Safety and Tolerability of Antiplaque Chewing Gum in a Gingivitis Population (APCG)

United States Army Medical Research and Development Command (USAMRDC)

Status and phase

Completed

Phase 2

Phase 1

Conditions

Plaque

Gingivitis

Treatments

Drug: 20 mg KSL-W

Other: Placebo

Drug: 50 mg KSL-W

Drug: 100 mg KSL-W

Drug: 4 mg KSL-W

Drug: 2 mg KSL-W

Drug: 30 mg KSL-W

Drug: 6 mg KSL-W

Drug: 75 mg KSL-W

Drug: 10 mg KSL-W

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT01877421

S-11-14

Details and patient eligibility

About

This study is to assess the safety and tolerability of single doses and multiple doses in reducing plaque and gingivitis when delivered in a chewing gum formulation.

Full description

This study is a Phase 1/2a placebo-controlled, double-blind, randomized, dose-escalation study to evaluate the safety and proof of concept of Antiplaque Chewing Gum. This is a 2-part trial with 9 dosing cohorts in Phase 1 and 7 dosing cohorts in Phase 2a. For both phases, the oral soft (OST) and oral hard tissues (OHT) will be examined. Changes from baseline, such as soft tissue erythema, ulceration and sloughing, will be noted and assessments will be made by the principal investigator as to whether they might be attributable to the antiplaque chewing gum.

In the Phase 2a portion of the study, the efficacy of the antiplaque chewing gum in reducing existing supragingival plaque and gingivitis will also be assessed. Plaque will be assessed using the Turesky Modification of the Quigley-Hein Plaque Index (PI, Turesky et al-1970) and gingivitis will be assessed using both the Modified Gingival Index (MGI, Lobene et al-1986) and the percent of bleeding sites on gentle probing (BOP) using the methods described in Ainamo and Bay-1975.

Enrollment

135 patients

Sex

All

Ages

18 to 64 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Subjects must meet all of the following criteria to be included in the Phase 1 portion of the study:

Males and females between 18 and 64 years of age
A negative urine pregnancy test and willingness to use a reliable form of contraception for the duration of the study (females of childbearing potential only), with reliable contraception defined as:

Abstinence Oral contraceptive, either estrogen progesterone combined, or progesterone alone Injectable progesterone Implants of levonorgestrel Estrogenic vaginal ring Percutaneous contraceptive patches Intrauterine device or intrauterine system Double barrier method [condom or occlusive cap (diaphragm or cervical vault caps) plus spermicidal agent (foam, gel, film, cream, suppository)] Male partner sterilization prior to the female subject's entry into the study, and this male is the sole partner for that subject

Good health, as determined by pertinent medical history, physical examination, vital signs, and clinical safety laboratory evaluations
A minimum of 16 natural teeth with 2 scorable surfaces (facial and lingual) per tooth Sufficient number of opposing posterior teeth to chew on both sides of the mouth as determined by the examining dentist Teeth that have gross caries, full crowns or extensive restorations on facial and/or lingual surfaces, orthodontic bands, and third molars are not included in the tooth count
Ability to comprehend and a willingness to sign an informed consent, which includes the Authorization for the Release of Health Information document
Willingness to comply with all study procedures

Phase 2a Inclusion Criteria

Subjects must meet all the criteria for the phase 1 portion of the study, and in addition must:

Have mild to moderate gingivitis and plaque MGI of 1.8 or greater (Ainamo and Bay-1975) PI of 1.95 or greater (Turesky et al-1970)
Willing to forgo any optional dental procedures during the study period, such as dental prophylaxis or teeth whitening

Exclusion criteria

Subjects meeting any of the following criteria will be excluded from the study:

