ImmunoGen Appoints Stuart A. Arbuckle to Board of Directors
“We are grateful for Howard’s many contributions to ImmunoGen over the
last eight years,” stated
“Stuart joins ImmunoGen’s Board at a pivotal moment in the Company’s evolution,” Mr. McCluski continued. “His international commercial expertise will be vital as we continue to advance mirvetuximab soravtansine in the FORWARD I registration trial, accelerate the development of our earlier-stage ADC assets, and evolve into a business with marketed products.”
Mr. Arbuckle has more than 30 years of experience in building
biopharmaceutical commercial organizations and has served as Vertex’s
Executive Vice President and Chief Commercial Officer since 2012,
leading the successful global launches of Kalydeco® and
Orkambi®. Prior to joining Vertex, Mr. Arbuckle held multiple
commercial leadership roles at
Mr. Arbuckle stated, “ImmunoGen embarked on a journey last year to focus on its highest value programs and develop into a fully integrated biotech company. I’m delighted to offer my insights and work with this Board as ImmunoGen drives long-term value creation and moves towards commercializing its first product.”
About
ImmunoGen is a clinical-stage biotechnology company that develops
targeted cancer therapeutics using its proprietary ADC technology. The
Company’s lead product candidate, mirvetuximab soravtansine, is in a
Phase 3 trial for FRα-positive platinum-resistant ovarian cancer, and is
in a Phase 1b/2 trial in combination regimens for earlier-stage disease.
ImmunoGen has three additional clinical-stage product candidates, two of
which are being developed in collaboration with
Kalydeco®, Orkambi®, Aranesp®, Neulasta®, NEUPOGEN®, XGEVA®, Nplate®, and Kadcyla® are registered trademarks of their respective owners.
This press release includes forward-looking statements. 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. It should be noted that there are risks and
uncertainties related to the development of novel anticancer products,
including risks related to preclinical and clinical studies, their
timings and results. A review of these risks can be found in ImmunoGen's
Transition Report on Form 10-KT for the six-month transition period
ended
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