Dr. Blain is an internationally known expert in cell cycle and cancer biology, and is one of the world’s experts on p27Kip1. She has been studying cell cycle regulation for more than 25 years as an NIH funded investigator and tenured Associate Professor at the SUNY Downstate Medical Center. She founded Concarlo, capitalizing on discoveries she made and patented. She was trained at Princeton, Columbia and the Memorial Sloan-Kettering Cancer Center.

Arthur Klausner is an experienced life science venture capitalist and company executive. He earned his M.B.A. from the Stanford University Graduate School of Business and his B.A. in Biology from Princeton University. He was previously CEO and a board member of Goldilocks Therapeutics, Gem Pharmaceuticals, and Jade Therapeutics. He earlier spent a total of 18 years as a life sciences venture capitalist at Domain Associates and Pappas Ventures. He currently serves on the Board of Directors of Monopar Therapeutics (Nasdaq: MNPR), and on the Life Sciences Investment Review Board for the New York University Innovation Venture Fund.

Dr. Allamneni is a biopharma R&D expert with almost 20+ IND/IMPD submissions, 6 NDA/MAA approvals, and a track record of efficiently developing therapeutic candidates of various modalities. Forward-thinking leader in R&D strategy and tactical planning, and a highly regarded operational manager for key R&D functions. Impactful global regulatory interactions with FDA, MHRA, BfArM, ANSM, PMDA, Health Canada, TGA etc. during clinical development, partnership, and commercialization. Formerly with Turning Point, Jazz Pharmaceuticals and Genentech.

Mr. Mraz’s career has been focused in the financial markets for over 30 years since he joined JPMorgan in 1989. In 1999 he was a co-founding partner of the money management firm, Ospraie Management, where he is still an active partner today.In 2015 he teamed with Dr. Stacy Blain to found Concarlo and guides the team on all financial mattersIn 2017, he lead the development of the Ospraie AgScience team and platform, which currently invests in catalytic agricultural biotechnology.

Natalia specializes in liposome and lipid nanoparticle drug delivery systems. Prior to her current role, she held various positions at Evonik Vancouver laboratories, facilitating transition of customer projects through various stages of development, from proposal scoping to formulation development to early clinical manufacturing. Natalia has over 20 years of experience in lipid nanoparticle drug delivery field and has been involved in all aspects of liposome manufacturing, starting from early-stage formulation design, process development, scale-up and early clinical manufacturing. Prior to Evonik, she worked at a number of Vancouver based drug delivery companies (CDRD/adMare, Celator/Jazz, Inex), focusing on liposomal products. Natalia holds undergraduate degree in Chemistry from University of British Columbia.

Dr. Grace Chen received her Ph.D. in immunology at the University of Toronto, Canada. Following that, Grace completed two postdoctoral fellowships, published extensively, and have led numerous research projects. She has over 15 years of experience in the fields of cell biology, immunology, and hematology. Prior to her current role, she served as a research scientist at Concarlo where she spearheaded the optimization and preclinical development of Concarlo’s lead compound.

Dr. Kate Coleman is a cell and molecular biologist with research background in cell cycle control and mechanisms regulating genome integrity. She received her PhD at the University of North Carolina at Chapel Hill under the direction of Dr. Jean Cook, where she studied the cell cycle transition from G1/S phase and its regulation by the E3 ubiquitin ligase CRL4Cdt2. She later joined the lab of Dr. Tony Huang as a postdoctoral fellow, focusing on the role of deubiquitylating enzymes (DUBs) in the replication stress response. Kate is passionate about oncology research and the development of therapeutic tools to manipulate cell proliferation in cancer treatment.

Dr. Bridon is an R&D executive with extensive North American and international experience of drug development from research to proof-of-concept clinical studies (Phase II) and regulatory submission in EU and US. 20+ years of experience with peptides therapeutics including drug protein bio-conjugate development across multiple therapeutic areas to treat cancer, anti-infective, metabolic and cardiovascular diseases. He previously held various management positions at Optivia (acquired by BioIVT), Ipsen, Abbott, Enobia (acquired by Alexion) and Neuronax and served on the scientific boards of Syntaxin (acquired by Ipsen) and Biosortia. He is currently CEO of Diaccurate, a Paris-based star-up.

Dr. DeVita is an experienced medicinal chemist and drug hunter in academia, biotech and large pharmaceutical environments. He has over 30 years of drug discovery and development experience including expertise managing multi-disciplinary teams to deliver on key program objectives for complex molecular targets. Dr. DeVita started his career at Merck Research Laboratories and rose to Director of Medicinal Chemistry, where he delivered many development candidates and led drug discovery and development teams. Dr. DeVita was also VP of Chemistry at Agios Pharmaceuticals focused on oncology drug discovery. Since 2013, he founded a consulting firm which has consulted for a wide variety of clients including biotechs building translational drug discovery programs. He is also Professor in the Dept. of Pharmacological Sciences and Director of Medicinal Chemistry in the Drug Discovery Institute of Icahn School of Medicine at Mt. Sinai since 2014.

Dr. Janice Lansita is a board-certified toxicologist with over 17 years of experience both in the biopharmaceutical industry and with the Food and Drug Administration (FDA). As a regulatory toxicologist, she has developed small molecule (NME and 505(b)(2)) and biologic therapies for a broad range of indications (e.g., rare disease, oncology, neurology, pain, ophthalmology, and immunology). Dr. Lansita has extensive experience in the design, monitoring, and interpretation of nonclinical toxicology studies (GLP and non-GLP) and has authored the nonclinical sections of various regulatory documents, including pre-INDs, INDs/CTAs (>45), Investigator Brochures, BLAs/NDAs, and package inserts/product labels for biopharmaceuticals.

Dr. Wu is an Associate Professor in the Department of Biomedical Engineering at University at Buffalo, The State University of New York (SUNY Buffalo). Her research focuses on the development of nanotherapeutics for cancer and chronic diseases and the development of in vitro diagnostic tests for cancer screening, diagnosis and prognosis. She received her Ph.D. from the Department of Chemical and Biomolecular Engineering at the Ohio State University in 2009. After completion of her degree, she received her postdoc training in the NSF Nanoscale Science and Engineering Center at the Ohio State University.

Natalie graduated in May 2023 from Villanova University where she majored in Chemical Engineering with a minor in Biochemical Engineering. In her time at Villanova, under the direction of Dr. Noelle Comolli and in partnership with Merck, she completed her senior thesis on the Synthesis and Characterization of Antibody Drug Conjugates. Through this she gained a variety of knowledge, experience, and a passion for pursuing less toxic cancer treatments.