Acute or chronic medical conditions, organ system disease, or medications that, in the principal investigator's opinion, would impair the subject's ability to participate
TMD
Self-reported use of tobacco products
Use of anticoagulant medications (eg clopidogrel)
Gross oral pathology, including widespread caries or chronic neglect, extensive restoration, pre-existing gross plaque or calculus, or soft or hard tissue tumor of the oral cavity
Orthodontic appliances or removable partial dentures that will compromise the ability of the potential subject to participate in the study
Periodontitis as indicated periodontal pockets greater than 4 millimeters on more than one site
Receipt of any investigational drug/test product within 30 days prior to study entry
Receipt of antibiotics within 30 days prior to study entry
Need for antibiotic prophylaxis prior to invasive dental procedures
Receipt of daily anti-inflammatory therapy [eg nonsteroidal anti-inflammatory drugs (NSAID), tumor necrosis factor (TNF) alpha blockers] within 30 days prior to study entry
Receipt of prescription antibacterial oral products (eg products containing chlorhexidine) within 30 days prior to study entry
Pregnant or breast-feeding female
Clinically significant abnormal laboratory tests as determined by the principal investigator
An employee of the study site directly involved with the study
Inability to comply with assigned treatment regimen

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

135 participants in 10 patient groups, including a placebo group

2 mg KSL-W (Phase 1, 1a)

Experimental group

Description:

one 2 mg KSL-W tablet at day 0 at Phase 1

Treatment:

Drug: 2 mg KSL-W

4 mg KSL-W (Phase 1, 2a; Phase 2a, 1b)

Experimental group

Description:

one 4 mg KSL-W tablet on day 0 at both Phase 1 and Phase 2a. one 4 mg KSL-W tablet on days 1-6; two 4 mg KSL-W tablets on days 7-13 and days 14-20; and three 4 mg tablets at days 21-27 at Phase 2a.

Treatment:

Drug: 4 mg KSL-W

6 mg KSL-W (Phase 1, 3a; Phase 2a, 2b)

Experimental group

Description:

One 6 mg KSL-W tablet on day 0 at both Phase 1 and Phase 2a. One 6 mg KSL-W tablet on days 1-6; two 6 mg KSL-W tablets on days 7-13 and days 14-20; and three 6 mg tablets at days 21-27 at Phase 2a.

Treatment:

Drug: 6 mg KSL-W

10 mg KSL-W (Phase 1, 4a; Phase 2a, 3b)

Experimental group

Description:

One 10 mg KSL-W tablet on day 0 at both Phase 1 and Phase 2a. One 10 mg KSL-W tablet on days 1-6; two 10 mg KSL-W tablets on days 7-13 and days 14-20; and three 10 mg tablets at days 21-27 at Phase 2a.

Treatment:

Drug: 10 mg KSL-W

20 mg KSL-W (Phase 1, 5a; Phase 2a, 4b)

Experimental group

Description:

One 20 mg KSL-W tablet on day 0 at both Phase 1 and Phase 2a. One 20 mg KSL-W tablet on days 1-6; two 20 mg KSL-W tablets on days 7-13 and days 14-20; and three 20 mg tablets at days 21-27 at Phase 2a.

Treatment:

Drug: 20 mg KSL-W

30 mg KSL-W (Phase 1, 6a; Phase 2a, 5b)

Experimental group

Description:

One 30 mg KSL-W tablet on day 0 at both Phase 1 and Phase 2a. One 30 mg KSL-W tablet on days 1-6; two 30 mg KSL-W tablets on days 7-13 and days 14-20; and three 30 mg tablets at days 21-27 at Phase 2a.

Treatment:

Drug: 30 mg KSL-W

50 mg KSL-W (Phase 1, 7a; Phase 2a, 6b)

Experimental group

Description:

One 50 mg KSL-W tablet on day 0 at both Phase 1 and Phase 2a. One 50 mg KSL-W tablet on days 1-6; two 50 mg KSL-W tablets on days 7-13 and days 14-20; and three 50 mg tablets at days 21-27 at Phase 2a.

Treatment:

Drug: 50 mg KSL-W

75 mg KSL-W (Phase 1, 8a; Phase 2a, 7b)

Experimental group

Description:

One 75 mg KSL-W tablet on day 0 at both Phase 1 and Phase 2a. One 75 mg KSL-W tablet on days 1-6; two 75 mg KSL-W tablets on days 7-13 and days 14-20; and three 75 mg tablets at days 21-27 at Phase 2a.

Treatment:

Drug: 75 mg KSL-W

100 mg KSL-W (Phase 1, 9a)

Experimental group

Description:

one 100 mg KSL-W tablet at day 0 at Phase 1

Treatment:

Drug: 100 mg KSL-W

Placebo

Placebo Comparator group

Description:

Placebo