Valbiotis is a Research & Development company dedicated to scientific innovation for preventing and combating metabolic and cardiovascular diseases.
To achieve this goal, Valbiotis has developed an exclusive and unique scientific approach founded on specific combinations of plant-based molecules. The active substances, which are called “totums”, act directly on the key metabolic parameters of the body. Our unique approach focuses on prevention by providing health nutrition solutions.
In a few words
Listed on Euronext Growth in 2017 4 patent families Prediabetes – Type 2 diabetes – Dyslipidemia – Arterial hypertension – MAFLD/NAFL/NASH 3 locations in France: Périgny (17), La Rochelle (17), Riom (63) 36 experts: 75% in R&D, 50% women
Our vision, our mission
The rising incidence of metabolic and cardiovascular diseases around the globe is a major public health challenge: prevention is key to ensure that the health of at-risk individuals does not deteriorate. For each of these diseases, there is a period during which they can still be treated for known risk factors. Poor outcomes are not inevitable. And this is not just our point of view; it is supported by science. The science we develop at Valbiotis.
Our Research & Development platform works tirelessly to develop our plant-based active substances (totums), while always ensuring that our processes meet the most demanding international standards at every phase. Our R&D efforts have been handsomely rewarded, as all our plant-based active substances are protected by international patents and intellectual property. At Valbiotis, R&D is in our DNA.
Our quality process
At Valbiotis, our R&D focuses on the multi-target complementary and/or synergistic effects of the various biomolecules from the plant totum. Our products are derived from food plants and plant extracts, and are subject to rigorous scientific and clinical development.
Valbiotis’ teams have extensive scientific, clinical and regulatory expertise, and exceptional skills in: – New-generation screening techniques, – Complete characterization of plant substances, – Plant biomolecule extraction, purification, fractionation and pharmacomodulation processes, – Preclinical studies in multiple areas: molecular, cellular, tissue, in vivo.
To improve our expertise and accelerate innovation and development, Valbiotis: – Entered into partnerships with leading academic centers as soon as the company was founded, – In September 2018, Valbiotis created its own 1,200 m² platform for Discovery and Preclinical Research on metabolic diseases at its site in Riom, France.
The Quality Assurance Department at Valbiotis is responsible for ensuring its Quality Management System, certified ISO 9001, meets the highest standards.
Our Quality Management System, a reflection of our commitment, allows us to: – Ensure the quality, traceability and integrity of our R&D data, – Conduct clinical trials compliant with the highest standards and Good Clinical Practices, – Ensure the safety and quality of our products from the earliest stages of development and throughout their life cycle, – Guarantee the materials sourced are of the highest quality and perfectly traceable, – Control manufacturing processes in accordance with applicable standards (HACCP, Good Manufacturing Practice for Manufacturers of Food Supplements), – Control the quality of the services provided by our subcontractors and suppliers, – Meet the expectations of our stakeholders.
ISO 9001 certification was granted in March 2021 for the “design, development and production of solutions aimed at the prevention and fight against metabolic and cardiovascular diseases”. Download the ISO 9001 certificate here
Compliance, quality, integrity, and anticipating the expectations of our stakeholders are the cornerstone of our Quality Policy, thereby ensuring the highest level of quality is achieved at each stage of the life cycle of our products, from preclinical research to clinical development, and ultimately industrial-scale production.
Launch of the PHASE II HEART study for TOTUM•070. ISO 9001 certification granted.
A global strategic partnership with Nestlé Health Science signed. Launch of the Phase II/III REVERSE-IT study for TOTUM•63. Three new active substances in the pipeline: TOTUM•070, TOTUM•854 and TOTUM•448.
Successful industrial-scale production of TOTUM•63 in collaboration with the Pierre Fabre group. Positive results from the Phase II clinical study of TOTUM•63.
Creation of a proprietary technical platform for Discovery and Preclinical Research on our Riom site.
Initial public offering on the Euronext Growth market. TOTUM•63: Presentation of Phase I/II clinical results at the American Diabetes Association 77th Scientific Sessions in San Diego, California.
