Lionel ALIES

DUCRAY brand

A chemical engineer specialising in cosmetology and toxicology, Lionel ALIES designs and oversees the clinical trials carried out on the acne products produced by Laboratoires Dermatologiques Ducray. 

Drawing on his experience in the cosmetics industry and clinical evaluation, he designs testing programmes to address challenges relating to innovation, safety and product performance.

What is Lionel ALIES’s career background?

Since 2024: Clinical Evaluation Project Manager – Ducray.

2021–2024: Regulatory Project Manager in the cosmetics industry.

2013–2021: Clinical Evaluation Project Manager in the cosmetics industry.

2008–2012: Clinical Safety Research Officer for Cosmetics at a CRO.

Educational Qualifications: Chemical Engineer (2006), Master’s degree in Industrial Cosmetology (2007) and University diploma in Toxicology (2011).

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What is his role within the DUCRAY brand? 

Lionel ALIES ensures that clinical assessments are relevant and robust. His role centres on:

  • the design and coordination of clinical trials: in collaboration with Pierre Fabre’s in-house dermatologists and national and international CROs, he designs and coordinates clinical trials using tailored and innovative evaluation protocols, in order to validate the safety and demonstrate the efficacy of DUCRAY skincare products for problem skin.
  • Dissemination & Scientific Communication: he promotes the results of clinical trials through scientific presentations and posters.
  • Scientific monitoring and regulatory compliance: He actively monitors developments in evaluation techniques, scientific and medical practices, and cosmetic standards and guidelines, in order to design studies that set the company apart whilst ensuring their relevance, credibility and compliance.

A WORD FROM THE EXPERT

My role is to design and lead evaluation programmes to ensure that every Ducray product innovation is underpinned by indisputable and innovative clinical data on tolerability and efficacy.

Lionel ALIES

Clinical Evaluation Officer

Scientific papers

    Frequently asked questions about clinical trials?

    A clinical evaluation involves verifying, in humans, that our products are well tolerated under medical supervision, either under conditions designed to maximise their effects or under normal conditions of use, as well as assessing their efficacy.
    It is carried out in several stages. Following validation of the skin and eye compatibility of our formulations using in vitro (cell-based) models, our products are then applied to women and men in accordance with clearly defined and standardised protocols.

    The effectiveness of our treatments is measured using rating scales and quality-of-life questionnaires recognised within the dermatological community, as well as through instrumental measurements and image analysis, which enable us to assess, with a high degree of precision, changes in skin condition in terms of blemishes, sebum, hydration, etc.

    Clinical trials contribute to product innovation at DUCRAY by introducing new approaches to the assessment of the clinical signs of the skin conditions under investigation, in collaboration with our Medical and Research departments, and by utilising our trial results in different ways to develop innovative, unique products that meet the needs of our patients and healthcare professionals.