“Nadia brings an impressive degree of relevant commercial experience with prior leadership roles in marketing and sales at global biopharmaceutical companies, including a track record of successfully launching multiple novel neurology products in competitive markets,” said
Ms. Dac brings more than 25 years of U.S. and global commercial experience with both large and small publicly traded biopharmaceutical companies, with extensive expertise across all commercial functions including marketing, market access and promotion, sales, pipeline management, business development and partnerships. She joins Alder from
“I’m thrilled to join the Alder team at such an exciting and pivotal moment for the company and the migraine community, as the company has the potential to transform the treatment paradigm for migraine patients,” said Ms. Dac. “I look forward to working with the Alder team as we prepare for the expected approval and launch of eptinezumab in the first quarter of 2020, and to contribute to the growth of Alder as it scales the organization into a fully integrated biopharmaceutical company.”
This press release contains forward-looking statements, including, without limitation, statements relating to: the potential approval, launch and commercialization of eptinezumab; the advancement of Alder’s pipeline; Alder’s potential to transform the treatment paradigm for migraine patients; and Alder’s continued growth into a fully integrated biopharmaceutical company. Words such as “will,” “continue,” “prepare,” “advance,” “potential,” “transform,” “look forward,” “expected,” “contribute,” “growth,” “scales,” or other similar expressions, identify forward-looking statements, but the absence of these words does not necessarily mean that a statement is not forward-looking. In addition, any statements that refer to expectations, projections or other characterizations of future events or circumstances are forward-looking statements. The forward-looking statements in this press release are based upon Alder's current plans, assumptions, beliefs, expectations, estimates and projections, and involve substantial risks and uncertainties. Actual results and the timing of events could differ materially from those anticipated in the forward-looking statements due to these risks and uncertainties as well as other factors, which include, without limitation: the clinical, therapeutic and commercial value of eptinezumab; risks and uncertainties related to regulatory application, review and approval processes and Alder's compliance with applicable legal and regulatory requirements; risks and uncertainties relating to the build of Alder’s commercialization infrastructure; risks and uncertainties relating to the manufacture and supply of eptinezumab; Alder’s ability to develop and advance programs in its pipleline; Alder's ability to obtain and protect intellectual property rights, and operate without infringing on the intellectual property rights of others; the uncertain timing and level of expenses associated with Alder's development and commercialization activities; the sufficiency of Alder's capital and other resources; market competition; changes in economic and business conditions; and other factors discussed under the caption "Risk Factors" in Alder's Annual Report on Form 10-K for the fiscal year ended
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Source: Alder BioPharmaceuticals, Inc.