Class Action Filed Against Amylin Pharmaceuticals, Inc. On Behalf Of Shareholders Who Purchased Amylin Securities Between February 8, 2000 and July 25, 2001 by the Law Firm of Stull, Stull & Brody.Business Editors & Legal Writers LOS ANGELES--(BUSINESS WIRE)--Aug. 22, 2001 The following statement was issued today by the law firm of Stull, Stull & Brody: A class action lawsuit class action lawsuit A lawsuit in which one party or a limited number of parties sue on behalf of a larger group to which the parties belong. For example, investors may bring a class action lawsuit against a brokerage firm that has actively promoted a tax was filed in United States District Court for the Southern District of California The United States District Court for the Southern District of California is the federal district court whose jurisdiction comprises the following counties in California: Imperial and San Diego. , on behalf of purchasers of Amylin Pharmaceuticals Amylin Pharmaceuticals is a biopharmaceutical company based in San Diego, CA, that was founded in 1987. Currently, Amylin produces two drugs, Symlin (pramlintide acetate) and Byetta (exenatide). Amylin also is working on producing a drug based on Leptin. , Inc. ("Amylin" or the "Company") (NASDAQ NASDAQ in full National Association of Securities Dealers Automated Quotations U.S. market for over-the-counter securities. Established in 1971 by the National Association of Securities Dealers (NASD), NASDAQ is an automated quotation system that reports on :AMLN), securities between February 8, 2000 and July 25, 2001, inclusive (the "Class Period"). You may obtain a copy of the complaint from the Court or from Stull, Stull & Brody. The complaint alleges that Amylin and certain of its officers and directors violated the Securities Exchange Act of 1934. Amylin is engaged in the discovery, development and commercialization of potential drug candidates for the treatment of metabolic disorders. The complaint alleges that on July 25, 2001, the Food and Drug Administration ("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. ") released medical and statistical reviews regarding Amylin's diabetes drug pramlintide acetate pramlintide acetate Symlin Pharmacologic class: Synthetic amylin Therapeutic class: Hypoglycemic Pregnancy risk category C FDA Boxed Warning(SYMLIN) prior to an FDA Advisory Committee Meeting scheduled for July 26, 2001. This review cited major concerns regarding the safety and lack of efficacy of SYMLIN. The review stated there were major adverse events upon treatment with SYMLIN and an alarming number of patients that had life altering events relating to hypoglycemia hypoglycemia: see diabetes.hypoglycemia Below-normal levels of blood glucose, quickly reversed by administration of oral or intravenous glucose. Even brief episodes can produce severe brain dysfunction. (low blood glucose level blood glucose level, n level of glu-cose in the bloodstream, normally about 70 to 115 mg/dL after fasting overnight. Higher levels may indicate diseases such as diabetes mellitus. ), including major trauma, accidents and death, many of which apparently were concealed from the safety database, making this database unreliable to the FDA. This hypoglycemic hypoglycemic /hy·po·gly·ce·mic/ (-gli-sem´ik) 1. pertaining to, characterized by, or causing hypoglycemia. 2. an agent that lowers blood glucose levels. side effect was particularly surprising to the FDA and investors, as the Company all along had claimed that one advantage of SYMLIN over insulin was that it did not increase the risk of hypoglycemia. The public announcements and statements made during the Class Period were materially false and misleading when issued in that they falsely portrayed Amylin as a growing, successful, well-managed, law-abiding, well-controlled company, and a leader of its industry, and that it had a highly effective drug, SYMLIN. Plaintiff seeks to recover damages on behalf of class members and is represented by the law firm of Stull, Stull & Brody who has significant experience and expertise in prosecuting class actions on behalf of investors and shareholders. If you are a member of the class described above, you may, no later than October 8, 2001, move the Court to serve as lead plaintiff, if you so choose. In order to serve as lead plaintiff, however, you must meet certain legal requirements. A lead plaintiff is a representative party that acts on behalf of other class members in directing the litigation An action brought in court to enforce a particular right. The act or process of bringing a lawsuit in and of itself; a judicial contest; any dispute. When a person begins a civil lawsuit, the person enters into a process called litigation. . In order to be appointed lead plaintiff, the Court must determine that the class member's claim is typical of the claims of the other class members, and that the class member will adequately represent the class. Under certain circumstances, one or more class members may together serve as "lead plaintiff." Your ability to share in any recovery is not, however, affected by the decision whether or not to serve as a lead plaintiff. You may retain Stull, Stull & Brody, or other counsel of your choice, to serve as your counsel in this action. If you wish to discuss this action or have any questions concerning this notice or your rights or interests with respect to this matter, please contact: Marc L. Godino of Stull, Stull & Brody at 888-388-4605 or via e-mail at mgodino@secfraud.com or on the law firm's web-site at www.secfraud.com. |
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