CAMBRIDGE, Mass.– Tessera Therapeutics, the biotechnology company pioneering GENE WRITING™ technology, today announced the appointment of Anne-Virginie Eggimann, M.Sc. as Chief Regulatory Officer (CRO) responsible for leading U.S. and global regulatory science and program and portfolio management for the company’s GENE WRITING development programs. Additionally, former CVS Health and Eli Lilly executive Derica Rice has joined the company’s Board of Directors.
Ms. Eggimann joins Tessera from bluebird bio where she spent nearly eleven years guiding regulatory strategy for the company’s gene therapy portfolio, culminating in her role as Chief Regulatory Officer. During her tenure, Ms. Eggimann oversaw cross-disciplinary teams responsible for identifying efficient development pathways leading to several U.S. and EU approvals for three novel gene therapy products in severe genetic diseases and oncology, including most recently the approval of ZYNTEGLO, the first lentiviral vector gene therapy in the U.S. for the treatment of beta-thalassemia. In parallel, she has also contributed to shaping U.S. regulatory policy for advanced therapies as chair of the Regulatory Committee of the Alliance for Regenerative Medicine (ARM) and currently as the co-chair of the Biotechnology Innovation Organization (BIO) Regenerative Medicine Committee where she recently participated in the PDUFA VII negotiations with industry trade associations BIO and PhRMA and the FDA.
“Genetic medicines hold tremendous potential to cure diseases and, as the field rapidly evolves, so does the regulatory environment that opens doors to these life-changing medicines for patients,” said Ms. Eggimann. “Tessera’s GENE WRITING technology is exceptionally compelling to me for its potential to leapfrog innovation in genetic medicine and broadly address diseases that have so far proven elusive to cell and gene therapies. These attributes, coupled with the strength of the current leadership team and improvements in delivery and manufacturing that are designed to make these potentially curative treatments more accessible to patients around the world, made joining Tessera in this capacity an irresistible opportunity.”
“Anne-Virginie has proven herself to be an adept and agile leader who has a proven track record of skillfully navigating unchartered territory to bring new platform technologies to market and building high-functioning teams,” said Michael Severino, M.D., Tessera’s Chief Executive Officer. “Her deep expertise in U.S. and global regulatory strategy combined with her entrepreneurial mindset make her an excellent addition to the leadership team.”
Mr. Rice brings to Tessera’s board vast pharmaceutical and healthcare leadership experience, having led the pharmacy benefits management business of CVS Health and served as Chief Financial Officer at Eli Lilly. Mr. Rice also serves on the boards of Bristol Myers Squibb, The Carlyle Group, Target and Disney.
“Derica is an exceptional leader and champion for innovative therapies with the potential to transform human health,” said Geoffrey von Maltzahn, Ph.D., Tessera’s co-founder and board chair. “Derica’s intimate knowledge of the commercial and payor landscape will be vital as Tessera brings GENE WRITING products to patients and ensures that they are both effective and accessible to those who need them.”
Ms. Eggimann’s and Mr. Rice’s appointments coincide with Tessera’s continued growth. In the last year, Tessera announced the expansion of its Senior Leadership team with the appointments of Michael Severino, M.D., Chief Executive Officer and Board Director, Howard Liang, Ph.D., President and Chief Financial Officer; David Davidson, M.D., Chief Medical and Development Officer; Michael Holmes, Ph.D., Chief Scientific Officer; Iain McFadyen, Ph.D., Chief Data Officer; and Becky Lillie, Chief Human Resources Officer. In April, Tessera announced that it raised over $300 million in Series C financing to advance its GENE WRITING platform.
Tessera’s GENE WRITING technology consists of multiple platforms designed to offer scientists and clinicians the ability to write therapeutic messages into the human genome, thereby curing diseases at their source.
