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Radius Provides Agenda for Today's R&D Webcast
BOSTON, April 05, 2022 (GLOBE NEWSWIRE) -- Today, Radius Health, Inc. (“Radius” or the “Company”) (NASDAQ: RDUS) will host its Neuroscience R&D webcast to discuss RAD011, our investigational synthetic cannabidiol oral solution with potential utilization in multiple neuro-endocrine, neurodevelopmental, or neuropsychiatric disease areas. The webcast will be held from 10:00am to 12:00pm ET allowing for 1.5 hours of presentations and 30-minutes for Q&A. The following topics will be covered during the webcast: Science, Data and Clinical Translation Seizures: Angelman syndrome Hyperphagia: Prader-Willi syndrome Orphan Designation and IP Competitive Landscape and Market Dynamics Webcast and Conference Call Information Date: April 5, 2022 A live audio webcast of the call can be accessed from the Investors section of the Company’s website, www.radiuspharm.com. A replay of the event will be available on April 5 at 3:00pm ET and the audio webcast of the call will be archived on the Company's website for ninety days. To access the replay, dial (855) 859-2056 or (404) 537-3406 for International, using conference ID number 9678881. The live audio webcast of the call can be accssed from the Investors section of the Company’s website, https://ir.radiuspharm.com/events-and-presentations. About Radius About RAD011 Forward-Looking Statements These forward-looking statements are based on management's current expectations. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, the following: the adverse impact the ongoing COVID-19 pandemic is having and is expected to continue to have on our business, financial condition and results of operations, including our commercial operations and sales, clinical trials, preclinical studies, and employees; quarterly fluctuation in our financial results; our dependence on the success of TYMLOS, and our inability to ensure that TYMLOS will obtain regulatory approval outside the U.S. or be successfully commercialized in any market in which it is approved, including as a result of risk related to coverage, pricing and reimbursement; risks related to competitive products; risks related to our ability to successfully enter into collaboration, partnership, license or similar agreements; risks related to clinical trials, including our reliance on third parties to conduct key portions of our clinical trials and uncertainty that the results of those trials will support our product candidate claims; the risk that adverse side effects will be identified during the development of our product candidates or during commercialization, if approved; risks related to manufacturing, supply and distribution; and the risk of litigation or other challenges regarding our intellectual property rights. These and other important risks and uncertainties discussed in our filings with the Securities and Exchange Commission, or SEC, including under the caption “Risk Factors” in our Annual Report on Form 10-K for the year ending December 31, 2021 and subsequent filings with the SEC, could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management's estimates as of the date of this press release. While we may elect to update such forward-looking statements at some point in the future, we disclaim any obligation to do so, even if subsequent events cause our views to change. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date of this press release. Investor & Media Relations Contact: |