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ADVENTRX Pharmaceuticals Reports Third Quarter 2007 Financial Results

     Conference call scheduled for November 13 at 1:30 p.m. (Pacific);
              simultaneous webcast at http://www.adventrx.com

    SAN DIEGO, Nov. 7 /PRNewswire-FirstCall/ -- ADVENTRX Pharmaceuticals,
Inc. (Amex: ANX), a biopharmaceutical research and development company
focused on commercializing proprietary product candidates for the treatment
of cancer and infectious diseases, today announced financial results for
the three-month and nine-month periods ended September 30, 2007.
    "We remain optimistic about our anticipated progress for the rest of
this year and into 2008, despite the recent setback in our CoFactor program
and our decision to discontinue enrolling patients in our Phase 3 study of
CoFactor for the first-line treatment of metastatic colorectal cancer,"
stated Evan M. Levine, chief executive officer of ADVENTRX. "We are
encouraged by continued progress with our vinorelbine emulsion product
candidate ANX-530 and our docetaxel emulsion product candidate ANX-514. We
expect that our emulsion product candidates will require less expenditures
and development time than CoFactor in pursuing regulatory approval for
marketing these product candidates."
    Three Months Ended September 30, 2007 Operating Results
    ADVENTRX's net loss was $5.9 million, or $0.07 per share, for the
three-month period ended September 30, 2007, compared to a net loss of $5.1
million, or $0.07 per share, for the same period in 2006. Included in the
loss for the three-month period ended September 30, 2007 was non-cash,
share-based compensation expense amounting to $689,000, compared to
$656,000 for the same period a year ago.
    Research and development, or R&D, expenses increased by $1.2 million,
or 37%, to $4.4 million for the three-month period ended September 30, 2007
from $3.2 million for the same period a year ago. The increase in R&D
expenses was primarily due to an $835,000 increase in expenses related to
research-related manufacturing and quality assurance activities for our
product candidates and a $347,000 increase in personnel and related costs.
R&D expenses for the three-month period ended September 30, 2007 included
non-cash, share-based compensation expense amounting to $290,000, compared
to $110,000 for the same period a year ago.
    Selling, general and administrative, or SG&A, expenses decreased
slightly by $76,000, or 4%, to $2.0 million for the three-month period
ended September 30, 2007 from $2.1 million for the same period a year ago.
The decrease in SG&A expenses was substantially due to a $120,000 decrease
in business development expense and a $147,000 decrease in share-based
compensation expense, partially offset by a $164,000 increase in legal fees
primarily related to patent applications. SG&A expenses for the three-month
period ended September 30, 2007 included non-cash, share-based compensation
expense amounting to $399,000, compared to $546,000 for the same period a
year ago.
    Interest income amounted to $532,000 for the three-month period ended
September 30, 2007, compared to $221,000 for the same period a year ago.
    Effective January 1, 2007, the Company adopted FASB Staff Position on
No. EITF 00-19-2, Accounting for Registration Payment Arrangements, or FSP
EITF 00-19-2. Pursuant to FSP EITF 00-19-2, the Company determined that no
contingent liability was required to be recognized as of September 30, 2007
relating to a class of warrants issued in July 2005 that contained a
registration payment arrangement, and accordingly, the carrying amount of
the warrant liability that had been reported in previous periods was
eliminated. In applying the new method retrospectively, the comparative
financial statements of prior periods have been adjusted to eliminate the
fair value of the warrant liability.
    Nine Months Ended September 30, 2007 Operating Results
    The net loss for the first nine months of 2007 was $16.8 million, or
$0.19 per share, compared to $24.3 million, or $0.34 per share, for the
same period a year ago. Included in the loss for the nine-month period
ended September 30, 2006 was a charge of $10.4 million of in-process
research and development expense recorded in connection with the
acquisition of SD Pharmaceuticals and eight of its product candidates.
    R&D expenses were $12.0 million for the first nine months of 2007,
compared to $8.9 million for the same period a year ago. The increase in
R&D expenses for 2007 was primarily related to a $1.4 million increase in
expenses related to research-related manufacturing and quality assurance
activities for our product candidates, a $214,000 increase in external
preclinical study fees and expenses mostly related to ANX-201 and a $1.3
million increase in personnel and related costs.
    SG&A expenses were $6.8 million for the first nine months of 2007,
compared to $5.5 million for the same period a year ago. The increase in
SG&A expenses for 2007 was substantially due to a $1.1 million increase in
SG&A personnel and related costs and a $251,000 increase in legal fees
primarily related to patent applications.
    Revenue of $500,000 in the first nine months of 2007 represented a
license fee earned from licensing ANX-211, compared to no revenue for the
comparable period in 2006.
    Balance Sheet Highlights
    As of September 30, 2007, the Company had cash, cash equivalents and
investments in securities totaling $38.6 million, including cash and cash
equivalents of $19.3 million and short-term investments in securities of
$19.3 million. Stockholders' equity amounted to $35.9 million as of
September 30, 2007.
    Conference Call and Webcast
    Management will host a conference call with a simultaneous webcast that
will take place on Tuesday, November 13 at 1:30 P.M. Pacific/4:30 P.M.
Eastern to discuss the third quarter of 2007 and provide an update on its
clinical trials and any available data. Evan M. Levine, Chief Executive
Officer, and Gregory P. Hanson, Senior Vice President and Chief Financial
Officer, are scheduled to lead the call and will be joined by other members
of the Company's senior management team. The webcast will be available live
via the Internet by accessing ADVENTRX's web site at
http://www.adventrx.com under "Investors" or by telephone at (888) 812-8595
(domestic) or (913) 312-6699 (international). Replays of the webcast will
be available for 30 days, and a phone replay will be available through
December 13, 2007 by dialing 888-203-1112 and entering the passcode
1410376.
    About ADVENTRX Pharmaceuticals
    ADVENTRX Pharmaceuticals is a biopharmaceutical research and
development company focused on commercializing proprietary product
candidates for the treatment of cancer and infectious diseases. The Company
seeks to improve the performance and safety of existing treatments by
addressing significant problems, such as drug metabolism and
bioavailability, excessive toxicity and treatment resistance. More
information can be found on ADVENTRX's web site at http://www.adventrx.com.
    Forward Looking Statements
    ADVENTRX cautions you that statements included in this press release
that are not a description of historical facts are forward-looking
statements that involve risks and assumptions that, if they materialize or
do not prove to be accurate, could cause ADVENTRX's results to differ
materially from historical results or those expressed or implied by such
forward-looking statements. These risks and uncertainties include, but are
not limited to: the risk that ADVENTRX will be unable to raise sufficient
capital to fund the projects necessary to meet its anticipated or stated
goals and milestones; the ability to timely enroll subjects in ADVENTRX's
current and anticipated clinical trials; the timing and success of clinical
trials; the potential for ADVENTRX's product candidates to receive
regulatory approval for one or more indications on a timely basis or at
all; the uncertain process of seeking regulatory approval; other
difficulties or delays in developing, testing, manufacturing and marketing
ADVENTRX's product candidates; the potential for regulatory authorities to
require additional preclinical work or other clinical requirements to
support regulatory filings; the scope and validity of patent protection for
ADVENTRX's product candidates; adverse side effects or inadequate
therapeutic efficacy of ADVENTRX's product candidates; the risk that
preclinical results are not indicative of the success of subsequent
clinical trials and that products will not perform as preclinical and
clinical data suggest or as otherwise anticipated; and other risks and
uncertainties more fully described in ADVENTRX's press releases and
periodic filings with the Securities and Exchange Commission. ADVENTRX's
public filings with the Securities and Exchange Commission are available at
http://www.sec.gov. You are cautioned not to place undue reliance on these
forward-looking statements, which speak only as of the date when made.
ADVENTRX does not intend to update any forward-looking statement set forth
in this press release to reflect events or circumstances arising after the
date on which it was made.
                              [Tables to Follow]



