Healthcare Industry News: Insmed
News Release - June 25, 2007
Experienced Biopharmaceutical Executive Steve Glover Joins Insmed; Will Lead Development of Follow-on BiologicsRICHMOND, Va.--(HSMN NewsFeed)--Insmed Inc. (Nasdaq:INSM ) today announced that Steve Glover, 48, has joined Insmed's management team as President of the newly formed Follow-on Biologics business, effective June 22, 2007. Mr. Glover will be responsible for leading the development of Insmed's follow-on biologics capability and its emerging portfolio of biogeneric/biosimilar products.
Mr. Glover commented, "I am excited to join the talented management team that Insmed has assembled -- a team able to leverage Insmed's advanced knowledge of biologics development, its manufacturing capability, and its skilled scientific and technical workforce to make it the first U.S.-based biotechnology company to develop a comprehensive portfolio of follow-on biologics. This is an organization that knows the drug industry is on the threshold of its second generic revolution."
Dr. Geoffrey Allan, President and Chief Executive Officer of Insmed, commented, "We are looking forward to benefiting from Steve's extensive leadership experience in the bio-pharmaceutical and life sciences sectors. His expertise will be instrumental in providing the strategic direction and tactical capability to take full advantage of our unique combination of protein know-how and drug approval skills. He will play a pivotal role in our follow-on biologics strategy, which together with the development of our approved flagship product IPLEX(TM) in niche markets, forms a dual-path approach for success."
Insmed is a bio-pharmaceutical company focused on the development and approval of drugs for the treatment of metabolic diseases with unmet medical needs. For more information, please visit www.Insmed.com. To be added to Insmed's investor lists, please contact Haris Tajyar at email@example.com or at 818-382-9702.
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, the Company may lack financial resources to complete development of product candidates, the FDA may interpret the results of studies differently than the Company, competing products may be more successful, demand for new pharmaceutical products may decrease, the bio-pharmaceutical industry may experience negative market trends, and other risks and challenges detailed in the Company's filings with the U.S. Securities and Exchange Commission, including the Company's Quarterly Report on Form 10-Q for the quarter ended March 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. The Company undertakes 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.
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