More info about Nacer Lounis

On-campus

Company
Janssen Pharmaceutica

Function
Senior Principal Scientist

More info about Tine de Marez

On-campus

Company
Johnson & Johnson

Function
Senior Director, Compound Development Team Leader TB

More info about Erik Niks

On-campus

Company
Leiden University Medical Center

Function
Neurologist - Pediatric neurologist

More info about Piet Hinoul

On-campus

Company
J&J Ethicon

Function
Global Head, Pre-Clinical, Clinical and Medical Affairs

Piet joined J&J in 2008, after 15 years of clinical practice, as the medical director for Ethicon Women’s Health and Urology for EMEA. Since then he has successfully contributed to the product development, evidence generation and commercial launches of dozens of devices across all the Ethicon platforms. Piet earned his MD degree from the University of Leuven and his PhD in Biomedical Sciences from the University of Amsterdam. He is a European Board-certified Gynecologist having trained in the UK and Belgium. He was division chief of urogynecology at the teaching hospital of Genk, Belgium. Piet served as President of the Flemish Society of Obstetricians and Gynecologists in 2007 and 2008. He published extensively on various topics of pelvic floor surgery, and has lectured internationally on them.

More info about Ad Sitsen

On-campus

Company
ClinPharMed Consultancy for Drug Development

Function
Owner

Prof. Dr J.M. Ad Sitsen completed his pharmaceutical studies at the State University of Utrecht in The Netherlands in March 1970 and obtained a Ph.D. in medicinal chemistry two years later. After having fulfilled his compulsory military service with the Royal Dutch Navy he began his medical studies in 1974, which he completed in 1980. He then specialized in pharmacology at the Rudolf Magnus Institute of the Medical Faculty of the University of Utrecht and subsequently trained for two years in internal medicine at the Academic Hospital of the same Medical Faculty. In 1984 he joined N.V. Organon, a business unit of Akzo Nobel, and has been involved in the clinical development of Remeron® from the beginning and also many other compounds. He retired in 2004 and now acts as a consultant to pharmaceutical companies. He was a member of the Dutch Health Council and a (part-time) professor of clinical pharmacology at the Medical Faculty of the Utrecht University, Utrecht, The Netherlands. He has published approximately 100 research articles and reports and was editor of volume 6 of the Handbook of Sexology: The Pharmacology and Endocrinology of Sexual Function (Amsterdam:Elsevier, 1988). He is co-editor of the Handbook of Anxiety and Depression: A biological Approach (New York: Marcel Dekker, 1994) and editor-in-chief of the major Dutch language textbook of pharmacology. Specialties: assessment of toxicological data, design of first time in man studies, clinical pharmacology, drug development, medical writing

More info about Paul Stoffels

Company
Johnson & Johnson

Function
Chief scientific officer

As Executive Vice President, Chief Scientific Officer, Johnson & Johnson, Paul Stoffels works with leaders across the organization to set the company-wide innovation agenda. He is a member of the Johnson & Johnson Executive Committee and chairs the Johnson & Johnson R&D Management Committee. Paul spearheads the Johnson & Johnson innovation pipeline by leading teams across the pharmaceutical, medical devices and consumer segments to discover and develop transformational healthcare solutions. He also steers Johnson & Johnson’s global public health strategy to make innovative medicines and technologies accessible in resource-poor settings. Paul’s visionary leadership was instrumental in the launch of Johnson & Johnson Innovation in 2013, which he now leads to fuel innovative science and technology through strategic partnerships, licensing and acquisitions. Paul also oversees JJDC, the oldest corporate venture fund in the life science industry. In addition, Paul has responsibility for safety of all products of the Johnson & Johnson Family of Companies worldwide. Previously, in his role as Worldwide Chairman, Pharmaceuticals, Paul was responsible for advancing the therapeutic pipeline of Janssen Pharmaceutical Companies of Johnson & Johnson. Under his leadership, Janssen rejuvenated its therapeutic pipeline, launching multiple new medicines and bringing years of life and quality of life to people all over the world. Prior to this, Paul held various R&D leadership roles within the pharmaceutical sector of Johnson & Johnson. He joined Johnson & Johnson in 2002 with the acquisition of Virco and Tibotec, where he was Chief Executive Officer of Virco and as Chairman of Tibotec, and led the development of a number of breakthrough products for the treatment of HIV. Paul studied Medicine at the University of Diepenbeek and the University of Antwerp in Belgium and Infectious Diseases and Tropical Medicine at the Institute of Tropical Medicine in Antwerp, Belgium. He began his career as a physician in Africa, focusing on HIV and tropical diseases research. Source website Johnson & Johnson

More info about Marcel Kenter

On-campus

Company
Paul Janssen Futurelab Leiden

Function
Director

Marcel Kenter studied molecular biology at Leiden University and obtained his PhD degree for his work on the genetics of the primate Major Histocompatibility Complex (Mhc) in the immunology department of Prof Johannes van Rood (Leiden University Medical Center (LUMC), the Netherlands). He continued his post-doctoral work on virology at the department of Prof. Ab Osterhaus (Erasmus Medical Center, the Netherlands) and on gene therapy at the Daniel den Hoed Cancer Center. In 1999, he became the first executive director of the Central Committee Involving Human Subjects (CCMO); the competent authority for clinical trials with medicinal products in the Netherlands. He has been director of Paul Janssen Futurelab Leiden since 2015.  

