Efficacy and Tolerability of Topical Rossoseq™ Compared to Vehicle in Rosacea Subtype 1 (Erythematotelangiectatic)

PBB Entrepreneur

Status: Completed

Conditions: Rosacea Subtype 1 (Erythematotelangiectatic)

Treatments: Device: Rossoseq™; Device: Placebo

Study type: Interventional

Funder types: Industry

Identifiers

NCT01666509

CL-068-IV-01

Details and patient eligibility

About

Rossoseq™ is registered for the treatment of inflammatory skin conditions. Rosacea is one such inflammatory skin disorder that has not been studied yet for the use of Rossoseq™. Whilst rosacea is showing features of an inflammatory skin disorder [1], particularly stage 1 is poorly understood and treatment options are limited and therefore this study - within the target indication - will contribute to the learning about rosacea.

Full description

Male or female subjects ≥18 and < 85 years with a clinically diagnosed rosacea subtype 1 (erythematotelangiectatic) defined by a score of 6-15 for the primary and secondary features of the rosacea standard grading system (RSGS; Wilkin et al, 2004) will be enrolled.

The study will consist of a Screening visit, Baseline visit (Week 0), a telephone call at Week 1, visits at Week 2 and 4, and a follow-up telephone call at Week 5. Eligible subjects may or may not be using medication for their rosacea at the time of screening. Subjects with concomitant use of rosacea treatments will be taken off their current medication and will return for a Baseline Visit at the end of the wash-out period.

Eligible subjects will be stratified by gender at a ratio of 4:1 (Female: Male). Within the strata, subjects will be randomised at Baseline in a 2:1 ratio in favour of Rossoseq™ to receive either Rossoseq™ or vehicle.

Efficacy will be evaluated using subject rating of the rosacea specific quality of life instrument (R-QOL; Nicholson et al, 2007) during office visits and applied over the phone during the week 1 and follow-up telephone call at Week 5. An investigator rating will be performed using a "0=absent" to "3=severe" grading of the RSGS primary features flushing, nontransient erythema, papules and pustules, telangiectasia and the secondary features burning or stinging, plaques, dry appearance, edema, ocular manifestations and phymatous changes during the office visits. Ocular manifestations and phymatous changes need to be absent to be eligible for the study.

Photographs to document treatment effects will be taken at screening, baseline, week 2 and week 4.

Enrollment: 61 patients

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Signed and dated informed consent prior to any study-mandated procedure
• Clinically diagnosed rosacea defined by a score of ≥6 and ≤15 out of a maximum score of 30 for the primary and secondary features of the RSGS
• Female subjects of childbearing potential must be using appropriate birth control

Main exclusion Criteria:

• Pregnancy or lactation
• Women with the following menopausal symptoms within the last two years prior to screening: excessive sweating, flushing, mood changes
• Ocular manifestations of rosacea
• Peripheral location(s) of rosacea
• Phymatous changes
• Severe facial skin dryness or xerosis
• Keratoconjunctivitis sicca
• Flushing due to conditions other than rosacea
• Any other abnormal facial skin conditions, e.g., eczema, perioral dermatitis, broken and bleeding skin on area of application
• Malignancy within the past 2 years with the exception of in situ removal of basal cell carcinoma

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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61 participants in 2 patient groups, including a placebo group

Rossoseq™

Experimental group

Description:

Gel, topically applied twice daily

Treatment:

Device: Rossoseq™

Vehicle

Placebo Comparator group

Description:

Gel, topically applied twice

Treatment:

Device: Placebo