Dr. Saeho Chong brings more than 25 years of senior management experience, including more than a decade of strategic development in the pharmaceutical industry. He most recently served as Vice President, Early Development at Alnylam Pharmaceuticals, where he had a significant track record of success in R&D.
Previously, he served in roles of increasing responsibility and leadership at Bristol-Myers Squibb and Millennium (Takeda Oncology). He also held a prior position in the U.S. Food and Drug Administration’s (FDA) Office of Clinical Pharmacology and was a professor of Pharmaceutical Sciences, College of Pharmacy at Seoul National University.
Dr. Chong received his B.S. and Ph.D. in Pharmaceutics at the esteemed School of Pharmacy of the State University of New York at Buffalo. He received post-graduate training under the guidance of Dr. HL Fung at SUNY Buffalo and is currently an Adjunct Associate Professor of Pharmaceutical Sciences at SUNY Buffalo. He has held editorial board positions of the American Association of Pharmaceutical Scientists Journal, Drug Metabolism and Pharmacokinetics, Archives of Pharmacal Research, and the Journal of Pharmaceutical Investigation, and has authored more than 90 publications in peer-reviewed journals.
Saeho is a die-hard Buffalo Bills fan and is still working toward his first Hole-In-One.
Dr. Seong H. Jang brings a deep expertise in clinical pharmacology, having held considerable positions of increasing responsibility at FDA for nearly 20 years. His experience includes leadership roles in the Division of Infectious Disease Pharmacology, Office of Clinical Pharmacology, Center for Drug Evaluation and Research. He and his team contributed to the approval of an impressive portfolio of new drug products in multiple therapeutic areas, including transplant, special pathogen and anti-infectives.
He is widely recognized both internally and externally for his expertise and collaboration. Further, his contributions include serving as a cross disciplinary team leader in several NDA reviews and as an acting deputy division director for the Office of Study Integrity and Surveillance.
Dr. Jang earned his Ph.D. in biopharmaceutics from the College of Pharmacy at Ohio State University with focus in pharmacokinetics and pharmacodynamics and subsequently as a research fellow. He received his bachelor’s and master’s degrees from the College of Pharmacy at Seoul National University and has published numerous peer-reviewed articles and has often presented at scientific organizations such as the Clinical Trials Transformation Initiative, National Health Institutes, and the American Society for Microbiology.
Seong enjoys running in his free time. He even coordinated an “Elevar Runner’s Club” for an all-staff event.
Wade Smith is responsible for Elevar’s capital acquisition and deployment, accounting/controlling, financial planning and analysis, business development and portfolio optimization, marketing, market access, commercial operations and pricing functions in addition to serving as the corporate secretary.
With more than 30 years of experience as a financial and commercial executive, Wade Smith joined Elevar Therapeutics in January 2022 after spending the previous decade at Viatris (formerly Mylan Pharmaceuticals), a global health care company working in a broad range of therapeutic areas. Most recently, Mr. Smith was Viatris’ head of U.S. institutional commercial/finance from 2017-2022, functioning as the COO and CFO for the $1 billion+ division.
He developed a go-to-market strategy for more than 100 new products, overseeing launch pricing, customer contracting, managed care engagement, demand planning, and sales targeting in addition to portfolio selection and budgeting/forecasting. He previously held finance leadership positions of increasing responsibility in the energy industry, at Taggart Global USA, LLC and Nova Chemicals where his work included investor relations, mergers & acquisitions, initial public offerings (S-1), consolidations, and financial planning & analysis.
Wade started his career in public accounting and still holds an active CPA license in the Commonwealth of Pennsylvania. He earned a bachelor’s degree in business administration and accounting from Penn West – California University of Pennsylvania.
He enjoys trail running, hiking, and spending time with his wife and daughter.
Dr. Chris Galloway is an executive physician with more than 20 years of comprehensive medical practice and biotechnology experience. He joined Elevar in 2023 bringing extensive industry expertise spanning leadership roles in early and late-stage clinical development, medical affairs and business development in oncology and other therapeutic areas. His broad experiences include managing several successful Investigational New Drug Applications (IND), NDA, and BLA submissions to the FDA. In his role at Elevar, he oversees the global Clinical Development, Clinical Operations and Medical Affairs functions.
Most recently, he served as Chief Medical Officer at Diffusion Pharmaceutics where he led all pre-clinical and clinical development, medical affairs, drug safety, pharmacovigilance, medical monitoring and biometrics. Prior industry experience includes leadership roles in medical affairs and clinical development at La Jolla Pharmaceutical, Rakuten Medical, Merck and DaVita Clinical Research. Prior to his professional transition to clinical research, he worked for a decade as an emergency room physician.
Dr. Galloway received a B.S. in Biology from The University of Texas Austin and an M.D. from The University of Texas Medical Branch.