More info about Koen Andries

On-campus

Company
Janssen Pharmaceutica NV

Function
VP Scientific Fellow Infectious Diseases Discovery

Dr Koen Andries (1951) studied Veterinary Sciences and obtained his PhD at the University of Ghent, Belgium. He joined the team of Dr. Paul Janssen in 1982.  Using cell-based assays in search of antiviral compounds, his team discovered nanomolar inhibitors of uncoating of rhinoviruses, picomolar inhibitors of fusion of respiratory syncytial virus and several non-nucleoside reverse transcriptase inhibitors of HIV (TIBO’s, alpha-APA’s, and DAPY’s) with high activity against wild-type and resistant HIV-1 strains. Two of these became approved drugs: etravirine - intelence® and rilpivir - edurant®, and a third one is being developed as a microbicide in a vaginal ring to prevent HIV infection (dapivirine). Dr Andries also led the team that discovered R207910/TMC207 (bedaquiline – sirturo®), a first in-class new anti-tuberculosis drug, and its unique mechanism of action. Bedaquiline is the first molecule with specific activity against the ATP synthase, one of the most fundamental enzymes in biology, and the first antibiotic known to interfere with the generation of energy. He grandfathered bedaquiline from discovery to early development and eventually full development as the microbiology leader. He authors 173 papers, 179 abstracts and 32 patents, and is Professor emeritus at the University of Antwerp.

More info about Andreas Wallnöfer

On-campus

Company
BioMed Partners Venture Capital (former Head of Clinical Research & Exploratory Development at F. Hoffmann-La Roche Ltd.)

Function
General Partner

More info about Justin Hay

On-campus

Company
Medicines and Healthcare products Regulatory Agency

Function
Pharmacokinetics Assessor

Justin Hay (1980) completed his BSc (Biomedical Science) with majors in Pharmacology, Microbiology & Immunology (2001) and graduated with First Class Honours (2002). In 2007 he was conferred his PhD in Medicine (Pharmacology) from the University of Adelaide, Australia. His thesis investigated the pain sensitivity of chronic opioid users and explored novel pharmacological analgesic strategies for these patients. From March 2007, Justin was in the position of Senior Clinical Scientist at CHDR, where he investigated how biomarkers of the central nervous system could be used as a screening tool in early drug development, with a particular interest in analgesics and pain models. In 2011 he was awarded his Certificate in Human Pharmacology from the Faculty of Pharmaceutical Medicine of the Royal Colleges of Physicians of the United Kingdom and in 2014 was awarded the Graduate Certificate (with distinction) in Clinical Pharmacology from King's College London. In October 2015 he started as Pharmacokinetics Assessor for the MHRA and is a member of the EMA's Modelling and Simulation Working Group (MSWG).

More info about André Elferink

On-campus

Company
Dutch Medicines Evaluation Board

Function
Clinical epidemiologist

I am a physician with a neurological and methodological background (clinical epidemiologist). Since 1992  I work as a senior clinical assessor at the Dutch Medicines Evaluation Board. As a clinical assessor I advice the Dutch Medicines Evaluation Board and the European Committee for Proprietary Medicinal Products whether a medicinal agent may be approved for a claimed indication and if so, under which conditions. The MEB I started as a generalist but may main field of interest is neurology.  In this context  I am member of the CNS-Working party involved in setting up regulatory Scientific Guidelines. Within the neurology my special fields of interest are Multiple sclerosis, Parkinson's Disease and Epilepsy. As generalist I  became member of the Scientific Advice Working party in 2012.

More info about Rob Zuiker

On-campus

Company
CHDR

Function
Senior Clinical Scientist

Rob Zuiker (1968) studied medicine at the University of Amsterdam. He was employed as a physician at the Royal Dutch Navy until 2000. After obtaining a master degree in Business Administration at the Nyenrode University Breukelen, he worked as a medical advisor for Eli Lilly Netherlands. From 2007 Rob joined CHDR as a clinical research physician and has since been working on a wide range of projects. His main field of expertise is on biomarker development as a screening tool for early drug development in asthma and the central nervous system. He is registered as a clinical pharmacologist since 2012, and from 2013 onward he holds a position of senior clinical scientist in the central nervous system research group.

