Safety and Efficacy Study of Topical Methyaminlevulinate (MAL) in Subjects With Facial Acne

A Study of Safety and Efficacy of Topical Methylaminolevulinate 80mg/g With and Without Occlusion Followed by Red Light Exposure in Subjects With Facial Acne

A study of safety and efficacy of topical methyaminlevulinate 80mg/g with and without occlusion followed by red light exposure in subjects with facial acne.

Study Overview

• Status: Completed
• Conditions: Acne
• Intervention / Treatment: Drug: MAL

Detailed Description

Photocure ASA has developed a cream formulation containing methyl aminolevulinate (MAL), an ester of ALA. There is extensive experience with the safety of MAL-PDT in humans.

This study will assess safety and efficacy of four treatments with methylaminolevulinate (MAL) at 80 mg/g performed with and without occlusion and followed by red light exposure 90 minutes later in subjects with facial acne vulgaris. Subjects will be randomized to one of two groups of 20 subjects: Group 1 will receive 25 J/cm2 of red light (45 mW/cm2) and group 2 will receive 37 J/cm2 of red light (90 mW/cm2). For each subject one side of the face will be randomized to receive MAL for 90 minutes without occlusion and the other side of the face will receive MAL for 90 minutes with occlusion.

• Study Type: Interventional
• Enrollment (Actual): 44
• Phase: Phase 2

Contacts and Locations

Study Locations

• Canada
  • Quebec
    • Laval, Quebec, Canada, H7S 2C6
      • Innovaderm Research Inc
    • Montreal, Quebec, Canada, H2K 4L5
      • Innovaderm Research Inc.

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Subject willing to use an adequate contraceptive method or is surgically sterile, post menopausal, abstinent or with a same-sex partner. Adequate means of contraception include; IUD in use 30 days prior to day 0, barrier methods and spermicide in use atleast 14 days prior to day 0 or oral contraceptive in use for at least 6 months prior to day 0
• Age 18 or older
• Capable of giving informed consent
• Diagnosis of acne vulgaris on the face with at least 10 inflammatory lesions on both sides of the face at screening and day 0
• Global acne severity assessment score ≥ 3 at the screening and day 0 visit.

Exclusion Criteria:

• Allergy to methylaminolevulinate or any component of the vehicle
• Acne fulminans or conglobata on the face
• Clinical significant sensitivity to visible light, porphyria or porphyrin sensitivity
• Use of any topical treatment for acne on the face within the previous 2 weeks before day 0
• Any use of systemic antibiotics within 1 month prior to day 0 or use of isotretinoin within 1 year prior to Day 0
• Exposure to ultraviolet radiation (UVB phototherapy, sun tanning salons) within 4 weeks of Day 0
• Use of any investigational drug within 4 weeks of Day 0
• Alcoholism or drug abuse in the past year
• Any unstable or serious medical condition at the discretion of the investigator
• Current pregnancy or lactation
• Use of hormonal contraceptives solely for control of acne
• Current use of oral contraceptives (unless subject is on a stable dose e.i. at least six months of treatment prior Day 0), testosterone or any other systemic hormonal treatment
• Any serious dermatological disorder, including malignancies that would either put the subject at risk or interfere with efficacy or safety evaluations
• Fitzpatrick phototype V or VI (inadequate penetration of red light in dark skin subjects)
• Subjects with extensive facial hair (e.g. beard) that would either impair red light exposure or interfere with lesion evaluation.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

4

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: 25 J/cm2, with occlusion on right side; Subjects will receive MAL cream in a thin layer on both sides of the face (except nose and peri-ocular area) at a concentration of 80 mg/g). Occlusion will be applied to one half of the face. After an incubation time of 90 minutes both sides of the face will be exposed to either 25 J/cm2 of red light starting with the occluded side first.	Drug: MAL; 80 mg/g cream one administration with incubation for 90 minutes
Active Comparator: 37 J/cm2, with occlusion on right side; Subjects will receive MAL cream in a thin layer on both sides of the face (except nose and peri-ocular area) at a concentration of 80 mg/g). Occlusion will be applied to one half of the face. After an incubation time of 90 minutes both sides of the face will be exposed to 37 J/cm2 of red light starting with the occluded side first.	Drug: MAL; 80 mg/g cream one administration with incubation for 90 minutes
Active Comparator: 25 J/cm2 , with occlusion on left side; Subjects will receive MAL cream in a thin layer on both sides of the face (except nose and peri-ocular area) at a concentration of 80 mg/g). Occlusion will be applied to one half of the face. After an incubation time of 90 minutes both sides of the face will be exposed to either 25 J/cm2 of red light starting with the occluded side first.	Drug: MAL; 80 mg/g cream one administration with incubation for 90 minutes
Active Comparator: 37 J/cm2 , with occlusion on left side; Subjects will receive MAL cream in a thin layer on both sides of the face (except nose and peri-ocular area) at a concentration of 80 mg/g). Occlusion will be applied to one half of the face. After an incubation time of 90 minutes both sides of the face will be exposed to 37 J/cm2 of red light starting with the occluded side first.	Drug: MAL; 80 mg/g cream one administration with incubation for 90 minutes

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
To compare the number of inflammatory acne lesions according to time on the side with occlusion and the side without occlusion for subjects with facial acne vulgaris exposed to 25 J/cm2 and 37 J/cm2 of red light.	4 and 12 weeks after last PDT session.

Secondary Outcome Measures

Outcome Measure	Time Frame
Exposed to 25 J/cm2 and 37 J/cm2 of red light and with and withut occlusion :-Compare number of non-inflammatory acne lesions. -Safety assesment of MAL-PDT. -Evaluate PAP photobleaching.	At each treatment visit and 2 and 7 days after first PDT treatment visit.

Collaborators and Investigators

• Sponsor: Photocure
• Investigators: Principal Investigator: Robert Bissonnette, MD MSC FRCPC, Innovaderm Research Inc.

Study record dates

Study Major Dates

• Study Start: July 1, 2007
• Primary Completion (Actual): July 1, 2008
• Study Completion (Actual): July 1, 2008

Study Registration Dates

• First Submitted: January 29, 2009
• First Submitted That Met QC Criteria: January 29, 2009
• First Posted (Estimate): January 30, 2009

Study Record Updates

• Last Update Posted (Estimate): January 30, 2009
• Last Update Submitted That Met QC Criteria: January 29, 2009
• Last Verified: January 1, 2009

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Skin Diseases; Acneiform Eruptions; Sebaceous Gland Diseases; Acne Vulgaris
• Other Study ID Numbers: INNO-6005