CFA IPO Spotlight: Tercica Inc Prospectus Information
  DOW JONES NEWSWIRES
  DJ CFA SOURCE:SEC S-1
  OFFERING: COMMON
  AMOUNT: Up to $86.25 million
  SEC RECEIVE: 09/12/2003
  SHELF FILING: N
  POST EFFECTIVE: N
  SELLING HOLDER: N
          WASHINGTON -- Tercica Inc. filed an initial public offering
  Friday with the Securities and Exchange Commission to sell up to $86.25
  million in common stock. This is a summary of its prospectus, as
  provided to the SEC:
  THE COMPANY
          Tercica, based in San Francisco, is a biopharmaceutical company
  focused on developing and commercializing recombinant human insulin-like
  growth factor-1, or rhIGF-1, for treating short stature, diabetes and other
  endocrine system disorders.
          Tercica licensed Genentech Inc.'s (DNA) rights to develop,
  manufacture and commercialize rhIGF-1 for a broad range of indications,
  including for short stature worldwide and for diabetes in the U.S.
          Tercica has Phase III clinical trial data for rhIGF-1 for its first
  short stature indication, severe pediatric IGFD. The company said it intends
  to submit a new drug application to the U.S. Food and Drug Administration by
  early 2005 after completing the transfer and validation of its rhIGF-1
  manufacturing process to its contract manufacturer.
  OFFERING INFORMATION
          Tercica plans to sell up to $86.25 million in common stock. Details
  about the price per share and number of shares offered weren't included in
  the filing.
          The company said net proceeds from the offering will be used for
  late-stage clinical trials of rhIGF-1, for launch and post-launch sales and
  marketing activities for rhIGF-1, for manufacturing transfer and validation
  of rhIGF-1, and for general purposes, including the possible
  acquisition of new products or product candidates.
          Morgan Stanley, Lehman Brothers and Pacific Growth Equities LLC were
  listed as underwriters for the offering.
          The company plans to list its common stock on the Nasdaq National
  Market under the symbol TRCA.
          The $86.25 million valuation was estimated solely for calculating the
  registration fee, the filing said. Often, the eventual price terms of an IPO
  differ substantially from the initial valuation.
  EARNINGS
  Six Months Ended June 30,
                                2003            2002
  =                           ----------      ----------
  Research and development   $6,153,000        $453,000
  Net income                ($7,742,000)    ($6,243,000)
  Figures in parentheses are losses.
  BUSINESS STRATEGY
          Tercica's goal is to capitalize on the opportunities presented by
  rhIGF-1 and to develop and commercialize additional new products for the
  treatment of endocrine disorders.
          To achieve this, Tercica plans to seek FDA approval of rhIGF-1 for
  severe pediatric IGFD, or IGF-1 deficient; expand its severe pediatric IGFD
  indication to all children with IGFD; develop rhIGF-1 for additional
  indications; establish a U.S. sales and marketing organization; and broaden
  its portfolio of endocrine-related products.
  RISK FACTORS
          Tercica said risk factors include being a development-stage company
  with a limited operating history; uncertain future profitability; the loss of
  licenses from Genentech; failure to get regulatory approvals; delays in
  transferring or validating the Genentech rhIGF-1 manufacturing process at its
  contract manufacturers; and failure to get FDA approval of the contract
  manufacturers' facilities, or those facilities becoming unavailable.
          Tercica said other factors include competition to develop and gain
  FDA approval of rhIGF-1; discoveries or developments of new technologies
  possibly making rhIGF-1 obsolete; rapid and significant technological change;
  inability to commercialize rhIGF-1; failure to protect intellectual property
  rights; rhIGF-1 failing to achieve market acceptance; and inability to
  establish a direct sales force in the U.S.
          Other factors include possible reliance on others to market and
  commercialize rhIGF-1 in international markets; failure to identify and
  in-license other products or product candidates; failure to get capital
  needed for operations; inability to manage expected growth; third-party
  clinical research organizations not performing in an acceptable and timely
  manner; product liability lawsuits; and ability to attract and keep
  additional qualified personnel.
  MANAGEMENT
  Name                           Age   Position
  =- -----                         ---   --------
  John A. Scarlett, M.D.          52   President, chief executive and
                                       director
  Alexander Barkas, Ph.D.         56   Chairman
  Scarlett has served as president and CEO and as a member of the board since
  February 2002.
  Barkas has served as chairman since August and as a member of the board since
  May 2002.
  SHAREHOLDERS
  Shareholder               Shares Before Offer (%)   After Offer
  =-----------               -----------------------   -----------
  MPM Capital L.P.              26,770,000 (36.8%)       N/A
  Prospect Management Co. II    13,050,000 (17.9%)       N/A
  Rho Ventures                   8,000,000 (11.0%)       N/A
  Genentech Inc.                 4,070,667  (5.6%)       N/A
  Care Capital LLC               4,000,000  (5.5%)       N/A
  MedImmune Ventures Inc.        4,000,000  (5.5%)       N/A
  FINANCIAL CONDITION AND LIQUIDITY
          Tercica has incurred net losses since inception, and as of June 30
  had an accumulated deficit of about $16.7 million.
          Through Aug. 31, the company had funded its operations and growth
  from inception with about $66.8 million in private equity financings, the
  filing said.
          Cash and cash equivalents decreased to $10.4 million at June 30 from
  $15.9 million at Dec. 31, 2002.
  -By Brian Coyle; Dow Jones Newswires; 202-862-3545 |