More info about Hans-Georg Eichler

Company
European Medicines Agency

Function
Senior Medical Officer

More info about Robert Klautz

On-campus

Company
Leiden University Medical Centre

Function
Thoracic Surgeon

Prof Klautz did his medical training at the University of Leiden Medical School. After medical school he spent two years as a research fellow at the Cardiovascular Research Institute of UC San Francisco from 1991-1993, after which he did his PhD in Leiden on Cardiac Mechanics, specifically in single ventricle hearts. He did his Surgical training at the Erasmus Medical Center in Rotterdam. In 2002 he returned to Leiden as a staff surgeon at the department of Cardiothoracic Surgery, where he became chair of the department in 2008. His main clinical and research interests are in mitral and aortic valve reconstruction, alternative surgical strategies in heart failure treatment, and ischemia-reperfusion injury. He is a Council Member of EACTS, and an active member in the “acquired cardiac disease domain” committee, member of the STS, the AATS and of several national organizations.

More info about Matthijs Moerland

On-campus

Company
CHDR

Function
Research Director Translational Biomarkers

Matthijs Moerland (1980) studied Biomedical Sciences at Leiden University. He was trained in vascular biology at the department of Cell Biology of Erasmus University Rotterdam (2002-2006, Prof F.G. Grosveld), where he obtained his PhD investigating lipoprotein metabolism and atherogenesis in humanized animal models. In 2007 he joined CHDR as senior clinical scientist in the Vascular Medicine research group, focusing on the integration of immunology, endocrinology and endovascular reactivity in translational medicine. From 2014 onwards, Matthijs Moerland is heading a separate research area, entitled Translational Biomarkers, which comprises the selection, qualification and implementation of non-routine biomarkers in drug development.

More info about Joris Rotmans, MD, PhD

Company
LUMC

Function
internist-nephrologist

Dr. Joris Rotmans is an internist-nephrologist and associate professor at the Department of Nephrology of the Leiden University Medical Center (LUMC) in the Netherlands. He received his PhD in 2005 at University of Amsterdam on new therapeutic strategies for vascular access for hemodialysis. In 2008-2009, he did postdoctoral research on vascular tissue engineering at the Australian Institute of Bioengineering and Nanotechnology in Brisbane, Australia. Since 2010, he combines clinical work as internist-nephrologist with vascular and renal research at the Department of Nephrology of the LUMC. His main focus of research is vascular access for hemodialysis. He was the principle investigator of the DialysisXS consortium in which a novel method to generate in vivo engineered blood vessels was developed. He received the first prize at the Investors forum of the Dutch LifeScience Conference in 2013. In 2014, he received a prestigious VIDI grant from NWO that allows him to expand his research group and to continue his research on vascular tissue engineering.

More info about Janneke Meulenberg

On-campus

Company
Arthrogen

Function
CEO

Janneke Meulenberg has over 25 years of experience in the Biopharmaceutical industry. She graduated cum laude from the University of Groningen, received a PhD in Biochemistry from the University of Amsterdam and holds an MBA from RSM Erasmus University. Janneke Meulenberg started her career in industry at ID-Lelystad, where she headed a world leading R&D team developing veterinary vaccines in collaboration with Boehringer Ingelheim. She joined the management team of Amsterdam Molecular Therapeutics (now UniQure) in 2000, where she was responsible for developing Glybera® from research to registration studies. Glybera® is the first gene therapy that has received market approval in the Western World. Between 2008 and 2015, Janneke Meulenberg was CEO of ORCA Therapeutics B.V., a biopharmaceutical company developing innovative oncolytic adenoviruses and sinds 2015 she is CEO of ViciniVax BV, a company developing immunotherapeutic cancer vaccines. In 2015, Janneke Meulenberg was appointed COO of gene therapy company Arthrogen BV. She is author of numerous peer-reviewed publications, book chapters, and inventor on several patents.

More info about Inge de Lepeleire

Company
MSD Europe

Function
Director Translational Pharmacology

More info about Koos Burggraaf

On-campus

Company
CHDR

Function
Research Director CVS & Metabolism

Koos (Jacobus) Burggraaf (1959) graduated in BioPharmaceutical Sciences (MSc) and Medicine (MSc) at Leiden University with a specialization in clinical pharmacology and qualified cum laude as an MD at Leiden University. Since 1990 he has held several positions at the Centre for Human Drug Research where he also obtained his PhD. He is professor ‘Translational Drug Development’ at the Leiden Academic Center for Drug Research. He is a board certified clinical pharmacologist and has held clinical attachments at several hospitals mainly in internal medicine since 1997. He is a full member of several (inter)national societies on clinical pharmacology and member of the board of the Dutch Association of Clinical Pharmacology. He is a member of the Leiden educational team for clinical pharmacologists and actively involved in the training of PhD students. He has published over 125 manuscripts in peer-reviewed journals. His main focus of interest has been on early drug development (phase I/II), with special emphasis on biologicals, including method development (in particular in cardiovascular medicine, endocrinology, endothelial function, immuno-inflammation, gastrointestinal function), and pediatric drug research.