               ADVENTRX Pharmaceuticals, Inc. and Subsidiaries
                       (A Development Stage Enterprise)
             Summary Condensed Consolidated Financial Information
                     (In 000s except for per share data)

    Consolidated Statement of    Three Months Ended      Nine Months Ended
     Operations Data:               September 30,           September 30,
                                  2007        2006        2007        2006
                               (Unaudited) (Unaudited) (Unaudited) (Unaudited)

    Revenues                         $.          $.         $500         $.

    Operating expenses:
      Research and development    4,422       3,224       12,047      8,941
      Selling, general and
       administrative             1,979       2,055        6,794      5,545
      Depreciation and
       amortization                  45          49          150        128
      In-process research
       and development                .           .            .     10,422
        Total operating
         expenses                 6,446       5,328       18,991     25,036
    Loss from operations         (6,446)     (5,328)     (18,491)   (25,036)

      Interest income               532         221        1,730        710
    Loss before income taxes     (5,914)     (5,107)     (16,761)   (24,326)

      Provision for income
       taxes                          .           .            .          .
    Net loss                    $(5,914)    $(5,107)    $(16,761)  $(24,326)

    Net loss per share -
     basic and diluted           $(0.07)     $(0.07)      $(0.19)    $(0.34)

    Weighted average shares -
     basic and diluted           90,008      73,436       89,798     70,896



    Balance Sheet Data:
                                                 September 30,    December 31,
                                                     2007             2006
                                                 (Unaudited)

    Total cash and investments in securities       $38,614          $51,745
    Net working capital                             35,489           49,889
    Total assets                                    39,877           52,798
    Total liabilities                                3,977            2,484
    Stockholders' equity                            35,900           50,314


SOURCE ADVENTRX Pharmaceuticals, Inc.




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  • http://www.adventrx.com
    CONTACT:
    Investors, Ioana C. Hone of ADVENTRX
    Pharmaceuticals, Inc., +1-858-552-0866