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Fun City Popcorn, Inc. Enters Into Merger Agreement With Lev Pharmaceuticals, Inc.


DENVER -- Fun City Popcorn, Inc. (OTCBB OTCBB

See OTC Bulletin Board (OTCBB).
: FNCY) announced today that it has executed an agreement and plan of merger to acquire all of the outstanding common stock of privately held Lev Pharmaceuticals, Inc. Closing of the merger is anticipated in December 2004 and is subject to, among other things, stockholder approval by the shareholders of Lev.

Pursuant to the merger agreement, Lev shareholders will receive 5,250,928 shares of Fun City common stock and 5,000,000 shares of Fun City convertible preferred stock Convertible Preferred Stock

Preferred stock that includes an option for the holder to convert the preferred shares into a fixed number of common shares, usually anytime after a predetermined date. Also known as "convertible preferred shares".
. Each share of convertible preferred stock is automatically convertible into 13.940688 shares of Fun City common stock upon approval by the stockholders of Fun City of an increase in the authorized common stock of Fun City to 150,000,000 shares. As a result, on a fully diluted basis including the issuance of all common stock, the conversion of preferred stock Stock shares that have preferential rights to dividends or to amounts distributable on liquidation, or to both, ahead of common shareholders.

Preferred stock is given preference over common stock. Holders of preferred stock receive dividends at a fixed annual rate.
, and allowing for the exercise of all options, and warrants, an aggregate of 79,459,898 shares will be outstanding upon closing, with current Lev shareholders retaining a 94.33% ownership of Fun City and the current Fun City shareholders retaining 5.67%.

Lev is a biopharmaceutical company focused on developing and commercializing therapeutic products for the treatment of inflammatory diseases. Lev's product candidates are based on C1-esterase inhibitor ("C1-INH"), a human plasma protein plasma protein
n.
Any of the various dissolved proteins of blood plasma, including antibodies and blood-clotting proteins, that act by holding fluid in blood vessels by osmosis.
 that mediates inflammation and is potentially applicable as a treatment for a range of medical indications. Lev is developing C1-INH for the treatment of hereditary angioedema Hereditary angioedema
A complement deficiency characterized by lymphatic vessel blockages that cause temporary swelling (edema) of areas of the skin, mucous membranes, and, sometimes, internal organs.

Mentioned in: Complement Deficiencies
 ("HAE"), acute myocardial infarction acute myocardial infarction (·kyōōtˑ mī·ō·karˑ·dē· , or heart attack, and other diseases and disorders in which inflammation is known or believed to play an underlying role.

HAE is a rare genetic disorder characterized by episodic attacks of edema edema (ĭdē`mə), abnormal accumulation of fluid in the body tissues or in the body cavities causing swelling or distention of the affected parts.  (swelling) in various parts of the body -- the face, the extremities, the abdominal wall, and, most seriously, the airway passages, which, if left untreated, can be fatal. The disease is caused by a deficiency of functional C1-INH, and there are approximately 10,000 patients with HAE in the United States. In Europe, C1-INH, produced by other manufacturers, has been used to treat patients with HAE for more than 30 years.

In the third quarter of 2004, Lev filed an Investigational New Drug Application with the U.S. 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.
") to begin a Phase III clinical trial Noun 1. phase III clinical trial - a large clinical trial of a treatment or drug that in phase I and phase II has been shown to be efficacious with tolerable side effects; after successful conclusion of these clinical trials it will receive formal approval from the  of C1-INH for the treatment of HAE, and the Company expects to initiate this Phase III clinical trial during the first half 2005. In July 2004, Lev received orphan drug designation from the FDA for C1-INH (human), which, upon product licensure, could provide the Company with a seven-year exclusive right to market its C1-INH product as an HAE treatment in the United States.

Judson Cooper, Chairman of Lev, said: "Based on the long European clinical experience, C1-INH is accepted by HAE associations around the world as the treatment of choice for this serious disorder. It can be used to treat acutely, when there is an HAE attack, or prophylactically, to prevent attacks, depending on the severity of the case. Our primary objective is to bring C1-INH to the United States for the many patients suffering from this disorder."

In commenting on the merger, Jim Eller, President of Fun City, said: "I could not be more excited about the prospects for our shareholders in this transaction. Lev looks to have a very viable Phase III-status first product with good additional product prospects beyond that."

Upon completion of the merger, it is anticipated that the name of Fun City will be changed to Lev Pharmaceuticals, Inc. Additional information can be accessed through Fun City Popcorn, Inc.'s November 10, 2004, 8K filing on Edgar at sec.gov.

Safe Harbor Statement

Information included in this news release contains forward-looking statements made pursuant to 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 ("Reform Act"). Such statements are based on current expectations and involve a number of known and unknown risks and uncertainties that could cause the actual results and performance of the Company to differ materially from any expected future results or performance, expressed or implied, by the forward-looking statements. In connection with the safe harbor provisions of the Reform Act, Fun City has identified important factors that could cause actual results to differ materially from such expectations, including operating uncertainties, uncertainties relating to economic issues and competition. Reference is made to all of the Company's SEC filings, including the Company's Reports on Forms 10KSB KSB Kogod School of Business (American University)
KSB Kelley School of Business (Indiana University)
KSB Kantonsschule Am Brühl St.
, 10QSB QSB Fading
QSB Qualified Small Business (IRS category)
QSB Queen Street Backpackers (Auckland, New Zealand)
QSB Quality System Basics
QSB Qualified Supplemental Benefit
QSB Quantum Singleton Bound
 and other periodic reports.
COPYRIGHT 2004 Business Wire
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2004, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Publication:Business Wire
Date:Nov 17, 2004
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