Chris is a Texan at heart, but loves raising his family in the beautiful and rugged outdoors of Colorado.
Mr. Jin joined the Board in 2020. He is the Co-Chief Executive Officer of HLB, Elevar’s parent company, and leads HLB Group as Chairman, bringing seasoned leadership and keen insights gained from a broad management background. He is committed to alleviating human disease and suffering by finding new treatments for patients with cancer and other illnesses throughout the world.
Mr. Nam has worked for more than 30 years at major Korean conglomerates, managing a wide range of areas including finance, sales and administration. He is currently the Co-Chief Executive Officer of HLB Life Science, an affiliate of the HLB Group, and serves as Vice Chairman of the HLB Group.
Mr. Baek is an expert in finance and accounting, with over 30 years of experience overseeing these areas at major Korean conglomerates. He has served as the Chief Financial Officer of HLB and is currently the Co-Chief Executive Officer of HLB.
Mr. Dong Gun Kim joined the Board in 2020. He currently serves as Chief Executive Officer of Immunomic Therapeutics and previously as Chief Strategy Officer of Elevar and Chief Executive Officer of HLB. Prior to joining Elevar/HLB, Mr. Kim spent more than 30 years as a specialist in M&A, corporate finance and investment management at leading corporations and professional firms (law, investment banking and private equity) both in the U.S. and Korea. Mr. Kim has an A.B. in Physics from Harvard College and a J.D. from Harvard Law School.
Dr. Han joined the Board in April 2022. He is the Co-Chief Executive Officer of HLB Life Science and leads all new drug development activities. Yong-Hae has played major roles in multiple R&D organizations in the United States and Korea.
Dr. Chong was appointed to the role of Chief Executive Officer in March 2022 and is a member of the Executive Team. Saeho brings more than 25 years of senior management experience, including more than a decade of strategic development in the pharmaceutical industry.
Dr. Richard Kim is a Service Chief of Medical Gastrointestinal Oncology and Senior Member in the Gastrointestinal Oncology Department at Moffitt Cancer Center. He is a Professor of Oncology at the University of South Florida College of Medicine. Before coming to Moffitt in 2010, Dr. Kim was an associate physician in gastrointestinal malignancies at the Cleveland Clinic Taussig Cancer Center and a clinical assistant professor at the Cleveland Clinic Lerner College of Medicine of Case Western Reserve University.
Dr. Kim’s clinical and research interests focus on gastrointestinal tumors, in particular hepatobiliary and colon cancer. He is a principal investigator in multiple investigator-initiated and pharmaceutical phase I, II, III trials using immunotherapy and novel targeted agents.
Daneng Li, M.D. is an Associate Professor in the Department of Medical Oncology & Therapeutics Research at City of Hope, specializing in treating gastrointestinal cancers. Dr. Li currently leads the liver tumors program and is also the co-director of the Neuroendocrine Tumor Program at City of Hope. Dr. Li’s clinical and academic research is focused on the multidisciplinary approach to treatment of patients with neuroendocrine tumors (NETs). He leads several clinical trials focused on improving outcomes for patients with NETs and works closely with scientists in the development of the next generation of novel therapeutics.
Rachna T. Shroff, MD, MS, FASCO, serves as associate director of Clinical Investigations and co-leader of the Gastrointestinal Clinical Research Team at the University of Arizona Cancer Center (UACC) and is a professor in the Department of Medicine, chief of the Division of Hematology and Oncology, medical director for the Oncology Service Line and associate dean for Clinical and Translational Research for the University of Arizona College of Medicine – Tucson. Dr. Shroff joined UACC from MD Anderson Cancer Center in Houston. She is a clinical and translational investigator focused on developing novel therapies for pancreatic and hepatobiliary cancers and has led numerous clinical trials focusing on pancreaticobiliary tumors. She was the national principal investigator for SWOG 1815, which investigated a triplet chemotherapy regimen as a potential new standard of care for biliary cancers.
Mitesh J. Borad, M.D., is the Getz Family Research Professor and leads the Novel Therapeutics and Modalities Program at Mayo Clinic. Dr. Borad is an internationally recognized expert for treating patients with cholangiocarcinoma and has been extensively involved in developing novel cancer therapeutic platforms that leverage genomic medicine and gene/virus therapies, with a focus on tumors of the liver, bile ducts and pancreas. He has led the clinical development of novel anti-cancer agents in more than 50 first-in-human studies, including a multi-institutional team with collaborators at Mayo Clinic and the Translational Genomics Research Institute, which led to the discovery of fibroblast growth factor 2 (FGFR2) fusions in patients with intrahepatic cholangiocarcinoma, with the first demonstration of anti-tumor activity with FGFR inhibitors in this patient population. Subsequent work led to the FDA approval of three FGFR inhibitor cancer therapies.