Projects leaders can apply at any time. If interested, candidates (academics or startups) apply to the programme by submitting an application form. According to their specific needs, applicants may benefit from several steps of the programme.
Non-French European applicants can apply if they can prove that they have collaboration with French partners (academic team or company).
Preselection pitches :
Once the application file has been submitted to MATWIN, the project is pre-selected for a pitch presentation before a multidisciplinary jury meeting in November in Paris.
The projects selected by the experts will then be submitted to the MATWIN International Board members (on the basis of the application dossier), who will be the ones deciding which projects can be included in the programme.
The written comments of the MATWIN Board members will be sent to all applicants by end of January.
On the basis of experts assessments, projects are invited or not to continue the process (coaching) for a possible presentation at the MATWIN International Board meeting at the end of the process. Projects are not competing against each other, only intrinsic value and development potential are taken into account.
The pre-selection pitches will take place in Paris on November 19th 2019!
Composition of the pre-selection jury:
Composition of the pre-selection jury:
Composition of the pre-selection jury:
- Jean-Yves Bonnefoy(Syndivia);
- Gilles Avenard (Acticor Biotech);
- Jean-Marc Herbert (Go Capital);
- Jean-Pierre Armand (Gustave Roussy);
- Sergio Roman Roman (Institut Curie);
- Philippe Genne (Oncodesign);
- Sébastien Barradeau (Diagast);
- Stéphane Loze (Angels Santé );
- Benoit Barteau (BPI France);
- Jérôme Fournier Majoie (Fondation Fournier Majoie)
Coaching sessions :
Individual work sessions are frequently organized to optimize projects’ structuring and industrial orientation. Technology transfer offices are associated and included in the process. They are invited to participate to every working session organized by MATWIN next to the project leaders to benefit from the feedback.
Development Plan Review
Driven by innovation specialists and experts in preclinical and clinical development, this work session addresses the project’s background and allows to optimize its structure and industrial orientation. This session aims at supporting projects leaders in their valorization approach.
It takes place once a year in February/March in Paris.
Training for the Board meeting audition
This second work session aims at preparing the project leader for his interview by the MATWIN International Board strengthened by the 1st session contributions. Experts speakers bring their expertise to optimize the project presentation. This session is in a real condition format (in English, in front of a multidisciplinary jury) to reflect the MATWIN Board interview.
By end of the two coaching sessions, the coaches will select the 6 best projects that will be interviewed by the prestigious MATWIN Board.
It takes place once a year in April in Paris.
Jean-Marc HERBERT has more than 30 years of industrial experience in pharmaceutical R & D at international scientific and managerial positions.
Jean-Marc was Senior Vice President, Head of Discovery at Sanofi. Jean-Marc has been instrumental in the discovery and development of more than 70 drug candidates including marketed products such as Plavix® and Arixtra®. He holds an engineering degree in Biochemical Engineering and a PhD in Cellular and Molecular Biology from the University of Clermont-Ferrand. He did his Ph.D. in Cell Biology and Biochemistry at the Clinical Research Center in London (UK).
Today Jean-Marc is President of ARKELY-Consulting, a consulting company in translational research for the discovery and development of innovative medicines.
Dr. Avenard is Board member or adviser for several companies and Chief Executive Officer of G1J-IDF, a seed venture fund in Life Sciences. From 1997 to 2010, he served as Chief Operating Officer of BioAlliance Pharma SA (BIO – NYSE-EURONEXT) since he co-founded the company. From 1990 to 1997, Dr. Avenard served as Medical Director of Development in the Cassenne Laboratories division of Hoechst Marion Roussel (Sanofi-Aventis Pharma).From 1976 to 1990, Dr. Avenard held various positions with the National Blood Transfusion Center in Paris, including Medical Director of Bio-Transfusion (LFB), providing human plasma products. He has also served as a physician in hemobiology and blood transfusion at the Blood Center of Pitié-Salpétrière Hospital in Paris. Dr. Avenard received his MD as well as degrees in hematology and hemobiology & blood transfusion from the School of Medicine at the University of Paris V. He is currently member of the Biotech Working Group at LEEM (pharmaceutical French trade association). He is also expert for Research Tax Credit at the Ministry of Research.
