New Frontiers in 3D | Visionaries Speak – Détails, épisodes et analyse

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New Frontiers in 3D | Visionaries Speak

InSphero

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Technologie

Fréquence : 1 épisode/79j. Total Éps: 4

Join us for a virtual fireside chat with visionaries in biopharma! We’re bringing together biopharma key option leaders recognized for their contributions to innovative human disease research and translational safety to share their thoughts on technologies that are transforming drug discovery.

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Données mises à jour le 14/07/2026

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Is Drug Screening in 3D Ready for Automation?

Épisode 4

lundi 4 octobre 2021 • Durée 58:31

Our Panelists

Dr. Terry Riss, Senior Product Manager, Cell Health, Promega Corporation

Dr. Terry Riss started the Cell Biology program at Promega Corporation in 1990. He managed the development of cell viability, cytotoxicity, apoptosis, and protease assay systems and lead efforts to identify and promote multiplexing of cell-based assays to determine the mechanism of cell death. He now serves as Senior Product Manager, Cell Health, involved in outreach educational training activities, including validating assay systems applied to 3D cell culture models. Terry is also an editor of the In Vitro Cell-Based Assays section of the Assay Guidance Manual hosted by The National Center for Advancing Translational Sciences (NCATS) at the NIH.

Dr. Tim Spicer, Senior Scientific Director, Department of Molecular Medicine, Scripps Research

Dr. Tim Spicer is the Senior Scientific Director in the Department of Molecular Medicine at Scripps Research. He has more than 30 years of experience in drug discovery, including ten years at Bristol-Myers Squibb. He is currently the director of HTS and discovery biology and co-directs the screening center at Scripps. Tim supervises HTS assay development & related efforts, including technology development funded through the NIH with an award for the “Advanced Development and Validation of 3-Dimensional Spheroid Culture of Primary Cancer Cells using Nano3D Technology”. He has authored >125 drug-discovery-related publications and is an inventor on 3 patents.

Dr. Jan Lichtenberg, Co-Founder & CEO, InSphero

Dr. Jan Lichtenberg is Co-Founder and CEO of InSphero – the largest biotech specialized in 3D cell-culture technologies for discovery and safety. Jan co-founded InSphero in 2009 and grew the company to 65 employees in Switzerland and the US while expanding the business to encompass all top 15 global pharmaceutical companies. Prior to InSphero, Jan had VP R&D and Product Management positions at Hocoma AG (medical robotics) and Uwatec (microelectronics). He holds a Ph.D. from the University of Neuchâtel and managed a research group at the Swiss Federal Institute of Technology (ETH), Zurich. Since 2021, he is a Board Member of the Society of Laboratory Science and Screening (SLAS).

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T1D: Emerging Perspectives on Disease Pathogenesis, Prevention and Treatment

Épisode 3

lundi 3 mai 2021 • Durée 58:16

Our Panelists

Prof. Matthias Hebrok, Professor at the Diabetes Center at the University of California San Francisco

Matthias Hebrok is Hurlbut-Johnson Distinguished Professor in Diabetes Research at the Diabetes Center at the University of California San Francisco. He received his Diploma degree in Cell Biology from the Albert-Ludwigs University, performed his PhD thesis at the Max-Planck-Institute, and conducted his postdoctoral research at HHMI at Harvard University. His laboratory has made seminal contributions to our understanding of how embryonic signals control the fetal development of the pancreas and its insulin-producing beta cells. His recent work has implemented the information gained from these studies to generate functional beta cells from human stem cell populations for cell therapy purposes.

Prof. Matthias von Herrath, Vice President and Senior Medical Officer at Novo Nordisk

Matthias von Herrath holds a dual appointment as Vice President and Senior Medical Officer at Novo Nordisk and Professor at the La Jolla Institute for Immunology Center for Autoimmunity and Inflammation. He received his medical degree from the Freiburg Medical School in Germany and completed his residency work in the Internal Medicine/Immunology department at the Freiburg Medical Center. For his postdoctoral work, Dr. von Herrath went to The Scripps Research Institute and worked in its Neuropharmacology and Immunology departments. Matthias is committed to clinical translation of immune-based interventions in autoimmune and metabolic diseases. His expertise and main strength is working at the interface of experimental research to interpret and refine early phase I/II clinical trials in order to optimize strategies for phase 3 trials and drug approval.

