Management team
Firat Yazicioglu
Firat joined GSK Bioelectronics in 2015, before Galvani’s formation in 2016. In his role as CPTO at Galvani, Firat leads the integrated product development efforts as well as the Translational and Engineering team, including the company’s platform engineering, neural interface engineering, surgical tools and development, translational science, product management, field clinical engineering and regulatory functions.
Prior to his role in Galvani, he spent 13 years at imec, Europe’s largest independent research centre in microelectronics and nanoelectronics. He developed devices and technologies for medical-grade wearable and implantable biomedical devices, including wireless cardiac monitoring patches, wearable EEG monitoring headsets and implantable neural probes for high density neural recording that got licensed to Global medtech companies or commercialised by imec. Firat was also involved in the creation of a San Francisco-based wearable healthcare start-up, Bloom Technologies.
With a Ph.D. in microelectronics from KU Leuven in Belgium, Firat has authored more than 100 peer-reviewed publications along with 20 patents, including a book on low-power biomedical microsystems. He has served on the technical program committees of European Solid State Circuits Conf (ESSCIRC), International Solid State Circuits Conf (ISSCC), and Biomedical Circuits and Systems Conf (BioCAS) and was Associate Editor for IEEE Trans. of Biomedical Circuits and Systems.
Kristoffer Famm
Kris is President and CEO of Galvani Bioelectronics, with the overall responsibility for the company’s path to and delivery of bioelectronic medicines to patients. He has built and led the company since its formation in 2016. Before his appointment to lead Galvani, he was founding VP and head of Bioelectronics R&D at GSK, which he launched in 2013. There he managed the unit’s extensive research towards establishing the treatment potential, disease reach and technology requirements for bioelectronic medicines. As such, Kris has set strategy and led delivery in the field from early vision and research through to the clinical-stage therapy platform company Galvani is today.
During his time at GSK prior to Bioelectronics R&D, Kris led the Protein Degradation Discovery Performance Unit, which was the first unit in industry to successfully pursue protein degradation as a therapeutic modality.He also headed up the GSK R&D Strategy Group 2009-2011.
Before joining GSK in 2009, he was a biopharma R&D-focused Engagement Manager at McKinsey & Company in London. Kris obtained his PhD in Molecular Biology at University of Cambridge under the supervision of Nobel Laureate Sir Greg Winter, following an MSc in Chemical Engineering at Lund University, Sweden.
Raolat Abdulai
Raolat Abdulai, M.D. is the Chief Medical Officer at Galvani. In her role, she is leading Galvani’s clinical organisation encompassing the clinical development, surgical, clinical operations, medical affairs, biostatistics, and disease biology-focused pre-clinical functions as well as the portfolio of current and future clinical studies. She joined Galvani from Sanofi, where she most recently served as the Global Clinical Lead for dupilumab in Immunology and Inflammation. She played a pivotal role in shaping the clinical strategies for multiple indication expansions across disease areas, most recently with the approval of the first ever biologic for chronic obstructive pulmonary disease (COPD), focusing on late-stage data to transform treatment paradigms and enhance patient outcomes.
Raolat is a pulmonary and critical care physician with an extensive background in early and late clinical development, digital biomarkers, and technology in clinical operations. Raolat received a B.S. in from the University of Maryland and an M.D. from Howard University. She completed her Internal Medicine training at the Mayo Clinic and her fellowship in Pulmonary and Critical Medicine at Harvard Medical School/Brigham and Women’s Hospital. She was also a fellow in the NIH-funded training program and completed her Masters in Medical Science in Biomedical Informatics at Harvard Medical School.
Sarah Mateen
Sarah is the Head of Legal and Chief of Staff at Galvani. In her role as Head of Legal, Sarah oversees and manages Galvani’s legal affairs and has primary accountability for company contracting needs, together with intellectual property and corporate risk management. As Chief of Staff, she supports the President & CEO and other members of the Management Team and leads on activities relating to the Galvani Board of Directors, company-wide internal engagement and management against company performance objectives.
