Short Incubation Methylaminolevulinate Photodynamic Therapy Without Occlusion

NCT ID: NCT00926952

Last Updated: 2011-09-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-07-31
• Study Completion Date: 2011-01-31

Brief Summary

Actinic keratoses on the face are often numerous and widespread. The application of Methylaminolevulinate (MAL) on individual lesions followed by the application of a plastic film on each lesion is difficult and takes time for subjects with many actinic keratoses. The waiting period of 3 hours between MAL cream application and red light exposure is also long for patients. The goal of this study is to evaluate the safety and efficacy of photodynamic therapy (PDT) with MAL with a shorter cream application time (90 minutes) and when MAL is applied on the entire face without the plastic film.

Detailed Description

A total of 20 patients with at least 5 non-hypertrophic actinic keratoses (AK) of the face were included in this open-label study. All AKs were mapped on a transparent template before the first PDT treatment. At Day 0, all patients received methylaminolevulinate (MAL) applied on the entire face (except the nose and peri-ocular area of 1-2 cm) without any skin preparation. One to two 2 g MAL tubes was used for the entire face. MAL was applied without occlusion. After a total of 90 +/- 5 minutes the skin was rinsed and exposed to 37 J/cm² of red light from an Aktilite™ device. Patients were seen at Week 4; if all facial AKs did not show a complete response to treatment, the MAL-PDT procedure was repeated at Week 4. Patients were seen again at Week 12 and 24.

The primary endpoint was at Week 12. Patients came back at Week 24 for a final safety evaluation and to verify the recurrence of AK.

Efficacy is evaluated by assessing the mean number of facial AK at Week 12 as compared to Day 0.

Conditions

Actinic Keratosis

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

MAL-PDT 90 min incubation, no occlusion

Patients had 2-4 g of Methylaminolevulinate (MAL) spread on the entire face without occlusion and waited 90 minutes prior to photodynamic therapy (PDT) using red light.

Group Type: EXPERIMENTAL

Methylaminolevulinate (Metvix, Metvixia)

Intervention Type: DRUG

2-4 g of cream applied to entire face at Day 0 for 90 minutes without occlusion prior to light treatment. If any actinic keratoses remained after 4 weeks the treatment was repeated at Week 4.

Photodynamic Therapy (Aktilite)

Intervention Type: DEVICE

Device set to 37 J/cm². Red light wavelength is approximately 630 nm.

Interventions

Methylaminolevulinate (Metvix, Metvixia)

2-4 g of cream applied to entire face at Day 0 for 90 minutes without occlusion prior to light treatment. If any actinic keratoses remained after 4 weeks the treatment was repeated at Week 4.

Intervention Type: DRUG

Photodynamic Therapy (Aktilite)

Device set to 37 J/cm². Red light wavelength is approximately 630 nm.

Intervention Type: DEVICE

Other Intervention Names

Metvix, Metvixia; Aktilite

Eligibility Criteria

Inclusion Criteria

• Age 18 or older.
• Patient with at least 5 actinic keratoses of the face at Day 0.
• Patient was willing to use an adequate contraceptive method or was surgically sterile, post menopausal, abstinent or with a same sex partner. Adequate means of contraception included oral contraceptives, IUD in use for 30 days before Day 0, barrier methods and spermicide in use at least 14 days before Day 0.
• Patient capable of giving informed consent.

Exclusion Criteria

• Patient with allergy to methylaminolevulinate or any component of the vehicle which includes peanut and almond oil.
• Patient with clinically significant sensitivity to visible light, porphyria or porphyrin sensitivity.
• Patient used any topical treatment for actinic keratoses (including imiquimod and 5-fluouracil), on the face within 4 weeks preceding Day 0.
• Patient had cryotherapy or surgery on the face within 4 weeks preceding Day 0.
• Patient with any malignant skin lesion (such as basal cell carcinoma, invasive squamous cell carcinoma or Bowen's disease) on the face at Day 0.
• Patient used photodynamic therapy, with any topical or systemic photosensitizer within 8 weeks preceding Day 0.
• Patient was exposed to excessive ultraviolet radiation (UVB phototherapy, sun tanning salons) within the 4 weeks preceding Day 0.
• Patient used any investigational drug within 4 weeks preceding Day 0.
• Patient with problems of alcoholism or drug abuse in the past year.
• Patient with any unstable or serious uncontrolled medical condition.
• Current pregnancy or lactation.
• Patient with any serious dermatological disorder, including malignancies that would either put the patient at risk or interfere with efficacy or safety evaluations.
• Patient with Fitzpatrick phototype IV, V or VI (inadequate penetration of red light in dark skinned subjects.
• Patients with extensive facial hair (e.g., beard) that would either impair red light exposure or interfere with lesion evaluation.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Galderma Canada

OTHER

Sponsor Role: collaborator

Innovaderm Research Inc.

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Robert Bissonnette, MD, FRCPC

Role: PRINCIPAL_INVESTIGATOR

Innovaderm Research

Locations

Innovaderm Research Inc

Montreal, Quebec, Canada

Countries

Canada

References

Griffiths CE, Wang TS, Hamilton TA, Voorhees JJ, Ellis CN. A photonumeric scale for the assessment of cutaneous photodamage. Arch Dermatol. 1992 Mar;128(3):347-51.

Reference Type: BACKGROUND

PMID: 1550366 (View on PubMed)

Other Identifiers

Inno-6010

Identifier Type: -

Identifier Source: org_study_id