Prof. Mark Peakman, Senior Director of Autoimmunity and Type 1 Diabetes research at Sanofi

Mark Peakman trained in medicine at University College London and pursued postgraduate training in clinical immunology. After his PhD on the immune system in type 1 diabetes he held a senior clinical research fellowship at the University of Pittsburgh. He returned to the UK to oversee research at King’s College London in the Department of Immunobiology, focused on T lymphocytes in autoimmune disease. In 2019 Mark took a position as Senior Director of Autoimmunity and Type 1 Diabetes research at Sanofi, with the goal of designing and implementing strategies to bring disease modifying therapies to patients with autoimmunity.

Does Physiological Complexity Kill Scalability?

Épisode 2

vendredi 23 avril 2021 • Durée 01:08:44

Our PanelistsAcademic Perspective

Prof. Jaap den Toonder, Professor and Chair of the Microsystems section, Eindhoven University of Technology

Jaap is a full professor and Chair of the Microsystems section at Eindhoven University of Technology, and former Principal Scientist and Chief Technologist at Philips Research. He received his PhD in Mechanical Engineering from Delft University of Technology. His research focuses on the investigation and development of novel microsystems design approaches and out-of-cleanroom fabrication technologies. His application focus is on microfluidic chips, biomedical microdevices, organs-on-chips, and soft microrobotics. The section’s research approaches are often biologically inspired, translating principles from nature into technological innovations.

Academic Perspective

Dr. Peter Loskill, Assistant Professor, Research Institute for Women’s Health, Eberhard Karls University Tübingen

Peter is an Assistant Professor at the Research Institute for Women’s Health Faculty of Medicine at Eberhard Karls University Tübingen. He is also Head of Innovation Field at Fraunhofer IGB, Coordinator of the European Organ-on-Chip training network MSCA-ITN-EUROoC, and Vice-Chair of the European-Organ-on-Chip-Society (EUROoCS). He holds a PhD in Physics from Saarland University and worked as a postdoctoral fellow at UC Berkeley. In 2015, he was named as one of Technology Review’s “Innovators under 35 Germany” and awarded a Fraunhofer ATTRACT starting grant. His interdisciplinary µOrganoLab combines approaches from engineering, biology, physics and medicine to generate and apply novel microphysiological tissue models recapitulating complex human biology in vitro.

Industry Perspective

Dr. Florian Fuchs, Senior Principle Scientist, Nuvisan Innovation Campus Berlin

Florian is a Lab head within Lead Discovery at the Nuvisan Innovation Campus Berlin and former group leader on complex cellular models and cell-based screening at Novartis Basel. He holds a PhD in Chemistry from the Ludwig Maximilians University at Munich.

Biopharma Perspective

Animal-Free Drug Safety Testing: Challenges and Opportunities

Épisode 1

mercredi 10 février 2021 • Durée 01:05:29

This episode aired originally live at https://newfrontiersin3d.com/

In this podcast we address key questions, such as:

Do animals predict human drug safety correctly? What are the general limitations?
How can we increase predictivity of drug safety for patients?
What are the challenges for evaluating new therapeutic modalities?
What are the most promising new animal-free technologies and testing strategies for risk assessment?
What will drug safety risk assessment look like in 2030?

Our Speakers

Pharmaceutical Industry Perspective

Dr. Stefan Platz, Senior Vice President and Head of Clinical Pharmacology and Safety Services, R&D, AstraZeneca

Stefan is a senior R&D leader and passionate scientist at AstraZeneca globally leading clinical pharmacology, pharmacometrics, as well as toxicology and pathology. Creating ground-breaking medicines and being led by innovative science is in the center of his work. Stefan is a board-certified toxicologist in addition to earlier qualifying as a certified veterinary pathologist at the University of Munich. He has over 25 years of experience working across global pharmaceutical companies including Roche and AstraZeneca.

Academic Perspective

Prof. Thomas Hartung, Professor, Johns Hopkins University Bloomberg School of Public Health

Thomas is a Professor of Evidence-based Toxicology and Director of the Center for Alternatives to Animal Testing at Johns Hopkins University Bloomberg School of Public Health, and Professor of Pharmacology and Toxicology at the University of Konstanz. He is a passionate advocate for replacing animal testing with more ethical and predictive in vitro models and is investigating new applications for big data and artificial intelligence in toxicity testing.

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New Frontiers in 3D | Visionaries Speak – Détails, épisodes et analyse

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