Biologix Hair Inc. (OTCBB:BLGX) (OTCQB:BLGX) has appointed Dr.
Guillermo A. Duran as Chief Medical Officer. Dr. Duran discovered
Follicle Nutrient Deficiency Syndrome (FNDS) to be the causal
effect of alopecia and went on to develop the preventive and
regenerative treatment now known as the Biologix Hair Therapy
System(TM).
Between mid-2004 and late 2011, more than 30,000
pre-clinical-trial treatments of Biologix Revive were administered
to 5,000-plus patients by a select private consortium of medical
clinicians located in South America. Participating patients either
suffered with varying degrees of FNDS or were seeking preventive
treatment to avoid onset of FNDS.
During those eight years, the clinicians subjectively estimated
that healthy hair growth has been maintained in virtually 100% of
those whose goal was to prevent the onset of Follicle Nutrient
Deficiency Syndrome (FNDS) and resulting alopecia.
The clinicians further estimate that between 80 - 85% of their
male patients and upwards of 90% of their female patients being
treated for FNDS and seeking hair regeneration therapy have been
able to regrow their lost hair.
Of the alopecia areata patients - both men and women - the rate
of success has been observed to be nearly 100%.
Dr. Guillermo Duran is a medical doctor practicing in
Barranquilla, Colombia. He graduated in 1988 from Juan N. Corpas
University's medical school in Bogota and completed specialization
in mesotherapy in 2000 at the Universite Victor Segalen Bordeaux 2
in France. Between 1994 and 2012 Dr. Duran continued his study of
mesotherapy and esthetic medicine in Brazil.
From 1989 to 1990 Dr. Duran served as Executive Director of San
Roque Hospital, as an Intensive Care Unit physician at the Ramon
Gonzalez Valencia Hospital in Bucaramanga from 1991-92. He has been
in private practice in mesotherapy and esthetic medicine since
1993. Dr. Guillermo Duran has been a guest speaker on the topic of
trichology at several conferences, including in Brazil in 2008,
Spain in 2011, and three times in Colombia from 2008-10.
Ron Holland, CEO of Biologix Hair Inc., commented, "I commend
Dr. Guillermo Duran for his professionalism and high scientific and
research standards. His discovery of FNDS and resultant formulation
of what has become Biologix Revive promises to be a significant
contribution to science and a benefit to millions of people around
the world, if and when regulatory approval is granted. As we
continue to take the necessary steps to prepare for application for
regulatory agency approval, Dr. Duran's direct assistance as Chief
Medical Officer will be especially helpful during this
process."
About Biologix Hair Inc. and Biologix Hair Science Ltd.
Biologix Hair Inc. (Biologix Hair), together with its wholly
owned biotechnology subsidiary, Biologix Hair Science Ltd. (TM)
(BHS), is focused on realizing the full market potential for its
patent-pending hair loss formula - Biologix Revive - and its
demonstrated ability to prevent and reverse the effects of
alopecia, which plagues hundreds of millions worldwide.
Between mid-2004 and mid-2012, more than 30,000
pre-clinical-trial treatments of Biologix Revive were administered
to 5,000-plus patients in South America suffering with varying
degrees of alopecia, as well as people seeking preventive
treatment. The participating treatment clinicians subjectively
observed and reported that virtually 100% of preventive care
clients continued to retain their healthy hair and an estimated
80-85% of the males and 90-plus% of the females treated for hair
regeneration experienced significant regrowth of their own natural
hair. And among alopecia areata patients, virtually total hair
regrowth was observed in 100% of the cases. To date, no negative
side effects have been reported.
BHS is currently focused on obtaining FDA approval for its
breakthrough hair loss prevention and regeneration therapy and has
initiated a research and development program with one of the
world's leading medical research universities, the Beijing
Institute of Technology (BIT). The R&D program, expected to
take approximately twelve months to complete, is an important final
step before formal clinical trials and the FDA approval process
begins.
Additionally, on May 11, 2012, Venable LLC, the Washington-based
law firm overseeing the worldwide IP and regulatory approval
processes on behalf of BHS, filed a Patent Cooperation Treaty (PCT)
application on behalf of BHS for Biologix Revive in Geneva,
Switzerland. The PCT is an international treaty, administered by
the World Intellectual Property Organization (WIPO), to which 144
countries have as of now contracted, including Canada and the
United States.
Biologix management is determined to be in a ready position to
capitalize on the high-margin sales potential of the Biologix Hair
Therapy System(TM), if and when FDA and other major market
approvals are forthcoming.
As BHS advances the regulatory approval process, Biologix Hair,
together with wholly owned subsidiary companies operated by BHS,
are rapidly developing a global distribution network of licensed
clinicians and medical practitioners seeking to become Certified
Biologix Hair Therapists(TM) and secure exclusive territorial
purchasing and treatment rights for the Biologix Hair Therapy
System(TM).
Biologix Hair has decided not to risk creating any potential
regulatory conflicts by offering treatment outside the United
States and other major high-product-margin markets until FDA
approval has been granted. Therefore, the Biologix Hair Therapy
System(TM) is not yet available other than to the 5,000+ patients
who participated in the pre-clinical-trials conducted in South
America.
To learn more about Clinician Licensing opportunities, Click
Here or call toll free +1 855.737.0333 or +1 647.344.5900.
Disclaimer
This announcement is not an offer to sell any Biologix Hair Inc.
("Biologix") securities. Offers for any given security are made
only through applicable offering circulars and related documents
filed with the SEC pursuant to the Securities Act of 1933 or the
Securities Exchange Act of 1934. Certain statements contained
herein and subsequent oral statements made by and on behalf of
Biologix may contain "forward-looking statements". Such
forward-looking statements are identified by words such as
"intends," "anticipates," "believes," "expects" and "hopes" and
includes, without limitation, the development of treatment centers
and approval from regulatory authorities. Forward-looking
statements express our expectations or predictions of future events
or results. They are not guarantees and are subject to many risks
and uncertainties. There are a number of factors beyond our control
that could cause actual events or results to be significantly
different from those described in the forward-looking statements.
Any or all of our forward-looking statements in this report or in
any other public statements we make may turn out to be wrong. We
undertake no obligation to publicly update or review any
forward-looking statements, whether as a result of new information,
future developments or otherwise. In Canada, Europe and the United
States, the Biologix treatment is not approved for use by Health
Canada, EMA or the FDA. The company makes no representations that
it will receive Health Canada, EMA or FDA approvals.
To view the images associated with this press release, please
visit the following link:
http://media3.marketwire.com/docs/n319blgA.pdf
Contacts: Biologix Hair Inc. Corporate Communications Toll Free:
+1 855.292.8585 OR +1
902.801.7920CorporateCommunications@BiologixHair.com
www.BiologixHair.com
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