Maha Radhakrishnan, M.D is currently Executive Partner at Sofinnova Investments and in her most recent role was Consultant to the CEO at Dyne Therapeutics helping with the overarching strategy and direction to the company R&D and Commercialization efforts. Prior to that she was the Chief Medical Officer at Biogen, responsible for the Worldwide Medical function since rejoining Biogen in January 2020. Previously, from 2016-2019, Dr. Radhakrishnan was Senior Vice President and Global Head of Medical, Primary Care Business Unit at Sanofi, a global biopharmaceutical company focused on human health. At Sanofi, she led the medical strategy and operations for the diabetes and cardiovascular products and development programs. Prior to this, she held several key leadership roles at Bioverativ Inc. from 2016-2018, Biogen for the first time from 2013-2016, Bristol Myers Squibb from 2009-2013, United Health Group from 2006-2008, and Cephalon from 2005-2006. Dr. Radhakrishnan has extensive experience in overseeing the medical strategy development, external scientific engagement strategy with academic institutions, top and emerging key opinion leaders, patient advocacy groups, media, investors, payers, policy makers, government, and regulators. She has overseen the launch preparations and execution of several blockbuster launches including Abilify, Orencia, Tecfidera, Praluent, Nusinersen, Qalsody, Leqembi, Skyclarys and Clinical Development including life cycle management of several critical programs in the Hemophilia, Immunology, Rare Disease, Cardiovascular and CNS Therapeutic areas. She received her M.D. in internal medicine with honors from the People’s Friendship University in Moscow, Russia in 1995, as well as a master's degree in Russian language. She is also a certified Russian language instructor and interpreter.
In this session, we will evaluate the investment potential within the rare disease and orphan drug markets, exploring the unique opportunities and challenges these sectors present. Attendees will gain insights into the growing demand for innovative treatments for underserved patient populations and the financial implications of developing therapies for rare conditions. We will also discuss the regulatory landscape, funding trends, and key factors influencing investment decisions. By examining the current investment climate and forecasting future trends, this session aims to provide a comprehensive understanding of how to navigate and capitalize on the evolving rare disease and orphan drug landscape.