Discovery of the “TOTUM•63” active substance.
The company is founded in La Rochelle.
After completing a thesis on nutrition in the field of cardiovascular and metabolic diseases at the Laboratory of Applied and Fundamental Bioenergetics (U1055 INSERM) at Joseph Fourier University (Grenoble, France) under the supervision of Professor Xavier Leverve, Sébastien worked at a spin-off of the Free University of Brussels in Belgium on a drug candidate in the area of enteral and parenteral nutrition. In 2007, he joined the Lescuyer Laboratory, where he was rapidly entrusted with management of the Research & Development Department. In this position, he notably oversaw the entire application process for one of the only health claims ever to obtain a positive response from the EFSA for reducing a risk factor for cardiovascular diseases. Sébastien chaired the Biopôle Santé – Réseau Expert, Territoire d’Innovation, Service de Valorisation en Santé (regional expert network for innovation and optimization in the health sector) for the Poitou-Charentes region and later for Nouvelle-Aquitaine for over five years until March 2017. He was also granted the French higher degree authorizing the supervision of research (HDR – Habilitation à Diriger des Recherches) from Blaise Pascal University (which later became the University of Clermont Auvergne, Clermont-Ferrand), allowing him to officially supervise PhD students. Sébastien is an active member of the French Nutrition Society and the American Diabetes Association. He has written over 35 international scientific articles and papers, and has developed more than five patent families.
Jocelyn has an MBA from Panthéon Sorbonne University, a financial analysis degree from HEC Paris, and is a graduate of Paris IAE. For close to 20 years, Jocelyn worked in various project management roles in executive positions within SMEs. He has brought several structural and cross-disciplinary operational projects to successful completion, providing support during the creation, restructuring and development of businesses, notably in the agro-food sector. For close to 10 years, he worked as Administrative, Logistics and General Services Manager for the Lescuyer Laboratory, and participated in the global development and structuring of the company. He also managed multi-disciplinary teams (sales administration, logistics, accounting, HR) comprising approximately 20 employees. Jocelyn provides Valbiotis with strategic, financial and organizational expertise as well as extensive knowledge of the healthcare market and healthcare products in particular. He manages the finance, management control, human resources and general services departments.
Pascal was a Lecturer at the University of Clermont Auvergne between 2008 and 2018, and has headed the institution’s technical functional assessment platform since 2010. He has also launched several international scientific partnerships with Vanderbilt University (Nashville, USA), the Maine Medical Center Research Institute (Portland, USA) and the University of Texas (Houston, USA) with regard to research projects on the pathophysiology of type 2 diabetes. In 2005, Pascal graduated with a PhD in Biological and Biochemical Health Sciences from Montpellier University and was also granted the French higher degree authorizing the supervision of research (HDR – Habilitation à Diriger des Recherches) in 2016. Pascal has been heavily involved in Valbiotis since it was founded in 2014. As a member of the Scientific Committee, Pascal was in charge of collaborative projects involving the University of Clermont Auvergne and Valbiotis. In 2017, he was appointed Chief Scientific Officer (CSO) at Valbiotis and took over management of the Discovery and Preclinical and Translational Research Department. As such, Pascal is also at the helm of our two R&D centers in La Rochelle and Riom. Furthermore, he is the co-inventor of a number of key technologies used for the development of Valbiotis.
After managing a team responsible for the implementation and development of clinical study management at Nantes University Hospital, in 2002, Murielle founded BIOFORTIS, a leading CRO (contract research organization). In addition to achieving the growth of her company, Murielle contributed to local economic development by attracting the MÉRIEUX pharmaceutical group to Nantes. In 2009, BIOFORTIS joined the MÉRIEUX group, and Murielle successfully managed its integration into the MÉRIEUX NUTRISCIENCES subsidiary. In addition, Murielle took on the role of Chair of the “Atlanpole Biothérapies” cluster from 2012 to 2018 with a view to establishing new therapies and accelerating the development of personalized medicine by facilitating joint university and industry research programs.
