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October 29, 1998
CYPRESS BIOSCIENCE, INC. (NASDAQ: CYPB) "FDA Panel Recommends Approval of Prosorba Column for Moderate to Severe RA"
RESEARCH UPDATE REITERATE "BUY" RECOMMENDATION As anticipated in our report of October 14, 1998, an FDA Advisory Panel voted 10-to-1 today to recommend approval of CYPBs Prosorba Column for the treatment of rheumatoid arthritis ("RA"). The Panel recommended that the FDA approve the column for the treatment of patients with moderate to severe RA, that have failed second-line therapies, or DMARDs, such as methotrexate. The Company anticipates formal FDA approval by the end of this year. We are very encouraged that the recommendation included patients with moderate, in addition to severe, RA patients, as we believe this significantly increases the potential market for the Prosorba Column. The panels recommendation is conditional on CYPB conducting a post-marketing study of the Prosorba Column in conjunction with other second-line therapies, or in repeated therapy. We are not surprised by this development and, in fact, it is our understanding that CYPB had already submitted such a proposal to the FDA and planned to complete these additional studies anyway. CYPB has been preparing for this outcome, and is currently in process of hiring its internal salesforce. CYPB is planning to train its salesforce over the next couple of months, and commence a "rolling" product launch (concurrent with additional salesforce training) during the first quarter of 1999. With respect to marketing towards the medical community and leading rheumatologists, CYPB management has scheduled a number of mailings and speaking engagements, including the presentation of scientific papers at the upcoming American College of Rheumalologists (ACR) annual meeting in San Diego in mid-November. Additionally, CYPB is hosting satellite symposia at that conference (on November 12, 1998) entitled "Emerging Role of Apheresis with Protein A Immunoadsorption," which includes presentations by leading investigators of the Prosorba Column. Our basic research report on CYPB, dated October 14, 1998, is available on our website at www.SmallCapsOnline.com, and we recommend investors review this report for details on the Company, the Prosorba Column, the market for RA therapies and competition. We believe CYPB is undervalued based on Prosorba for RA alone, without regard for the significant potential of its Cyplex technology, and are reiterating our BUY recommendation for investors tolerant of risks associated with small-cap and micro-cap investments.
FOR ADDITIONAL INFORMATION Contact SmallCaps Online LLC 212-554-4158 For corporate inquiries: Jeffrey B. Davis For investor inquiries: Jennifer LaVin For media inquiries: Jeni Gray RISK CONSIDERATIONS This section of the document is to remind potential investors to undertake a prudent level of due diligence prior to making an investment in securities of Cypress Bioscience, Inc. For a complete description of risks and uncertainties to CYPBs business, see the Risk Factors section in CYPBs SEC filings, which can be accessed directly from the SEC Edgar filings at www.SEC.gov on the internet. Other potential risks include:
SOURCES FOR ADDITIONAL INFORMATION The following are website addresses offering related information, and links to other sources of information. www.CypressBio.com CYPBs corporate website www.SmallCapsOnline.com SmallCaps Onlines site for company information and research www.FDA.gov US Food and Drug Administration homepage www.rheumatology.org American College of Rheumatology homepage www.arthritis.org Arthritis Foundation homepage www.WHO.int World Health Organization homepage www.AABB.org American Association of Blood Banks homepage www.AMA-Assn.org American Medical Association homepage www.SEC.gov U.S. Securities and Exchange Commission, with links to EDGAR filings
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