Sage Therapeutics Appoints Jessica Federer to Board of Directors
Sage Therapeutics, Inc. (NASDAQ: SAGE) has appointed Jessica Federer to its Board of Directors. With a strong background in digital health and innovation, Federer aims to enhance the company's growth in maternal mental health care. She previously served as the first Chief Digital Officer for Bayer AG, where she shaped global digital strategy. Federer expressed her commitment to redefining brain health treatment, highlighting the potential of data strategies in this area. CEO Barry Greene noted her patient-first approach aligns with Sage's core values and ambitions. This strategic appointment could drive future growth for the company.
- Appointment of Jessica Federer as a Board member expected to enhance corporate growth.
- Federer's expertise in digital health and innovation aligns with Sage's focus on maternal mental health.
- Strategic leadership change aimed at bolstering growth in critical health areas.
- None.
“We are thrilled to have Jessica join our Board of Directors. Jessica is a champion for patients and has a track record of innovation in data and digital transformation which will be a key future growth driver for the industry,” said
“I’m honored to join the Sage Board of Directors at such an incredibly exciting time. Sage has led the way in maternal mental health care, an area of great need and one that is particularly important to me. I’m looking forward to supporting the company’s goal of redefining how we think about and treat a wide range of brain health conditions. I see the vast potential for data and digital strategies in the brain health area,” said
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Forward-Looking Statements
Various statements in this release concern Sage's future expectations, plans and prospects, including without limitation: our views and expectations regarding our goals, opportunity, plans, mission and potential for our programs, strategies and business. These statements constitute forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. These forward-looking statements are neither promises nor guarantees of future performance, and are subject to a variety of risks and uncertainties, many of which are beyond our control, which could cause actual results to differ materially from those contemplated in these forward-looking statements, including the risks that: the FDA may ultimately decide that the design or results of our completed, ongoing and planned clinical trials for any of our product candidates, even if positive, are not sufficient for regulatory approval in the indications that are the focus of our efforts; other decisions or actions of the FDA or other regulatory agencies may affect the regulatory paths for our product candidates or the initiation, timing, design, size, progress and cost of clinical trials and our ability to proceed with further development; success in our earlier clinical trials or non-clinical studies may not be repeated or observed in ongoing or future studies, and ongoing and future clinical and non-clinical results may not meet their primary or key secondary endpoints or support further development; we may encounter adverse results or adverse events in use of our products or product candidates that negatively impact further development, our ability to obtain regulatory approval or our commercialization plans or that require additional nonclinical and clinical work which may not yield positive results; the unmet need for additional treatment options, the impact of our planned strategies, our ability to change treatment paradigms, and the potential for our current or future products, may be significantly smaller than we expect; we may encounter technical and other unexpected hurdles in the development and manufacture of our product candidates or commercialization of any of our products which may delay our timing or change our plans or increase our costs; as well as those risks more fully discussed in the section entitled "Risk Factors" in our most recent Quarterly Report on Form 10-Q, as well as discussions of potential risks, uncertainties, and other important factors in our subsequent filings with the
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