Jean-Yves Bonnefoy is CEO of Anagenesis Biotechnologies since January 2014. He is also President of the Life Sciences Competitiveness Cluster, Alsace BioValley, Board member of biotech companies Anagenesis and SILABE and of the engineer school ESBS. He is a member of the scientific advisory board of iTeos Therapeutics and Centre de Recherche des Cordeliers. He is also member of the investment committee of the TTO, SATT Conectus. Before Anagenesis Biotechnologies he co-founded Transgene Spin-off, ElsaLys Biotech. He was for 8 years VP, R&D of Transgene SA. From 2002 to 2005, he launched and managed the Canceropole Lyon Rhône-Alpes. From 1992 to 2002, he headed the Centre d’immunologie Pierre Fabre. From 1998 to 2002, he was Director of the Immunology Department of the Glaxo-Wellcome Institute in Switzerland. From 1985 to 1987, he was scientist at the Research Centre of Schering-Plough in France. He is author and co-author of more than 200 publications and reviews (H-index 55-30-13). Jean-Yves holds a PhD in Immunology, a “Thèse 3ème cycle” in Biochemistry and followed the Senior Management Program of the London Business School, in the UK.
Dr. Herrera has more than 25 years of experience in the pharmaceutical industry with a strong focus in oncology drug development and marketing. Before setting up his own oncology consultancy – Alain Oncologie Consulting (AOC) -, he headed the global Oncology business at Sanofi for ten years, where he was Vice President for the Global Oncology Business Strategy and Development (2007-2008) and Head of the Global Oncology Franchise (1998-2007). He contributed to the worldwide registration of Oxaliplatin (Eloxatin®) and Rasburicase (Fasturtec®/Elitek®), as well as the Gastric and Head & Neck indications for Docetaxel (Taxotere®). His previous responsibilities within the pharmaceutical industry included the roles of Chairman and CEO of Chiron Therapeutics Europe, Managing Director at Pierre Fabre Oncology Laboratories and Head of the Oncology Platform at Roger Bellon (Rhône Poulenc). In addition to these roles, since 1991, Dr. Herrera has been a Hematologist Consultant at Antoine Beclere Hospital.
Grégoire Prévost is a Doctor in Cellular and Molecular Biology. He now has more than 30 years of experience in drug discovery in oncology and early phases of clinical development. Dr. Grégoire Prévost is the founder, owner and CEO of CIPREVO, an expertise provider company supporting innovation projects in the fight against cancer. CIPREVO is based in France and its main clients are Pharmas, CROs, Biotechnologies, Start-ups, Consortiums, Investors, Funds, University groups or patient associations. His expertise is recognized by the French government with the approval of the Research Tax Credit and the Empowerment to Direct Research (HDR). In addition, Grégoire Prévost is also the co-founder of the Sino-French School of Oncology in Wuhan (China). Previously, Grégoire Prévost was successively researcher at IOCMH (France), Director of Scientific Affairs at Ipsen-Beaufour and Chief Development Officer at Interna Technologies (Netherlands). He is the author of more than 65 international publications and 36 patent applications.
Dr. Thérèse Croughs has more than 20 years of experience in clinical development and regulatory affairs. She has worked in companies of varying sizes and clinical stages of development in the pharmaceutical and biotech industries in Europe, North America and Asia.
Thérèse Croughs began her career in the pharmaceutical industry at Bayer, where she worked on protocol definition and the conduct of several clinical trials, as well as the registration of several products, including r-FVIII in hemophilia. A. After 10 years at Bayer, Thérèse joined the Novo Nordisk team as International Medical Advisor for the clinical development in Europe of r-FVIIa for the treatment of severe bleeds. Thérèse Croughs continued her career at BioAlliance Pharma, where she held the position of Director of the Adhesive Technology and New Business Unit and Director of European Regulatory Affairs. More recently and for more than 6 years, Thérèse Croughs was the Medical Director of Cytheris where she was in charge of regulatory strategy and international development of the IL-7 immunotherapy program (r-hIL-7, a factor growth of the immune system). Thérèse Croughs is a graduate of the Faculty of Medicine of the Catholic University of Louvain – Brussels, Belgium. Since 2015, she is Chef Medical Officer for NEOVACS.
MATWIN Board interview :
Selected applicants submit their projects in front of the MATWIN International Board. This unique in Europe committee auditions the projects and labels those with the highest industrial development transfer potential. This committee’s feedback represents a significant added value for the project development.
After presenting to the Board, candidates may initiate discussions with certain members, or any other actor of the ecosystem (Biotechs, investors …) likely to collaborate on the development of the project. Auditioned projects will be monitored by the Board.