ImmunoGen Appoints Mimi Huizinga, MD, as Senior Vice President and Head of Medical Affairs
“As evidence generation and stakeholder engagement play increasingly important roles in delivering innovative therapies to patients, Medical Affairs has evolved to a third strategic pillar of our business, alongside R&D and Commercial,” said
“I am excited to join ImmunoGen at such an important time, and to lead a growing global Medical Affairs function that supports the launch of our pivotal programs and the development of our earlier stage assets,” said
ImmunoGen is developing the next generation of antibody-drug conjugates (ADCs) to improve outcomes for cancer patients. By generating targeted therapies with enhanced anti-tumor activity and favorable tolerability profiles, we aim to disrupt the progression of cancer and offer our patients more good days. We call this our commitment to TARGET A BETTER NOW™.
Learn more about who we are, what we do, and how we do it at www.immunogen.com.
This press release includes forward-looking statements based on management's current expectations. These statements include, but are not limited to, ImmunoGen's expectations related to: the occurrence, timing, and outcome of regulatory events related to the Company's product candidates, in particular with respect to mirvetuximab soravtansine, and the launch of mirvetuximab soravtansine in the second half of 2022; and the Company’s business and product development of novel ADCs. For these statements, ImmunoGen claims the protection of the safe harbor for forward-looking statements provided by the Private Securities Litigation Reform Act of 1995. Various factors could cause ImmunoGen's actual results to differ materially from those discussed or implied in the forward-looking statements, and you are cautioned not to place undue reliance on these forward-looking statements, which are current only as of the date of this release. Factors that could cause future results to differ materially from such expectations include, but are not limited to: the timing and outcome of the Company's preclinical and clinical development processes; the difficulties inherent in the development of novel pharmaceuticals, including uncertainties as to the timing, expense, and results of preclinical studies, clinical trials, and regulatory processes, including approval of the Company’s biologics license application for mirvetuximab soravtansine; the Company's ability to financially support its product programs; risks and uncertainties associated with the scale and duration of the COVID-19 pandemic and the resulting impact on ImmunoGen's industry and business; and other factors as set forth in the Company's Annual Report on Form 10-K filed with the
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