Roxane Castan

Roxane Castan has extensive experience in regulatory affairs and clinical trials management, currently serving as the Manager of Clinical Trials Regulatory at DBV Technologies since May 2025, where responsibilities include coordinating regulatory submissions for Phase 3 clinical trials and developing project timelines. Prior roles at DBV Technologies include a Project Manager position in Regulatory Affairs for Phase 3 clinical trials focused on an investigational treatment for peanut allergy. Roxane's background also includes an apprenticeship in regulatory affairs at Vetoquinol Global, and previous experience in peptide synthesis and organic chemistry projects during studies in chemical engineering and natural products chemistry. Educational credentials include a Master's degree from Ecole Nationale Supérieure de Chimie de Montpellier and a Bachelor's from Université du Québec à Chicoutimi, complemented by international study at Linköping University and a technical degree from IUT MONTPELLIER-SETE.