Sarah has an MA in Law from the University of Cambridge. She trained and qualified at Slaughter and May in London, where she advised GSK on a number of deals including the formation of the Galvani Bioelectronics joint venture, upon completion of which she joined Galvani in early 2017.
Suzanne Bryant
Suzanne is Head of Finance at Galvani and joined the team in January 2019. In this role, Suzanne has accountability for all aspects of financial leadership including Galvani’s dynamic resource and spend management, financial reporting to the Board and shareholders, statutory reporting, cashflow management and long-term financial planning and forecasting. Suzanne and her team provide finance partnering across Galvani’s programmes.
Suzanne has over 20 years experience within GSK during which time she has held a number of different positions across the organisation including in Corporate Finance, Commercial Finance Partner, UK Pharma and Financial Controller, Norway Pharma based in Oslo. Prior to Galvani, Suzanne was Finance Director, Respiratory R&D providing financial leadership to the early stage Discovery Performance Units (DPUs).
Suzanne has a BSc in Mathematics from the University of Exeter. Prior to joining GSK she trained as a Chartered Accountant at KPMG in London.
Board of directors
Anurag Mehta
Anurag Mehta is the Head of Corporate Development at Verily where he is responsible for driving the inorganic growth agenda through acquisitions and investments to support strategic growth.
Before joining Verily, Anurag spent seven years across various roles at Johnson & Johnson in New York, including Global Head of Strategic Transactions for the Consumer Health Division, Venture Investor at JJDC (J&J’s venture investment fund), and Head of JLABS NYC (J&J’s startup accelerator in NY). Prior to J&J, he spent close to a decade in the Mergers & Acquisitions Group within the Investment Banking Division at Credit Suisse in New York. Anurag started his career in Product Development at Oracle Corporation in their Advanced Supply Chain Planning Division in Redwood Shores, California.
Anurag holds an MBA from the University of Chicago Booth School of Business, an MS in Industrial Engineering & Operations Research from the University of Florida, and a B.Tech. in Mechanical Engineering from the Indian Institute of Technology, New Delhi.
Ken Gabriel
Kaigham J. (Ken) Gabriel is currently the inaugural CEO of BioForge, a University of Pittsburgh organization with a mission to accelerate innovations and breakthroughs in the development and manufacturing of new biologic, precision medicines to speed their delivery, use and impact.
Before taking on this role, he served as the founding Chief Operating Officer of Wellcome Leap, a non-profit spin-out of the Wellcome Trust with a mission to accelerate human health discovery and innovation by building bold and unconventional programmes and funding them at scale. Prior to that, Ken was president and CEO of Draper, a spin-off engineering company of the Massachusetts Institute of Technology notably famed for developing the Apollo guidance computer in the 1960s. Ken’s roles prior to Draper include corporate vice president and founding colead of the Advanced Technology and Projects (ATAP) group at Google and deputy director and acting director of the Defense Advanced Research Projects Agency (DARPA) in the U.S. Department of Defense. Ken also was a tenured professor in both the Department of Electrical and Computer Engineering and the Robotics Institute at Carnegie Mellon University.
Ken earned his ScD in electrical engineering from the Massachusetts Institute of Technology. Recognized as a World Economic Forum Technology Pioneer, Ken has more than 200 technical publications and presentations and holds 14 patents ranging from signal processing to MEMS and materials.
Subesh Williams
Subesh Williams is Senior Vice President, Global Corporate Development at GSK, a role he was appointed to in September 2013. In his current role, Subesh is responsible for M&A and Business Development across GSK’s commercial businesses and has been involved in executing a number of transactions, including the creation of ViiV Healthcare (a HIV JV with Pfizer and Shionogi) and the three – way deal with Novartis which involved the acquisition of Novartis’ vaccines business, the creation of a JV in Consumer Healthcare and the sale of GSK’s oncology business. From 2009- 2013, Subesh was Chief Financial Officer of ViiV Healthcare, with responsibility for Finance, Business Development, IT and Supply. Subesh joined GSK in 1994 and has had roles of increasing responsibility in Finance and Corporate Development. Subesh is a chartered accountant and, prior to joining GSK, was a manager at PwC.
