RICHMOND, Va., Nov 18, 2008 /PRNewswire-FirstCall via COMTEX News Network/ --
Insmed Inc. (Nasdaq: INSM) a developer of follow-on biologics and biopharmaceuticals, today announced that Geoffrey Allan, Ph.D., CEO of Insmed, will participate in the Federal Trade Commission Roundtable on Follow-on Biologic Drugs: Framework for Competition and Continued Innovation taking place on Friday, November 21, 2008, in Washington D.C.
Dr. Allan will take part in two roundtable discussion panels at the event. The first, entitled Likely Competitive Effects of Reference Product Regulatory Exclusivity, will be a discussion of the economic model to assess the pros and cons of any regulatory exclusivity period from both the innovator firms' and FOB applicants' perspectives. The second, entitled Follow-on Biologic Regulatory Incentives, will be a discussion of whether there is a need to provide regulatory incentives for the filing of FOB applications.
Insmed Inc. is a biopharmaceutical company with unique protein process development and manufacturing experience and a proprietary protein platform aimed at niche markets with unmet medical needs. For more information, please visit www.insmed.com.
This release contains forward-looking statements which are made pursuant to provisions of Section 21E of the Securities Exchange Act of 1934. Investors are cautioned that such statements in this release, including statements relating to planned clinical study design, regulatory and business strategies, plans and objectives of management and growth opportunities for existing or proposed products, constitute forward-looking statements which involve risks and uncertainties that could cause actual results to differ materially from those anticipated by the forward-looking statements. The risks and uncertainties include, without limitation, risks that product candidates may fail in the clinic or may not be successfully marketed or manufactured, we may lack financial resources to complete development of product candidates, the FDA may interpret the results of studies differently than us, competing products may be more successful, demand for new pharmaceutical products may decrease, the biopharmaceutical industry may experience negative market trends, our entrance into the follow on biologics market may be unsuccessful, our common stock could be delisted from the Nasdaq Capital Market and other risks and challenges detailed in our filings with the U.S. Securities and Exchange Commission, including our Annual Report on Form 10-K for the year ended December 31, 2007. Readers are cautioned not to place undue reliance on any forward-looking statements which speak only as of the date of this release. We undertake no obligation to publicly release the results of any revisions to these forward-looking statements that may be made to reflect events or circumstances that occur after the date of this release or to reflect the occurrence of unanticipated events.