A Study to Investigate the Anti-Plaque Effect of AN0128 Toothpaste

This study has been completed.
Sponsor:
Information provided by:
Anacor Pharmaceuticals, Inc.
ClinicalTrials.gov Identifier:
NCT00762151
First received: September 24, 2008
Last updated: September 29, 2008
Last verified: September 2008

September 24, 2008
September 29, 2008
November 2007
January 2008   (final data collection date for primary outcome measure)
Reduction in the gingival margin plaque index in a 24-hour post-treatment (no brushing) [ Time Frame: Baseline (time zero), 24 hour time point ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00762151 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
A Study to Investigate the Anti-Plaque Effect of AN0128 Toothpaste
Clinical Research Study to Investigate the Anti-Plaque Effect of a Prototype Toothpaste Containing an Anacor Material Via the MGMPI Method

The objective of this study was to evaluate the anti-plaque efficacy of the Anacor prototype dentrifice as compared to commercial control products following a single use of the dentrifice.

The widespread successful use of triclosan as an anti-inflammatory and anti-bacterial agent is well documented. The standard dentrifice has demonstrated a robust anti-plaque and anti-inflammatory effect providing multiple benefits. There is a clear value to identify additional agents with the same dual action with a comparable or an enhanced level of efficacy. This study examined the anti-plaque efficacy following a single use of the prototype dentifrice.

Interventional
Phase 1
Endpoint Classification: Efficacy Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Prevention
Dental Plaque
  • Other: Negative Control (Regular Toothpaste)
    Regular Toothpaste
  • Other: Positive Control (anti-plaque/anti-bacterial toothpaste)
    Standard anti-plaque and anti-bacterial toothpaste
  • Other: Prototype (AN0128 Toothpaste)
    AN0128 Toothpaste
  • Placebo Comparator: Negative Control
    Regular Toothpaste
    Intervention: Other: Negative Control (Regular Toothpaste)
  • Active Comparator: Positive Control
    Standard anti-plaque and anti-bacterial toothpaste.
    Intervention: Other: Positive Control (anti-plaque/anti-bacterial toothpaste)
  • Active Comparator: Prototype
    AN0128 Toothpaste
    Intervention: Other: Prototype (AN0128 Toothpaste)
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
18
January 2008
January 2008   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Must be between ages 18 to 65 years inclusive
  • Have a minimum of 16 natural uncrowned teeth (excluding 3rd molars) present
  • Must give written informed consent
  • Be in good general health
  • Must discontinue oral hygiene for 24-hours after initial appointment
  • No known history of allergy to personal care/consumer products or their ingredients, relevant to any ingredient in the test products as determined by the dental/medical professional monitoring the study

Exclusion Criteria:

  • Medical condition which requires pre-medication prior to dental visits/procedures
  • Advanced periodontal disease
  • 5 or more decayed, untreated dental sites
  • Diseases of the soft or hard oral tissues
  • Orthodontic appliances
  • Abnormal salivary function
  • Use of drugs that can affect salivary flow
  • Use of antibiotics one (1) month prior to or during this study
  • Use of any over the counter medications other than analgesics (i.e. aspirin, ibuprofen, acetaminophen, naproxen), unless approved by the study medical staff
  • Pregnant or breastfeeding
  • Participation in another clinical study in the month preceding this study
  • Allergic to common dentifrice ingredients
  • Immune compromised individuals (HIV, AIDS, immuno suppressive drug therapy)
  • History of allergic reaction to any anti-inflammatory agents
Both
18 Years to 65 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00762151
AN0128 Periodontal Plaque
No
Kirk R Maples, PhD, Anacor Pharmaceuticals, Inc.
Anacor Pharmaceuticals, Inc.
Not Provided
Study Director: Kirk R Maples, PhD Anacor Pharmaceuticals, Inc.
Anacor Pharmaceuticals, Inc.
September 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP