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Development of a non-invasive skin diagnostic test for guiding vi | 7714
Journal of Clinical & Experimental Dermatology Research

Journal of Clinical & Experimental Dermatology Research
Open Access

ISSN: 2155-9554

+44 1478 350008

Development of a non-invasive skin diagnostic test for guiding vitiligo treatment


Vitiligo and Skincare Physicians Meeting

September 15-16, 2016 Berlin, Germany

Pieter Spee

FibroTx LLC, Estonia

Scientific Tracks Abstracts: J Clin Exp Dermatol Res

Abstract :

Vitiligo is a chronic and as yet incurable disease characterized by depigmentation of skin. Disease progression often follows the typical pattern of disease-active periods that are alternated by periods of relative stability. There are no specific treatments for vitiligo, with the exception of skin transplantation, which success critically depends on stable disease to avoid depigmentation of transplanted skin. Treatments for active disease typically suppress inflammation, a critical component of vitiligo pathology, with the aim to inhibit the expansion of skin lesions. Treatment options include steroids, calcineurin inhibitors, as well as phototherapy, which only have effect on active disease, but not on stable disease. Although the status of disease activity is an important parameter for treatment decision-making, assessment of disease activity remains difficult. Either, dermatologists monitor the expansion of lesions, a rather lengthy process or dermatologists rely on patient testimonies. Both methods have proven unsatisfactory and thus there is an unmet medical need for diagnostic tools that can monitor disease activity to guide disease management. FibroTx TAP and SELF are novel molecular diagnostic platform technologies that can measure protein biomarkers directly from skin. These non-invasive platform technologies are currently being tested in clinical studies for the development of a skin diagnostic tool that can assess the activity status of skin lesions of vitiligo patients. The aim of the studies is to develop the first point-of-care device that can markedly improve vitiligo treatment, which is cost-efficient and does not require the need for clinical laboratory expertise.

Biography :

Pieter Spee has completed his PhD at the Graduate School of Oncology at the Netherlands Cancer Institute and the University of Leiden in the Netherlands. He has worked 11 years at Novo Nordisk as the Director and Scientific Director of Translational Immunology where he made significant contributions to Lirilumab and Monalizumab, currently in clinical development for various cancers. Presently, he serves as a Chief Technology Officer of FibroTx where he brought the noninvasive biomarker test FibroTx TAP to the market and where he oversees the clinical development of FibroTx SELF, a non-invasive skin diagnostic test intended as point-of-care device for catering personalized skin treatment.

Email: pieter.spee@yahoo.dk

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