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Patrick Garrouste

Directeur Exécutif @Debiopharm

Martigny, CH
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Jan 2023 — Present

Directeur Exécutif @Debiopharm

CH

Management of a multidisciplinary team dedicated to oncology and antibiotic field. Our research is focused on : Drug Improvement, Drug Delivery and Drug Targeting. Competences of the team :Drug Research : medicinal chemistry and root scoutingResearch & Development : cover PLGA based drug delivery of API and solving problems of Bioavability of BCS class II API (nanosizing, solid disperson, lipidic formulation.)Analytical & Bio Research : drug substance and drug product characterization (physico-chemical and biological)Development of proprietary technologies for ADC (MultilinkTM and AbYlinkTM)

EDUCATION

2018 — 2018

IMD

Driving Strategic Innovation

1995 — 1998

University of Lausanne - UNIL

Post-Doc, chemoselective ligation of peptides

1984 — 1995

University of Montpellier

Ph D Thesis, master in biochemistry and Thesis in bio-organic chemistry (peptide and pseudopeptide field)

SKILLS

In VitroDrug DiscoveryBiotechnologySarBiochemistryBpfGmpDissolutionOrganic ChemistryDevelopment of Plga Based FormulationPharmaceutical IndustryValidationPeptidesAnalytical ChemistryScienceCharacterizationSecteur PharmaceutiqueChimie Analytique

ABOUT PATRICK GARROUSTE

MSc in Biochemistry and Ph.D. in Bioorganic Chemistry at the Université des Sciences et Techniques du Languedoc (USTL) in Montpellier, France (1995). During the thesis, I achieved the synthesis and the physical characterization of linear and cyclic pseudopeptidic inhibitors of the HIV protease.Post doctoral position at the Institute of Organic Chemistry, Lausanne, Switzerland, as a Post-doc (19••••98): synthesis and characterization of several TASP molecule using the “chemoselective” reaction of unprotected peptide.1998 to 2004 : Analytical Development Manager in the Pharmaceutical Development Department at Debio RP (Debio group, Martigny, Switzerland). 2004 to 2015 : Pharmaceutical Development Director in the same group.From 2015 : Drug Research and Development Director at DebiopharmSpécialisations : Development of in vitro dissolution test for sustained release formulation (from 1 to 6 month of release)validation of analytical methods according to GMP rulesPeptide chemistryDevelopement of SR PLGA based formulation (from 1 week to 6 months)Delivery of API BCSII (poor solubility)

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