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Clinical Trials/EUCTR2007-000232-12-GB
EUCTR2007-000232-12-GB
Active, not recruiting
Not Applicable

ovel topical therapies for acne vulgaris: a randomised, controlled, double blind comparison of the antibacterial efficacy of 1% w/v formulations of tert-butylhydroquinone, zinc pyrithione and benzoyl peroxide in healthy volunteers - Antibacterial efficacy of novel topical therapies for acne

Syntopix Group plc0 sitesJanuary 28, 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy volunteer study. The product under development will be used for the treatment of acne vulgaris.
Sponsor
Syntopix Group plc
Status
Active, not recruiting
Last Updated
14 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 28, 2007
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Male

Investigators

Sponsor
Syntopix Group plc

Eligibility Criteria

Inclusion Criteria

  • \- age 16 \- 50 years
  • \- in good health
  • \- Caucasian
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range
  • F.1\.3 Elderly (\>\=65 years) no
  • F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • \- any skin disease affecting the upper back
  • \- history of allergy or suspected allergy to any of the test substances
  • \- taking any regular treatment via the systemic route
  • \- use of any topical skin care preparations on the back or anti\-bacterial skin care preparations at any site
  • \- any chronic medical condition that oculd affect drug handling by the skin, liver or kidneys
  • \- positive result in abbreviated drug screen
  • \- unwilling or unable to attend appointments on 15 consecutive days

Outcomes

Primary Outcomes

Not specified

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