Colin Sandercock brings more than 30 years of experience advising life sciences companies on a broad range of legal matters, including domestic and international patent litigation, compliance, procurement, and licensing. Before joining Cue Biopharma, Sandercock was most recently a Partner at Perkins Coie since 2009. Prior to Perkins Coie, he held positions within legal firms including Proskauer Rose where he co-chaired the firm’s Life Science Practice Group; Heller Ehrman, where he co-chaired the firm’s Intellectual Property Practice Group; and Foley & Lardner, where he chaired the firm’s Chemical Practice Group. His technical experience includes life science, pharmaceutical compositions and biologics, organic and inorganic chemistries, as well as chemical and biochemical engineering. Sandercock has served as an adjunct professor of law at George Washington University Law School, lecturing on the licensing of intellectual property rights, and on the AAA Patent Advisory Committee for Patent Disputes. He received his J.D. from the Catholic University of America and received a M.S.E. in Engineering degree in Chemical and Biochemical Engineering from the University of Pennsylvania, and a B.S. in Chemistry and Mathematics from Moravian College.

Kerri-Ann Millar serves as the Chief Financial Officer.  Before joining Cue Biopharma, Ms. Millar served as Corporate Controller for Flexion Therapeutics, Inc., a biopharmaceutical company focused on the development of local therapies for the treatment of patients with osteoarthritis, where she developed the finance function for the newly public company to support the commercialization of its first approved drug. Prior to Flexion Therapeutics, she served as a Finance Specialist for Curis, Inc., a biotechnology company focused on the development of oncology treatments. Prior to Curis, Ms. Millar spent over 10 years in audit and finance functions at several investment banks in the Boston area and four years at PricewaterhouseCoopers. She earned a B.S. in Accounting and Finance from Boston University and is a Certified Public Accountant.

Dr. Baker has over 20 years of drug development experience in the pharmaceutical industry. From 2000 to 2019, he served as Vice President, Immunology R&D at Johnson & Johnson (Janssen/Centocor) where his responsibilities included clinical development of Remicade, Simponi and Stelara, as well as other major clinical drug programs. His supervision and oversight of numerous Phase I-III trials in multiple disease areas, led to more than 15 regulatory approvals in the US, Europe and Japan. In 2015, Dr. Baker assumed the role of Disease Area Stronghold Leader at Janssen where he was responsible for Phase II & III clinical development plans for rheumatology products and the overall portfolio strategy in rheumatology and immunology. Following his retirement from Janssen in 2019, Dr. Baker served as CEO and founder of Kira Therapeutics and more recently as Executive Director on the board of Galapagos Therapeutics from April 2022 until October 2024. Dr. Baker received his Medical Degree from the University of Pennsylvania and completed his Medical Residency at Hershey Medical Center and Fellowship in Rheumatology and Immunology at the University of Pennsylvania, followed by a Research Fellowship in Rheumatology at Mass General Hospital.

Matteo Levisetti brings extensive experience leading global clinical development for mid and large-size pharmaceutical companies. Prior to joining Cue Biopharma, Matteo served as Chief Medical Officer at DNAtrix directing and managing clinical operations and regulatory strategy for several clinical trials. Matteo also served as Chief Medical Officer at Dauntless Pharmaceuticals where he was responsible for all aspects of clinical development of endocrinology and oncology assets. Previously, Matteo directed immuno-oncology programs as Executive Director of Clinical Development at Mirati Therapeutics. Before joining Mirati, Matteo served as Global Head & Vice President, Translational Medicine, Immunology and Inflammation at Roche Pharma Research & Early Development and held several senior positions with Pfizer, including Global Clinical Lead. While working with Pfizer, Matteo led multiple early clinical development programs across several therapeutic areas, including endocrinology, immunology and oncology. Earlier in his career, Matteo held joint appointments as Assistant Professor in the Departments of Medicine, Pathology, and Immunology at Washington University School of Medicine. Matteo received his MD from the University of Chicago Pritzker School of Medicine, completed residency training in internal medicine at the University of Chicago Hospitals, and completed subspecialty training in endocrinology and a research fellowship in immunology with Dr. Emil R. Unanue at Washington University School of Medicine, St. Louis, Missouri.

Lucinda Warren has over 30 years of global experience in the pharmaceutical and biotechnology sectors. Most recently, she served as vice president of business development for Neuroscience and Japan Regionally at Johnson & Johnson from 2014 to 2024, where she was responsible for end-to-end business development, including licensing, mergers and acquisitions, and alliance management. Her leadership was instrumental in optimizing resources, fostering high-performing teams, and cultivating strong relationships with stakeholders. Lucinda’s extensive experience also includes significant roles at Janssen Cilag Australia and Centocor/Janssen Biologics, where she led business units and managed global transitions, consistently delivering value through strategic transactions. Lucinda holds a Bachelor of Science in Biological Sciences with a minor in Neurology from the University of Alberta and is an alumna of the Women in Bio Board Room Ready program. She currently serves on the boards of International School Services (ISS) and the Association of Strategic Alliance Professionals (ASAP), contributing her expertise in finance and governance.