Miravant Medical Technologies Chief Executive Officer Resigns; Board Names New Chairman and Executive Committee
08 Juillet 2005 - 3:00PM
Business Wire
Miravant Medical Technologies (OTCBB:MRVT), a pharmaceutical
development company specializing in PhotoPoint(R) photodynamic
therapy (PDT), announced today that its board of directors has
accepted the resignation of Gary S. Kledzik, Ph.D., as chief
executive officer (CEO), chairman and director. The Company's board
of directors named director Robert J. Sutcliffe as Miravant's new,
non-executive chairman, and announced the appointment of an interim
executive committee consisting of Robert J. Sutcliffe and director
Rani Aliahmad to coordinate management functions, identify CEO
candidates and recommend initiatives to increase productivity and
leverage Miravant's development programs. Miravant President David
Mai and CFO John Philpott will report to the interim executive
committee. Mr. Sutcliffe is a venture lawyer and business advisor
based in Los Angeles, where he is managing director of Craftsman
Capital Advisors LLC. Mr. Aliahmad serves as president of USA Call,
a provider of end-to-end mobile solutions and services for the
marketing arena. He has held several posts, including co-founder
and COO of Cardionomics and co-founder of Embryonix. "The board
thanks Dr. Kledzik, a Miravant founder, for his many years of
service and dedication to the Company," stated Robert J. Sutcliffe.
"Looking forward, the board intends to focus the company's efforts
on Miravant's pending PHOTREX(TM) clinical trials and deriving
shareholder value from our promising drug portfolio." Miravant
expects to commence this summer a confirmatory Phase III clinical
trial of its lead drug, Photrex(TM), an investigational treatment
for wet age-related macular degeneration (AMD). The U.S. Food and
Drug Administration (FDA) granted an approvable status to
Photrex(TM) in September 2004, which included a request for the
confirmatory clinical trial. The new clinical protocol was reviewed
by FDA under a Special Protocol Assessment, and the trial will be
initiated in the United Kingdom, Central and Eastern Europe. Wet
AMD is a debilitating eye disease that is the leading cause of
blindness in older adults. In addition to Mr. Aliahmad and Mr.
Sutcliffe, continuing directors re-elected to serve on the board of
directors at Miravant's annual shareholders meeting on June 23,
2005 included: Nuno Brandolini, Michael Khoury, David Mai, and
Kevin R. McCarthy. About Miravant Miravant Medical Technologies
specializes in PhotoPoint(R) photodynamic therapy (PDT), developing
light-activated drugs to selectively target diseased cells and
blood vessels. Miravant's primary areas of focus are ophthalmology
and cardiovascular disease with new drugs in clinical and
preclinical development. PHOTREX(TM) (rostaporfin), the Company's
most advanced drug, has received an FDA Approvable Letter as a
treatment for wet age-related macular degeneration and a Special
Protocol Assessment for a Phase III confirmatory clinical trial.
Miravant's cardiovascular development program, supported in part by
an investment from Guidant Corporation, focuses on life-threatening
coronary artery diseases, with PhotoPoint MV0633 in advanced
preclinical testing for atherosclerosis, vulnerable plaque and
restenosis. For more information, please visit our web site at:
www.miravant.com. Safe Harbor Statement under the Private
Securities Litigation Reform Act of 1995 The statements contained
in this press release that are not purely historical are
forward-looking statements within the meaning of Section 21E of the
Securities and Exchange Act of 1934, as amended, including but not
limited to those by Mr. Sutcliffe, and other statements about
improving the Company's performance, optimizing the Company's
business plan, the value and promise of its drug portfolio,
increasing productivity and leveraging its development programs,
the timing and commencement of the confirmatory Phase III clinical
trial in Europe; and development programs for in ophthalmology and
cardiovascular disease are forward-looking and relate to our future
plans, objectives, expectations and intentions. Our actual results
may differ materially from those described in these statements. For
instance, the occurrence of one or more of the following may cause
our results to differ from our plans: our operating capital may not
be sufficient to continue some or all of our development programs,
complete the PHOTREX Phase III clinical trial, complete the NDA
review process or continue as a going concern; we may not meet the
covenants of the December 2002 Debt Agreement, the August 2003
Convertible Debt and Warrant Purchase Agreement, or the March 2005
Note and Warrant Purchase Agreement, which would give the holders
under these agreements the right to call outstanding debt
immediately due and payable; we may not achieve certain milestones
required to receive future investments under our Collaboration
Agreement with Guidant Corporation; we may be unable to resolve all
issues or contingencies associated with the NDA; the FDA may
require further clinical or non-clinical studies before granting
PHOTREX marketing approval, or may limit labeling claims, or may
not grant marketing approval at all; even if approved, we may not
have the necessary resources or corporate partnering
relationship(s) to commercialize PHOTREX and its degree of
acceptance cannot be guaranteed; we may decide not to or may be
unable to continue the Company's current development programs; we
may not be able to demonstrate the safety or efficacy of our drugs
in development or achieve their regulatory approvals; and/or
partnering discussions may not progress or may not provide the
funding and support the Company needs. For a discussion of
additional important risk factors that may cause our results to
differ from those described above, please refer to our annual
report on Form 10-K for the year ended December 31, 2004 and other
quarterly and periodic reports filed with the Securities and
Exchange Commission. Our products require regulatory approval
before marketing, sales or clinical use. PhotoPoint(R) is a
registered trademark of Miravant Medical Technologies. PHOTREX(TM)
is a trademark of Miravant Medical Technologies.
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