More info about Johan Garssen

Company
Danone/Nutricia Research

Function
Director Immunology Platform

More info about Ingrid de Visser

On-campus

Company
CHDR

Function
Senior Clinical Scientist

Ingrid de Visser – Kamerling (1975) graduated in Medical Biology from Leiden University in 1998. She subsequently worked at the Centre for Human Drug Research as project leader and PhD student. She obtained a PhD degree from Leiden University (2003) and became registered clinical pharmacologist (2005). From 2004 – 2007 she worked as policy coordinator at the research department of the Netherlands Heart Foundation. In 2007 she returned at CHDR as interim manager of education until 2008. From 2008 onward she holds a position of senior clinical scientist in the field of immunology and cardiovascular research. She is also the secretary of CHDR’s Scientific Advisory Board.

More info about Rick Kuntz

Company
Medtronic

Function
Senior Vice President and Chief Scientific, Clinical and Regulatory Officer

More info about Geert Jan Groeneveld

On-campus

Company
CHDR

Function
Research Director CNS

Geert Jan Groeneveld was trained as a Neurologist at the University Medical Center Utrecht and performed his PhD on the subject: “New pharmacotherapeutic treatment strategies for Amyotrophic Lateral Sclerosis”. Before joining CHDR, Geert Jan worked on enzyme replacement therapy for Pompe Disease and on a gene therapy project for Parkinson's Disease at biotechnology company Genzyme. Since 2009 he is Research Director at the Centre for Human Drug Research (CHDR) in Leiden, and is responsible for research in the areas of neurology and pain. He is also a staff-member at the department of Neurology of VU University Medical Center, Amsterdam, where he performs clinical work as a neurologist. His primary scientific interest is in early phase drug development for the treatment of neurodegenerative diseases and neuropathic pain. He has published more than 35 scientific articles and is actively involved in the training of PhD students at CHDR.

More info about Oliver Bisazza

Company
Medtronic

Function
Director Regulatory Policy

More info about Saco de Visser

Company
Paul Janssen Futurelab Leiden

Function
Teacher and Clinical Pharmacologist

Saco de Visser became a registered clinical pharmacologist and obtained his PhD degree from Leiden University in 2003. After two years of business development at the Centre for Human Drug Research (CHDR) in the Netherlands, he worked at the Netherlands Organisation for Health Research and Development (ZonMw) setting up a subsidy programmes for Orphan and Expensive drug outcome research. In addition Saco was Director of Cluster Development at Leiden Bio Science Park and Medical Liaison for pipeline sourcing in North-West Europe at Nycomed (currently Takeda). Since 2016, he combines his position as Programme Officer for Public-private drug research collaboration at ZonMW with his position as Head of Education at Paul Janssen Futurelab Leiden.

More info about Adam Cohen

On-campus

Company
Centre for Human Drug Research

Function
CEO and clinical pharmacologist

Adam Cohen (1952) graduated in Pharmacy and Medicine from Leiden University. He subsequently joined the department of Clinical Pharmacology of the Wellcome Research Laboratories in Beckenham, UK where he obtained experience in early drug development. This work led to a PhD thesis about the development of an antihistamine (acrivastine) and an antiepileptic (lamotrigine). Further training in internal medicine was obtained at King’s College Hospital in London. Phase II-III drug development experience was obtained as European Clinical project leader for t-PA at Wellcome. Since 25 years, he is director of the Centre for Human Drug Research (CHDR). CHDR also play an increasingly prominent role providing consultancy to pharmaceutical industries, with special emphasis on early drug development. He is professor of Clinical Pharmacology at Leiden University and has a clinical attachment at the department of nephrology at Leiden University Medical Centre. He is author of more than two hundred publications about a wide range of clinical pharmacological subjects. He is executive editor of the British Journal of Clinical Pharmacology.

More info about Richard Shull

Company
Shell

Function
Head of Deal Structuring and Trading Fundamentals

More info about Pierre Peeters

Company
Organon

Function
Former site head early stage development

Pierre Peeters is Chief Operations Officer, responsible for all financial and operational activities within CHDR. In addition, Pierre is Research Director for food studies, as well as microdose studies. Pierre has more than 30 years experience in pharmaceutical industry, both at a CRO as well as, in medium/large Pharma (Organon, Merck /MSD) where he was responsible for the study design, conduct and reporting of several hundred early clinical trials and clinical development plans in various indications. Pierre received his degree in Chemistry at the University of Nijmegen and his PhD in Bio Pharmaceutics at Utrecht University. He is a registered Clinical Pharmacologist.