MIV Therapeutics Announces Jesup & Lamont Maintains Buy Recommendation and Revises MIV Target Price to Reflect Reverse Split
2008-07-14 06:30:00
MIV Therapeutics Announces Jesup & Lamont Maintains Buy Recommendation and Revises MIV Target Price to Reflect Reverse Split
ATLANTA–(EMWNews)–MIV Therapeutics, Inc. (OTCBB:MIVI) (Frankfurt:MIV), a leading
developer of next-generation coatings and advanced drug-delivery systems
for cardiovascular stents and other implantable medical devices,
announced that senior research analyst Kenneth Siri, CFA, of Jesup &
Lamont Securities, maintained his Buy rating for MIV Therapeutics and
adjusted his target price to $20.00 to reflect the Company’s
recent 1-for-10 reverse stock split.
In a research note on July 8th, Jesup & Lamont
stated that the split is designed to improve the stock’s
marketability to institutional investors. As a result of the 1-for-10
reverse split, Siri is adjusting his price target from $2.00 per share
to $20.00 per share.
Jesup also notes that MIV has the potential to penetrate the
drug-eluting stent (DES) market by addressing DES safety concerns, while
maintaining efficacy and targeting additional lesions currently out of
reach of DES. Additionally, Siri believes that the company’s
drug delivery technology (hydroxyapatite or HAp), requires little
modification for orthopedic use, making MIV a prospective player in
orthopedic drug delivery.
Below is a link to the research note:
http://www.mivtherapeutics.com/_resources/articles/070808-Jesup-
Lamont.pdf (Due to its length, this URL may need to be
copied/pasted into your Internet browser’s address field. Remove
the extra space if one exists.)
About MIV Therapeutics
MIV Therapeutics is developing a next-generation line of advanced
biocompatible coatings for passive and drug-eluting applications on
cardiovascular stents, as well as for a broad range of other implantable
medical devices. The Company’s ultra-thin coating formulation is
designed to protect surrounding tissue from potentially harmful
interactions with bare metallic stents. This coating platform is derived
from hydroxyapatite (HAp), an organic material that has demonstrated
excellent in vivo safety and biocompatibility. Hydroxyapatite is
a porous material that makes up the bone mineral and matrix of teeth,
and is widely used today as a bone substitute material and for coatings
on implantable fixation devices in orthopedic, dental and other
applications. The Company’s novel polymer-free drug-eluting technologies
based on HAp could also provide an attractive alternative to current
polymer-based drug-eluting coatings on the stent market, which have been
associated with undesirable effects. The Company’s drug-eluting coatings
are additionally designed to suit a broad range of implantable medical
devices that could benefit from highly customizable drug release
profiles. MIV Therapeutics has a Collaborative Research Agreement with
the University of British Columbia and has received a government grant
for its research program on the “Development
of Novel Drug Eluting Composite Coatings for Cardiovascular Stents,”
under the National Research Council-Industrial Research Assistance
Program. Under this sponsorship, the Company is expected to complete its
drug-eluting research and development program and to reach product
commercialization. MIV’s intellectual property portfolio includes
patents held by the University of British Columbia and exclusively
licensed to MIV. Key patent applications filed simultaneously in various
countries around the world further protect the commercial exclusivity of
MIV’s inventions in the global marketplace. For more information, please
visit www.mivtherapeutics.com.
Forward-Looking Statements
Except for the historical information contained herein, the matters
discussed in this press release are forward-looking statements. All
statements that discuss expectations and projections with respect to
future matters including, without limitation, statements relating to the
safety and efficacy of the Company’s product
and the ability of the Company’s product to
rejuvenate the stent market are forward-looking statements. Such
statements are indicated by words or phrases such as “proposed,”
“expected,” “believe,”
“will,” “breakthrough,”
“significant,” “indicated,”
“feel,” “revolutionary,”
“should,” “ideal,”
“extremely” and “excited.”
Such statements include but are not limited to that the split is a
positive move and will result in an increase in attractiveness to
institutional investors. These statements are made under “Safe
Harbor” provisions of the Private Securities
Litigation Reform Act of 1995. Actual results may differ materially from
those described in forward-looking statements and are subject to risks
and uncertainties including, without limitation, market acceptance of
the Company’s product, the ability of the
Company to raise sufficient funding and to continue to develop its
various business interests as presently contemplated, and other factors
identified in the Company’s filings with the Securities and Exchange
Commission including, without limitation, the Company’s annual report on
Form 10-K for the year ended May 31, 2007 and Forms 10-Q. The Company
expressly disclaims any obligation to update publicly or otherwise
revise these statements, whether as a result of new information, future
events or otherwise, except to the extent required by law.
For Investor Inquiries: L. Huston x14 & Associates, Inc. Media Inquiries: Cassie Wallace, 781-684-0770 |
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