Dr. John Krystal
Dr. John Krystal is best known for the discovery of the rapid antidepressant effects of ketamine in patients (2000) and the invention of Esketamine, which directly led to FDA approval of Jannsen’s Spravato Esketamine spray, the first novel antidepressant in 50 years (Esketamine, 2019). John is also one of the top experts in the neurobiology and treatment of alcoholism and PTSD. Most recently, he co-founded the National PTSD Brain Bank and co-led the first transcriptomic studies of PTSD.
Dina Burkitbayeva
Dina Burkitbayeva is a serial entrepreneur and a co-founder at PsyMed Ventures, venture fund focused on cutting edge mental health treatments including psychedelic therapeutic, neurotechnology, precision psychiatry and digital therapeutics. Dina holds an MBA from Harvard Business School and is working towards her PhD in East West Psychology with a focus on psychedelic therapy at California Institute of Integral Studies.
Dr. Robert Berman
Dr. Robert Berman first discovered the antidepressant effects of ketamine in humans alongside Dr John Krystal in 1990s at Yale. For over 20 years he has worked within the industry, first at Pfizer and then Bristol-Myers Squibb in clinical development roles, including leading the program for aripiprazole in depression, for which he developed novel clinical trial design that achieved three out of three highly statistically significant trials. In 2013, Rob co-founded Biohaven Pharmaceuticals (NYSE:BHVN) and was Chief Medical Officer until 2019.
Dr. David Hough
David Hough, MD is the Chief Medical Officer at Freedom Biosciences. Prior to joining Freedom, Dr. Hough spent 17 years in various leadership roles at Janssen Research and Development, LLC (a Johnson & Johnson company). Most recently, he was the leader of the compound development team working on Spravato (esketamine).
Dr. Janice Lansita
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).
Lizzy Sands
Lizzy Sands is an experienced leader in both health and wellness operations. Her work in clinical practice as a nutritionist evolved into that of operator, and she has worked in a range of settings spanning the healthcare and wellness spaces. From functional medicine, concierge medicine and wellness, to chronic care management and beyond, her focus is on developing sustainable solutions that drive patient care forward.
Dr. Julie Straub
Dr Julie Straub directs Freedom Bio’s nonclinical development and chemistry, manufacturing and controls (CMC) and formulation efforts on a consulting basis. She is an experienced pharmaceutical development consultant working with a range of development stage pharmaceutical and biotech companies from concept through FDA marketing approval for a variety of products.