
Jim Smeeding is a co-founder and executive leader at Indication BioScience, bringing more than four decades of experience across pharmacy practice, health economics, specialty pharmacy, and pharmaceutical company formation.
Mr. Smeeding is a founder of the Center for Pharmacoeconomic Studies at the University of Texas College of Pharmacy and has been a long-standing leader in applied pharmacoeconomics, outcomes research, and managed care systems integration. He previously served as Executive Director of the National Association of Specialty Pharmacy (NASP), where he played a central role in shaping the specialty pharmacy industry, before leaving to focus on company building and discovery efforts at Indication BioScience.
Over the course of his career, Mr. Smeeding has held leadership roles spanning hospital pharmacy, clinical services design, home infusion therapy, managed care services, disease management, and specialty pharmacy. He is an experienced pharmaceutical executive who has developed and led multiple companies from initial funding through successful exits.
Mr. Smeeding is a founder and former president of the International Society for Pharmacoeconomics and Outcomes Research (ISPOR), a past president of the Texas Society of Hospital Pharmacists, and an inventor on patents related to digital technologies in prescription adjudication. He has authored more than 50 publications on health value assessment and outcomes-based healthcare and holds degrees in pharmacy from the University at Buffalo and an MBA from the University of Texas.
Mathew Sherwood is Chief Executive Officer and co-founder of Indication BioScience, where he leads the development of ATO-875 (Atorvo+), an oral fixed-dose combination program advancing toward Phase 2 clinical development in cardiovascular disease.
Mr. Sherwood brings over two decades of experience across healthcare, life sciences, and pharmaceutical development, with a focus on translating differentiated formulation science into clinically and commercially viable drug programs. He has overseen product development activities spanning formulation, preclinical strategy, CMC, regulatory planning, and clinical execution, including the successful completion of a Phase 1 clinical program.
Previously, Mr. Sherwood served as Vice President of Product Development at an early-stage pharmaceutical company and has held officer and director roles at a publicly traded life sciences company. Earlier in his career, he worked as a consultant in specialty pharmacy and healthcare services, contributing to the establishment of the National Association of Specialty Pharmacy, where he served as an Industry Liaison.
Mr. Sherwood is an inventor on multiple issued patents related to pharmaceutical formulation and combination strategies and works closely with an experienced clinical, regulatory, and scientific advisory team to advance capital-efficient development programs.

Harry Koppel serves as Chief Financial Officer of Indication BioScience, where he leads financial strategy, capital planning, and operational finance in support of the company’s clinical development and partnering objectives.
Mr. Koppel brings extensive experience from global financial institutions, including senior roles at Barclays in London, where he was responsible for capital structure analysis, financial planning, and execution of complex financial strategies. His background spans corporate finance, capital markets, and strategic financial management across growth-oriented and regulated environments.
At Indication BioScience, Mr. Koppel oversees financial governance, budgeting, forecasting, and investor relations support as the company advances its lead program toward Phase 2 clinical development. He works closely with the executive and clinical teams to align financial strategy with development timelines, regulatory planning, and business development initiatives.
Mr. Koppel is known for his disciplined approach to financial management and his ability to support capital-efficient execution in complex, high-stakes operating environments.

Mr. Pechenik is a registered patent attorney with over a decade of experience obtaining, defending, and challenging some of the country’s most valuable and highest profile patents. Mr. Pechenik has represented numerous Fortune 500 companies on their patent matters, across the agricultural, chemical, pharmaceutical, biotech, and technology industries. His clients have included Pfizer, Roche, Sanofi- Aventis, Wyeth, DuPont, Pioneer Hi-Bred, Motorola, and Google. After working in the patent departments of the international law firms Kaye Scholer in New York and Quinn Emanuel in San Francisco, Mr. Pechenik founded Calyx Law. There, Mr. Pechenik works closely with businesses to design and implement their patent strategy. Mr. Pechenik graduated from New York University School of Law, and holds a Bachelors of Science from the University of California, San Diego, with majors in Biochemistry and Cell Biology, and Cognitive Neuroscience.

30 + years in pharma for clinical development and medical affairs for global drug development and cardiovascular product launches.
Initially served as Associate Medical Affairs Director at Merck International for Mevacor launch, the first lipid lowering drug of its class. Medical Consultant to Pfizer cardiovascular development team for cardiovascular endpoint committee liaison services in the phase 3 study of Lipitor. Senior Medical Director at Esperion Therapeutics for the development of bempanoic acid FDA approved as the first in class lipid lowering drug with a unique safety profile to avoid skeletal muscle adverse side effects. Previously academic appointment as the Medical Director at the Harvard Clinical Research Institute for cardiovascular drug and device development.
Member of the American Medical Association and former member of the Royal Society of Medicine UK since 1988
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Gary Conte brings over 30 years of experience in the pharmaceutical industry to his role as Vice President of Pharma at Indication BioScience. With expertise in commercial product development, sales, marketing, business development, and operations, Gary has played a key role in the growth and success of multiple start-up pharmaceutical companies.
Prior to joining Indication BioScience, Gary held senior leadership positions at multiple specialty pharmacies and healthcare organizations, where he spearheaded payer contracting, business development, and revenue development initiatives. He also served as Vice President of Business Development at HealthPlan Data Solutions, focusing on innovative software solutions for payers and specialty pharmacies.