Galvani Bioelectronics Team
Andrew Williamson
Acting as the primary interface between Galvani’s Business and IT Operations organisations, Andrew leverages his expertise to ensure Galvani’s business systems are fit for purpose and running smoothly. Through solution architecting, vendor selection and assessment, implementation and ongoing technical engineering and support, Andrew maintains a detailed understanding of the IT platforms supporting business processes and ensures they are optimally deployed.
Daniel Chew
Daniel is a founding member of Galvani Bioelectronics and leads the Translational Research team within. The team is based in the UK with dedicated onsite electrophysiology laboratories, as well as managing academic and CRO collaborators externally.
Translational research for Galvani focuses on preclinical-to-clinical studies of autonomic nervous system neuromodulation, and the ability to modulate organ physiology and treat disease across an indication pipeline. Research explores the fundamentals of nerve physiology, translational biology, and pathophysiology, while discovering and optimising ways of interaction with disparate visceral neuroanatomy. This involves the pursuit of in silico, ex vivo, and in vivo electrophysiology methods to determine the efficacy and safety profiles of Galvani therapies, with the goal of delivering clinical therapy.
Prior to industry research at GSK and Galvani, Daniel studied Neuroscience at the University of London; Queen Mary (PhD – 2009), and the University of Cambridge (Post Doctorate – 2009-2013). Research from his academic career focused on understanding the dynamics of the peripheral nervous system, developing pre-clinical in vivo neurosurgical models, and novel neuroprosthetic design and application. Daniel is the Home Office License Holder and Risk and Ethics owner for in vivo research in Galvani, and is author to over 50 scientific publications and patent applications.
David Sokal
David works within the Translational & Engineering group to direct and perform in-house and collaborative electrophysiological studies in small and large animal models and human tissue, aimed at developing and refining clinically-relevant stimulation parameters. He also manages academic collaborations to elucidate biological mechanism of action in human tissues. David has a long-standing interest in neural interfacing; during his PhD he worked to develop high-density neuronal recordings with applications for the treatment of epilepsy. Prior to Galvani Bioelectronics, David has over 20 years of experience in Neuroscience, the last 15 of which has been in Psychiatric Drug Discovery within major international pharmaceutical companies.
Eric Irwin
Eric is board certified General and Vascular surgery with over 25 years of clinical experience in these areas. He is an adjunct professor of surgery at the University of Minnesota where he is involved in training for medical students, residents and practicing clinicians and is involved in clinical research activities.
During the past 18 years he has also worked with biomedical device companies developing therapies to treat cardiovascular and pulmonary diseases. In these efforts he has worked in initial proof of concept studies; with R&D teams to develop initial implantable systems and to improve their usability; and with Clinical and Regulatory staff in clinical protocol development and establishing clinical events committees for clinical trials.
Eric worked with Galvani Bioelectronics since its inception working to study the anatomy at proposed interface sites, develop surgical techniques for humans and perform risk assessments and risk mitigation strategies for the surgical procedures developed to implant the neuromodulation systems.
Grace Anderson-Barker
Grace is an Principal Scientist within the Clinical Development group at Galvani Bioelectronics. Her role centres around the design, execution and interpretation of high-dimensional flow cytometry experiments to support Galvani’s Indication Expansion Programme in the identification of novel disease targets for neuromodulatory therapy. Data from this work will provide comprehensive information about the immune phenotype of relevant disease models and identify biomarkers for monitoring disease progression and efficacy of neuromodulation. In parallel, training in clinical development and clinical operations is being undertaken to provide support for Galvani’s clinical work.
Isha Gupta
Isha is the Director of Product Management and Clinical Strategy at Galvani, where she has been with the company since early 2017. Over the years, she has held multiple roles across product development and translational sciences, helping advance the product from preclinical research to clinical application. In her current role, she leads clinical strategic development, supports regulatory, manages the field clinical engineering team responsible for product deployment at clinical sites and with patients, and oversees end-to-end product management.