Laurent has a PhD in Physics and Chemistry, with a specialization in nanomaterials, from the Pierre and Marie Curie University and the CEA (French Commission for Atomic Energy), and a Master of Advanced Studies in Condensed Matter Physics from UPVI-ESPCI (Paris). He has acquired extensive experience in the science and techniques associated with nanomedicine, a field in which he has worked for over a decade. His research is at the forefront of chemistry, biology and physics, and has enabled him to design a certain number of practical applications in nanomedicine, such as the NanoXray technology, which could herald the start of a new era in cancer treatment. Before founding Nanobiotix in 2003, for several years, Laurent worked as a consultant in the development of nanotechnology applications for groups such as Sanofi (pharma), Guerbet (medical imaging) and Rhodia (chemistry), as well as for biotech start-ups. The author of 35 international scientific publications and papers, Laurent has filed many patents and topped off his career with a post-doctorate at the Institute for Lasers, Photonics and Biophotonics of SUNY (State University of New York), Buffalo, in the United States.
Sébastien is an expert in the field of Consumer Healthcare and Nutrition and, over the past 20 years, has held various positions in marketing and innovation for leading pharmaceutical groups. He has gained unique experience in consumer marketing and product innovation on a national and global scale. Sébastien previously worked as Managing Director at Biofortis Europe, a subsidiary of Mérieux Nutrisciences; Director of Global Innovation “Probiotic Platform” at Merck Consumer Healthcare; Director of Global Strategic Marketing at Merck Consumer Healthcare; Global Marketing Manager at Reckitt Benckiser; Europe Marketing Manager and Marketing Manager at Boots Healthcare International, and Marketing Manager at Sanofi Aventis.
Jean Zetlaoui has over 30 years’ experience in various international executive positions and cutting-edge expertise in the pharmaceutical and nutrition sectors, their environments and their challenges. The Scientific Director of NOVARTIS Pharma SAS, and then Special Scientific Adviser to the CEO and a member of the Executive Committee, Jean was also Chief Medical Officer and a member of the Executive Committee of Nestlé Health Science in Vevey, Switzerland, for two years, contributing to the growth of the personalized medicine and health nutrition business segments. For close to 20 years, Jean also held various executive and R&D positions at SANOFI, including that of Vice-President and Head of Market Access, Vice-President and Head of Global Regulatory Affairs, and Vice-President and Deputy Head of Global Medical Affairs. Jean is also Vice-President of ARIIS (alliance for research and innovation in health industries) and Chairman of the working group on the attractiveness of France for clinical research headed by Leem, an association of French pharmaceutical companies. Before joining the pharmaceutical industry, Dr. Zetlaoui was a hospital practitioner at the Bicêtre University Hospital (CHU). Jean has a PhD in Medicine and is specialized in anesthesia and resuscitation. He also completed an Executive MBA in Finance and International Business at the ESSEC Business School (1991).
A graduate of ICN Business School in Nancy, with a post-graduate degree in accounting (DECS), and a member of the French Society of Financial Analysts (SFAF), Agnès began her career in 1986 at the Banque de Vizille, specialized in mid-cap transactions, which merged in 2011 with other entities of the Crédit Mutuel Alliance Fédérale group to create CM-CIC INVESTISSEMENT. From 1990 to 1997, she served as Financial Director and Board Member of the SHB hotel group in Lyon, which went on to merge with ACCOR. In 1997, she joined AVENIR TELECOM, a distributor specialized in mobile telephony, for whom she led the initial public offering on Eurolist C in November 1998. For 17 years, as the Administrative and Financial Director of the group (1,800 employees and €290 million in revenue in 2015), she managed a number of mergers and acquisitions and also oversaw investor relations. In 2015, she was appointed Financial Director of the transport and logistics group TRANSALLIANCE (3,000 employees and €600 million in revenue), which operates in seven European countries. From June 2016 to February 2018, she was the Administrative and Financial Director at IDEOL, an innovative company created in 2010 in La Ciotat (46 employees, €4 million in revenue) and a leader in floating offshore wind power.