Dr. Luis A. Rojas has more than thirty-five years of experience in clinical development, biostatistics, and regulatory strategy across the pharmaceutical and medical device industries. He has led global biometrics and clinical teams from early-phase research through pivotal studies and regulatory submissions, with expertise spanning neurology, rare and metabolic diseases, oncology, immunology, infectious diseases, gastroenterology, and cardiovascular medicine.
As Chief Executive Officer and President of InCSD, LLC, Dr. Rojas provides strategic and scientific leadership in adaptive and master protocol design, regulatory-grade modeling and simulation, and inspection-ready study planning. He previously served as Chief Clinical Development Officer for the Curyx Bio Platform and held senior leadership roles at IQVIA, Parexel, and Clinipace–Target Health.
A recognized thought leader in innovative trial design and advanced biometrics, Dr. Rojas has delivered invited presentations at global scientific and regulatory conferences, including the DIA Annual Meeting and the World Orphan Drug Congress. His recent work integrates physiologically based pharmacokinetic modeling with regulatory frameworks to accelerate drug development for rare and pediatric diseases.
Dr. Rojas holds a PhD in Statistics from Rafael Belloso Chacín University and is an active member of the DIA Adaptive Design Scientific Working Group, the American Statistical Association, and Sigma Xi.

Dr. Cutlip completed his cardiology fellowship at Beth Israel Hospital in 1997. He is currently Chief Medical Officer at Baim Institute (formerly Harvard Clinical Research Institute). He has over 25 years experience in the design and management of randomized clinical trials and has directed efforts for event adjudication and medical safety reviews. He has been a leader in Data and Safety Monitoring Board activities and has chaired several of these committees. He is a co-founder of the Academic Research Consortium, which has developed endpoint definitions and standardization of event adjudication methods in clinical trials of coronary stenting, transcatheter cardiac valves and other technologies. He has published over 300 papers related to clinical outcomes and clinical trial results in interventional cardiology.

Dr. Matt Cavender, MD, MPH, is an Associate Professor at the University of North
Carolina in Chapel Hill, NC. He is the Therapeutic Director of Cardiovascular Disease
for the UNC Clinical Research Alliance and the Director of Cardiovascular Clinical
Trials. Dr. Cavender earned his medical degree from the University of Alabama School
of Medicine and a Master’s in Public Health from the Harvard School of Public Health.
He completed his internship and residency in Internal Medicine at Duke University, a
clinical fellowship in cardiology at the Cleveland Clinic, and an interventional cardiology
fellowship at Brigham and Women’s Hospital. His primary research focuses on clinical
trials and observational comparative effectiveness research to evaluate strategies for
preventing cardiovascular events in high-risk patients, including those with coronary
artery disease, diabetes, and obesity. Dr. Cavender is an Associate Editor for Circulation:
Cardiovascular Interventions, serves on the board of the National Cardiovascular Data
Registries, and co-chairs the American College of Cardiology’s working group on public
reporting of clinical outcomes. He has authored over 100 book chapters and scientific
manuscripts in journals such as The New England Journal of Medicine, Lancet, JAMA,
JACC, and Circulation. In addition to his research, he is clinically active, specializing in
catheter-based therapies for patients with advanced coronary artery disease, peripheral
vascular disease, and valvular heart disease.

Professor Saoirse Elizabeth O’Sullivan (@ScienceSaoirse) received her doctorate from Trinity College Dublin in 2001 and moved to the University of Nottingham in 2002 as a Research fellow where she began researching cannabinoid pharmacology. She was made Lecturer in 2007, Associate Professor in 2011 and Full Professor in 2019. She has nearly 60 peer-reviewed articles and 3 books chapters on cannabinoid pharmacology. Her academic interests were on the therapeutic potential of cannabinoid-based therapies in cardiovascular disease, diabetes, cancer and inflammatory bowel disease. Her research methodologies spanned from cellular and animal models, to human healthy volunteer studies, systematic reviews and early phase clinical trials. Saoirse left academic in 2019 and is now the Vice President of Translational Sciences at Artelo Biosciences (Home - Artelo Biosciences), running the preclinical research strategy of multiple pipelines including a peripheral restricted CB1 agonist (being trialled in cachexia), a cannabidiol cocrystal (for use in anxiety/depression), and a fatty acid binding protein (FABP) inhibitor platform (lead molecule is being investigated in neuropathy). She also runs an independent consulting company called CanPharmaConsulting Ltd, acting as scientific advisor to pharmaceutical and biotech companies.

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