Isha holds a PhD in Electronics and Electrical Engineering from the University of Southampton (2018), where her research focused on developing miniaturized devices for neural signal processing, with broader applications in Internet-of-Things (IoT) computing. Her scientific contributions are documented in over 50 peer-reviewed publications and patents. While at Galvani, she recently earned an MBA from Imperial Business School and contributed to global commercial strategy at ViiV Healthcare.
Jerry Hunsberger
Jerry is an in vitro/ex vivo Investigator within Disease Biology primarily supporting the respiratory portfolio projects. He has a keen interest in novel mechanisms and interfaces to achieve fiber selective modulation of peripheral nerves to treat disease. In this role, Jerry also works closely with the Target Discovery and Neuronal Modulation Devices groups to help identify user requirements and functionality testing of neuronal interfaces.
Prior to joining Galvani Bioelectronics, Jerry worked for 10+ years in GSK’s Respiratory Therapeutic Area Unit and Neuronal Targets Discovery Performance Unit supporting lead optimisation of various chemical series targeting GPCRs and ion channels, including INCRUSE ELLIPTA® (umeclidinium) and Dinirixin. His past work has predominantly utilised functional ex vivo tissue preparations, electrophysiology, and calcium imaging techniques.
Jerry holds a BSc in Biomedical Engineering from Drexel University.
Kristen Rall
Kristen leads the Business Development activities and Alliance Management. Leveraging her extensive experience and CA-AM certification, Kristen’s maintaining cultivates and manages crucial relationships with external partners ensuring best practice and synergies across Galvani to deliver value through partnerships.
Prior to joining the Galvani team, Kristen was with GSK for over 25 years in various roles including Finance, Commercial and Worldwide Business Development. Kristen holds an MBA from Temple University, and a B.S. in Finance from Drexel University.
Margriet Vervoordeldonk
Margriet is Director Immunoinflamation in the Clinical Development team. As such she is mainly focusing on the development of neuromodulation strategies for the treatment of (chronic) inflammatory diseases. Her main tasks are to participate in the design and execution of the clinical development strategy and is responsible for the execution of Galvani’s first clinical study. She lead’s and participates in the data review and analysis of the trial results in close collaboration with the Clinical Operations team. She provides expert scientific input to clinical trial documents and the program regulatory dossier and lead or assist with Competent Authority and Ethics Committee/IRB submissions together with the Regulatory team. In addition, she supervises R&D involving ex- and in vivo research delivering proof-of-concept studies on the target nerve performed in collaborative research projects with several universities in Europe.
Margriet holds a PhD in Biochemistry which she obtained at the university in Utrecht (The Netherlands). Previously she was working as COO at Arthrogen (Amsterdam, The Netherlands), a small biotech company developing gene therapy for arthritis. Holding also a position as University Teacher at the division of Clinical Immunology & Rheumatology (Academic Medical Centre (AMC)/University of Amsterdam) she was supervising the research-lines focusing on neuro-inflammationn and gene therapy in rheumatoid arthritis. Currently she holds a position as University Teacher at the Tytgat Institute (AMC) and contributes to the development of neuromodulation for the treatment of inflammatory bowel disease. She is author of over 60 peer-reviewed publications.
Phil Milliken
Phil is Director within Clinical Development group and head of Indication Expansion. He is responsible for overseeing programs to diversify our lead therapy into new therapeutic areas, to confirm proof of concept and translational path to clinic. This includes developing translational biomarker strategies to define mechanisms of action and therapeutic response in our clinical trials. Prior to this he was Disease Biology manager, leading multiple projects with our academic collaborators, to demonstrate effects of neuromodulation on defined neural circuits in differing disease conditions.
Phil has extensive non-clinical and clinical experience across multiple therapeutic areas. He joined GSK in 2007, working in Safety Pharmacology with an in vivo cardiovascular and translational focus, followed by a position in Safety Evaluation & Risk Management in the Global Clinical Safety & Pharmacovigilance group. He moved to Pfizer as Non-Clinical Drug Safety Lead for the Neuroscience & Pain Research Unit, before joining Galvani Bioelectronics in 2016. Phil gained a PhD in Physiology & Pharmacology at the University of Strathclyde, followed by a post-doctoral position at the University of Edinburgh in the Centre for Cardiovascular Sciences.