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1. Advancing ALS genetics through accessible testing
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2. Nociceptor-macrophage crosstalk in endometriosis: insights into pain and disease progression
- Dr. Michael S. Rogers
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3. Pioneering proteomics: insights on advancements in the science of proteins
- Prof. Ruedi Aebersold
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4. The state of the art in secondary pharmacology
- Dr. Jean-Pierre Valentin
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5. How liver X receptor regulates intestinal regeneration and tumor growth
- Dr. Srustidhar Das
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7. Using real-world insights on drug interactions to inform drug development
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8. The role of preregistration and registered reports in improving research transparency and reproducibility
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9. Decoding aging: how a proteomic clock predicts mortality and disease across populations
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10. Role of ETS2 in autoimmune and inflammatory diseases
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11. Restoring glucose metabolism: a new approach to reversing cognitive decline in AD
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12. The safety, toxicology, and regulation of antibody-drug conjugates
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13. MicroRNA as a biomarker for early detection of amyotrophic lateral sclerosis
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- Dr. Paul Alan Cox
- Dr. Rachael Dunlop
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15. Cancer vaccines
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16. The regulation of cell therapy
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17. How and why neurons die in Alzheimer's disease?
- Prof. Bart De Strooper
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18. The future of blood tests in cancer treatment
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19. Role of marketing authorization holder in drug safety
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20. Synthetic whole embryo models and their applications
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21. Scale-up challenges in the production of nanomedicines from lab to industry
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22. Artificial intelligence in precision medicine
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23. Translational medicine: the risk of failure in delay and how to reduce it
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24. Challenges and solutions of scaling up
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26. Management of generic drug development: challenges and opportunities
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27. MassBank development and future
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28. Elite controllers of HIV: from discovery to future therapies
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29. Translational research in amyotrophic lateral sclerosis (ALS)
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30. Rheumatic diseases and musculoskeletal pain
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31. Towards developing a universal influenza vaccine
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32. Predicting asthma exacerbations using machine learning models
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33. PANDAS: a potential link between group A streptococcal infections and neurological disorders
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35. Artificial intelligence in guiding cancer treatment decisions
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36. Characterizing barriers to care in migraine
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37. Monkeypox: etiopathogenesis, prevention, and treatments
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39. Kidney xenotransplantation
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40. CAR-T and TCR-T cellular immunotherapies in oncology
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41. MAPS: the business of medical affairs
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42. Hypertrophic cardiomyopathy: therapies and treatments
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43. Combating the HIV epidemic
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44. Epigenetic pharmaceuticals used in the clinic
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45. Precision cancer medicine: development and future
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46. Pediatric cancer testing
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47. Opposition to vaccination: a transatlantic discussion
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48. Elective caesarean sections from an evolutionary perspective
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49. Antiphospholipid syndrome and Lupus
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50. Prescribing medications to children - a GP’s view
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51. Antigen-specific immunotherapy for autoimmune diseases (ASIT)
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52. Recent key advancements on mechanotransduction in cardiovascular health
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Topics Covered
- What is secondary pharmacology and why is it important?
- The International Consortium for Innovation and Quality in Pharmaceutical Development
- Key insights from the DruSafe survey
- Insights on current practice in secondary pharmacology and the consortium’s recommendations
- Challenges and opportunities in the field
Biography
Dr. Jean-Pierre Valentin is a scientist with over 30 years of experience in the pharmaceutical industry, specializing in drug discovery, safety pharmacology, and investigative toxicology. He earned his Ph.D. in Physiology and Pharmacology from the University of Montpellier, France, followed by postdoctoral research at the University of California, San Francisco.
Dr. Valentin began his career at the Pierre Fabre Research Centre, contributing to the discovery and development of three drug candidates. He later joined AstraZeneca, where he established and led the Department of Safety Pharmacology, supporting the safety assessment of approximately 200 candidate drugs across multiple therapeutic areas. His work contributed to the development and registration of several marketed products.
In 2014, he joined UCB-Biopharma as Senior Director and Head of Investigative Toxicology, overseeing safety science across the company’s portfolio and modalities.
He is a former President of the Safety Pharmacology Society and serves as co-chair of both the HESI Proarrhythmia Subcommittee and the HESI Cardiac Steering Team. He is also a member of the Board of Trustees and Executive Committee of HESI, Chair of the IQ-DruSafe Secondary Pharmacology Working Group, and EFPIA representative on the ICH E14-S7B committee.
Dr. Valentin is actively involved in education and mentoring through scientific societies, universities, and industry associations. He has authored or co-authored several patents and over 250 peer-reviewed publications and book chapters.
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External Links
Talk Citation
Valentin, J. (2025, July 31). The state of the art in secondary pharmacology [Audio file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved August 14, 2025, from https://doi.org/10.69645/CELX5395.Export Citation (RIS)
Publication History
- Published on July 31, 2025
Financial Disclosures
- Dr. Jean-Pierre Valentin has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.