CepTor Redeems 2.9 Million Shares from Xechem; Cancelled Shares Represent 24% Accretion to CepTor Shareholders.HUNT VALLEY, Md. -- CepTor Corporation, Inc. (OTC OTC See: Over-the-counter. OTC See over-the-counter market (OTC). BB:CEPO CEPO County Emergency Planning Officer (UK) CEPO Community & Environment Project Office (Edmonton Green, North London) ) today announced that it has redeemed 85% of the shares held by Xechem International, Inc. which will subsequently be cancelled, representing, on an issued and outstanding basis, an anti-dilution of approximately 24%. CepTor purchased 2,886,563 shares of CepTor stock from Xechem for cash at a discount to market. The Agreement cancels any obligations by CepTor to use proceeds from future financings to redeem CepTor shares held by Xechem. As part of the Agreement, William Pursley, Chairman and CEO (1) (Chief Executive Officer) The highest individual in command of an organization. Typically the president of the company, the CEO reports to the Chairman of the Board. of CepTor, surrendered 43,000,000 personally owned options to purchase Xechem shares at $0.0025 per share. Xechem will retain just 500,000 restricted shares of CepTor stock, representing about 4% of CepTor shares outstanding, that can only be sold under Rule 144 volume restrictions. Regarding the transaction, Mr. Pursley stated, "This represents a very healthy long-term move for the Company. We believe our current and future shareholders will benefit in many ways: shareholders enjoy an immediate 24% accretion on their ownership positions; the elimination of nearly a 3.4 million share overhang held by a non-strategic owner provides stability; it terminates over $700,000 of redemption obligations the Company had with Xechem related to future financings and; it eliminates a reportable and beneficial owner Beneficial Owner A person who enjoys the benefits of ownership even though title is in another name. Notes: For example, when shares of a mutual fund are held by a custodian bank or when securities are held by a broker in street name, the true owner is the beneficial . "As far as the return of my own options to Xechem," Pursley continued, "It reveals my willingness to put CepTor's best interests before my own and should be viewed as an indication of my confidence in CepTor's current and future prospects." About CepTor CepTor Corporation is a development-stage biopharmaceutical company engaged in the discovery, development, and commercialization of proprietary, cell-targeted therapeutic products for the treatment of neuromuscular neuromuscular /neu·ro·mus·cu·lar/ (-mus´ku-ler) pertaining to nerves and muscles, or to the relationship between them. neu·ro·mus·cu·lar adj. 1. and neurodegenerative diseases neurodegenerative diseases diseases characterized by neurodegeneration. Lesions are microscopic only but in chronic disease with massive involvement there may be grossly visible atrophy of affected nervous tissue. with a focus on orphan diseases. The Company's mission is to increase the quality and quantity of life of people suffering with these diseases. An orphan disease is defined in the United States United States, officially United States of America, republic (2005 est. pop. 295,734,000), 3,539,227 sq mi (9,166,598 sq km), North America. The United States is the world's third largest country in population and the fourth largest country in area. as a serious or life-threatening disease that affects less than 200,000 people and for which no definitive therapy currently exists. CepTor Corporation seeks to create an efficient orphan drug orphan drug, drug developed under the U.S. Orphan Drug Act (1983) to treat a disease that affects fewer than 200,000 people in the United States. The orphan drug law offers tax breaks and a seven-year monopoly on drug sales to induce companies to undertake the platform by taking advantage of the legislative, regulatory and commercial opportunities common to these rare diseases. CepTor's primary efforts are currently being focused on moving its lead product, MYODUR, into phase I/II clinical trials for Duchenne's muscular dystrophy Duchenne's muscular dystrophy, n an X-linked recessive condition pres-ent at birth in which the muscles of the pelvis and legs waste away in a symmetric fashion. . The Company's broad platform technology also includes the development of products for multiple sclerosis, retinal degeneration and epilepsy. This news release contains forward-looking statements. Such statements are valid only as of today, and we disclaim any obligation to update this information. These statements are subject to known and unknown risks and uncertainties that may cause actual future experience and results to differ materially from the statements made. These statements are based on our current beliefs and expectations as to such future outcomes. Drug discovery and development involve a high degree of risk. Factors that might cause such a material difference include, among others, uncertainties related to the ability to attract and retain partners for our technologies, the identification of lead compounds, the successful preclinical development thereof, the completion of clinical trials, the 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. review process and other government regulation, our pharmaceutical collaborator's ability to successfully develop and commercialize drug candidates, competition from other pharmaceutical companies, product pricing and third party reimbursement. |
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