Published: June 04, 2010
BioMimetic Therapeutics, Inc. to Present at the Noble Financial Equity Conference
FRANKLIN, Tenn. - (BUSINESS WIRE) - BioMimetic Therapeutics, Inc. (NASDAQ: BMTI) announced today that Larry
Bullock, CFO, will provide an update of corporate activities at the
Sixth Annual Noble Financial Equity Conference on Tuesday, June 8th
at 9:00 a.m. EDT. The presentation will be held in Room 3 - Piquet of
the Hard Rock Casino and Resort in Ft. Lauderdale, Fla.
A live audio webcast of the presentation will be available at http://noble.mediasite.com/mediasite/viewer/?peid=4ed1993dccff4f91ac70531ba8049db7
and on the Company's website at www.biomimetics.com.
The webcast will be accessible for a period of at least 30 days.
About BioMimetic Therapeutics
BioMimetic Therapeutics is a biotechnology company utilizing purified
recombinant human platelet-derived growth factor (rhPDGF-BB) in
combination with tissue specific matrices as its primary technology
platform for promotion of tissue healing and regeneration. rhPDGF-BB is
a synthetic form of one of the body's principal agents to stimulate and
direct healing and regeneration. The mechanism of action of this
platform technology suggests it may be effective in a broad array of
musculoskeletal applications, including the repair of bone, ligament,
tendon and cartilage. Through the commercialization of this technology,
BioMimetic seeks to become the leading company in the field of
orthopedic regenerative medicine. In 2005, BioMimetic received marketing
approval from the FDA for its first product, GEM 21S, as a
grafting material for bone and periodontal regeneration. Additionally,
BioMimetic Therapeutics has completed and ongoing clinical trials with
its product candidates Augment Bone Graft and Augment Injectable Bone
Graft in multiple orthopedic bone healing indications including the
treatment of foot and ankle fusions and the stimulation of healing of
fractures of the wrist. In November 2009, BioMimetic received approval
from Health Canada to begin marketing Augment as an alternative to the
use of autograft in foot and ankle fusion indications in Canada. In
February 2010, the Company submitted its Pre-Marketing Approval (PMA)
application to the FDA for the approval of Augment Bone Graft.
GEM 21S is a trademark of Luitpold Pharmaceuticals, Inc., who now
owns this dental related product and markets it through its Osteohealth
Company in the United States and Canada.
For further information, visit www.biomimetics.com
or contact Kearstin Patterson, corporate communications, at 615-236-4419.
BioMimetic Therapeutics, Inc.
Kearstin Patterson, Corporate
Communications
615-236-4419 (office)
615-517-6112 (mobile)
kpatterson@biomimetics.com
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