News Cortex Reports First Quarter Operating Results IRVINE, Calif., (May 10, 2007) Cortex Pharmaceuticals, Inc. (AMEX: COR) reported a net loss of $3,884,000, or $0.10 per share for the quarter ended March 31, 2007 compared with a net loss of $4,560,000, or $0.14 per share for the corresponding prior year period. Results reflect decreased operating expenses, most notably decreased non-cash stock compensation charges due to a decrease in stock options issued during the quarter ended March 31, 2007 relative to the corresponding prior year quarter. Decreased operating expenses also resulted from personnel-related expenses incurred during the prior year period, including amounts for additions to the Company’s scientific staff. The non-cash stock compensation charges include amounts recorded in accordance with Statement of Financial Accounting Standards 123(R) “Share Based Payment” (“SFAS 123R”), as adopted by Cortex starting January 1, 2006. SFAS 123R requires all share based payments to employees, including grants of employee stock options, to be recognized in the financial statements based on their estimated fair values. These stock compensation charges have no impact on the Company’s available cash or working capital. Decreased clinical expenses in the current year period due to the dosage restrictions imposed by the Food and Drug Administration (the “FDA”) on Ampakine® CX717 were offset by increased preclinical development expenses for follow-on Ampakine compounds. Overall operating expenses for the Company, excluding the non-cash charges, are expected to decline during 2007 compared to the prior year given that the expenses incurred for CX717 toxicology studies during 2006 are not anticipated to recur. Cortex’s cash and marketable securities amounted to $11,060,000 at March 31, 2007, and included net proceeds of approximately $5,100,000 from a registered direct offering of the Company’s common stock and warrants in January 2007. Spending during the quarter ended March 31, 2007 reflected a significant paydown of amounts accrued as of December 31, 2006, including amounts for the additional studies to define the toxicological findings for CX717. Cortex anticipates that its existing cash and marketable securities will support its funding requirements into 2008. During the quarter ended March 31, 2007, Cortex worked towards finalizing an extensive toxicology data package that as previously announced, was provided to the FDA in April 2007. Cortex believes that the submitted package provides data that demonstrates that the specific histopathological changes seen in animal toxicology studies, which previously caused the FDA to put CX717 on clinical hold, represent a postmortem fixation artifact that is not found in the tissue of the animal while it is living. While the clinical hold was lifted in October 2006, the Company continues to cooperate fully with the FDA and the decision whether to approve higher dose levels for CX717 in adults with Attention Deficit Hyperactivity Disorder will be made by the agency. Cortex Pharmaceuticals, Inc. Forward-Looking Statement (tables follow)
Contacts: Roger G. Stoll, Ph.D. Erika Moran/Dian Griesel, Ph.D. |