Subjects who are participating in non-treatment studies such as observational studies or registry studies can be considered for inclusion.

16. Subjects who have been previously enrolled in this study.

Related Conditions & MeSH terms

• BACTERIAL VAGINOSIS
• Inflammation
• Signs and Symptoms
• Signs and Symptoms to be Evaluated and Recorded Include
• Vaginal Discharge
• Vaginal Discharge Color, Odor, and Consistency
• Vaginal Diseases
• Vaginosis, Bacterial
• Vulvovaginal Inflammation (Objective) Absent, Mild, Moderate, or Severe
• Vulvovaginal Itching and Irritation (Subjective) Absent, Mild, Moderate, or Severe

Intervention

Drug:
• clindamycin phosphate vaginal cream 2%

Other:
• placebo
vehicle used as placebo

Locations

Country	Name	City	State
Dominican Republic	Akesis investigator site 3	Santo Domingo	Republica Dominicana
Dominican Republic	Akesis investigator site 4	Santo Domingo	Republica Dominicana
Puerto Rico	Akesis Investigator site 2	Ponce
United States	Akesis Investigator site 5	Birmingham	Alabama
United States	Akesis Investigator site 1	Boynton Beach	Florida
United States	Akesis investigator site 18	Houston	Texas
United States	Akesis Investigator site 7	Jackson	Tennessee
United States	Akesis Investigator site 12	La Mesa	California
United States	Akesis investigator site 16	Lawrenceville	New Jersey
United States	Akesis Investigator site 15	Metairie	Louisiana
United States	Akesis investigator site 14	North Miami	Florida
United States	Akesis investigator site 13	Philadelphia	Pennsylvania
United States	Akesis investigator site 11	Port Jefferson	New York
United States	Akesis Investigator site 9	Roswell	Georgia
United States	Akesis investigator site 6	San Diego	California
United States	Akesis investigator site 17	Sanford	Florida
United States	Akesis investigator site 8	Sunrise	Florida
United States	Akesis Investigator site 10	West Palm Beach	Florida

Sponsors (2)

Lead Sponsor	Collaborator
Actavis Inc.	Watson Laboratories, Inc.

Countries where clinical trial is conducted

United States,  Dominican Republic,  Puerto Rico, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants With Both a Clinical and a Bacteriological Cure (Nugent Score <4), Evaluated at Visit 2 Test-of-cure (Study Day 22-30).	Clinical Cure is defined as resolution of clinical signs and symptoms from entry visit as follows: The original discharge characteristic of bacterial vaginosis has returned to a normal physiological vaginal discharge which varies in appearance and consistency depending on the menstrual cycle,; The whiff test is negative for any amine ("fishy") odor,; The saline wet mount is negative for clue cells,; Vaginal fluid pH is < 4.7, using pH paper that measures from 3.6 to 6.1.; A Bacteriological cure is defined as a Nugent score < 4.; The system used a 0-4 scale (Nugent Scoring System 0-10 for Gram-Stained Vaginal Smears) for evaluation of vaginal flora, based on the weighted sum of the following 3 bacterial morphotypes scores calculated from slide examination under oil immersion field: Lactobacillus: large gram positive rods,; Gardnerella / Bacteroides spp: Small gram variable coccobacilli/small Gram negative rods,; Mobiluncus spp.: thin, curved Gram variable rods	22 to 30 days