Biovail Board Approves Stock-Repurchase Program.Business Editors and Health/Medical Writers TORONTO--(BW HealthWire)--Sept. 17, 2001 Biovail Corporation (NYSE NYSE See: New York Stock Exchange :BVF BVF Biovail Corporation (stock symbol) BVF Berufsverband der Frauenärzte eV (Muenchen, Germany) BVF Bearing Versus Frequency ) (TSE See Tokyo Stock Exchange. TSE 1. See Tokyo Stock Exchange (TSE). 2. See Toronto Stock Exchange (TSE). :BVF) -- Board of Directors approves repurchase of up to $120 million of Biovail's outstanding common shares. -- Board of Directors appoints Eugene Melnyk as Co-Chief Executive Officer. -- Bruce Brydon appointed Executive Director of Biovail Ventures and continues as Co-Chief Executive Officer. Biovail Corporation (NYSE:BVF) (TSE:BVF) today announced that its Board of Directors has authorized the Company to implement a Stock-Repurchase Program pursuant to which the Company may repurchase up to $120 million of its issued and outstanding common stock, depending on market conditions and other factors. The common stock will be purchased through open market transactions on the New York Stock Exchange New York Stock Exchange (NYSE) World's largest marketplace for securities. The exchange began as an informal meeting of 24 men in 1792 on what is now Wall Street in New York City. in accordance with applicable rules and regulations. Biovail has approximately 141.6 million common shares outstanding. Separately, the Board of Directors has formally appointed Chairman of the Board, Eugene Melnyk Eugene Melnyk (born May 27, 1959 in Toronto, Ontario) is a Canadian businessman of Ukrainian origin who now resides in Barbados. He is the chairman and chief executive officer of Biovail Corporation. , as Co-Chief Executive Officer along with Bruce Brydon. In addition to acting as Co-Chief Executive Officer, Mr. Brydon has been appointed Executive Director of Biovail Ventures. Biovail Ventures was established in January 2000 with a mandate to broaden the Company's commercial relationships including the licensing of product rights and complementary technologies as well as research relationships with emerging pharmaceutical, healthcare and life sciences companies. Bruce Brydon commented, "We are seeing numerous product licensing and investment opportunities in therapeutic categories which are of strategic interest to Biovail. This includes cardiovascular, pain management, diabetes and oncology products. Several of these opportunities are in late stage discussions and, subject to successful negotiations, will provide strategic benefits to Biovail over the coming years." Eugene Melnyk commented, "Biovail is currently expanding its base business including the significant expansion of its North American North American named after North America. North American blastomycosis see North American blastomycosis. North American cattle tick see boophilusannulatus. sales force in support of the pending launch of Cardizem XL and other pharmaceutical brands. The combination of Biovail's maturing branded product pipeline portfolio and the numerous strategic investment opportunities with resulting residual product a by product, as cotton waste from a cotton mill, coke and coal tar from gas works, etc. See also: Residual rights will allow the Company to better leverage it's sales force and fully maximize its business potential." Biovail Corporation is an international full-service pharmaceutical company, engaged in the formulation, clinical testing, registration, manufacture, sale and promotion of pharmaceutical products utilizing advanced drug delivery technologies. "Safe Harbor Safe Harbor 1. A legal provision to reduce or eliminate liability as long as good faith is demonstrated. 2. A form of shark repellent implemented by a target company acquiring a business that is so poorly regulated that the target itself is less attractive. " statement under the Private Securities Litigation Reform Act The Private Securities Litigation Reform Act of 1995 (PSLRA) implemented several significant substantive changes affecting certain cases brought under the federal securities laws, including changes related to pleading, discovery, liability, class representation and awards fees and of 1995. To the extent any statements made in this release contain information that is not historical, these statements are essentially forward looking and are subject to risks and uncertainties, including the difficulty of predicting FDA FDA abbr. Food and Drug Administration FDA, n.pr See Food and Drug Administration. FDA, n.pr the abbreviation for the Food and Drug Administration. approvals, acceptance and demand for new pharmaceutical products, the impact of competitive products and pricing, new product development and launch, reliance on key strategic alliances, availability of raw materials, the regulatory environment, fluctuations in operating results and other risks detailed from time to time in the company's filings with the Securities and Exchange Commission. |
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