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Medical Technology Platform
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The following outlines information relevant to the development
pipeline for our various
Medical Technologies. For a more general overview
of our medical capabilities, please
click here.
General Overview
Our aim is to serve the concerns of both consumers and the industry alike.
As such, it is our goal
is to produce products and services that will better serve, as a
whole and in a highly productive and positive manner, both the
biotechnology industry and the general health needs of the human
race.
The discovery and development of our various
medical technologies is something that was
inevitable with both the ongoing deciphering of the human genome and
the general investigations into the use of
nutritional supplements.
And, nonetheless,
pharmaceutical products and many other biotechnologies will still
have important roles to play – especially in cases of certain
emergency situations and certain surgical procedures as well as for
severe cases where an 'extra edge' is required – and many great new
advances in
pharmaceuticals and many other types of biotechnologies will be able to evolve from our new
breakthrough understandings, thus resulting in even more major benefits for both consumer and producer
alike.
It is important to note that our discoveries can actually be incorporated
into the main research and development processes involved with just
about any other type of medical science so as to greatly refine and
enhance these processes for much faster, more reliable and more
highly defined results.
In fact, with ongoing research and development it is highly
envisaged that numerous highly extensive breakthroughs and general
developments will eventuate relative to many varied industry
sectors, including very specific industry sectors and application
areas that are currently under-established and/or underutilised.
Having said all of this, it is also important to note that
our medical technologies relate directly to both known and accepted fields of
science as well as newly evolving fields of expertise that are in their
infancy.
Intellectual Property Protection
At present no patents or provisional applications have been filed.
However, all patent protectable intellectual property is owned solely by
BC Biogenics Pty Ltd.
It is important to be fully aware that, due to the enormity and complexity of
our medical technologies and their numerous applications, there
are already and will continue to be many patents to be filed.
Having said this, please do consider the fact that
this simply helps to show just how much there is to gain by
being involved with any of
our medical technologies…!
Furthermore, before any patents can be filed there is still some primary 'ground work' that needs to be
conducted so as to establish a strong IP position that
will not come undone or be threatened in any way by patent
oppositions and the like.
It is also important to note that we have conducted extensive research in the quest to
develop what we have established and in this process we have not been
able to find any patents or publications that give definitive details to the same
extent or matching of what we have established.
Overview Of The Opportunity
Initially and most predominantly we are seeking to continue completing the
primary ground work that is required to secure a very strong IP
position. This will mostly entail completing the full mapping of
our newly discovered metabolic networks.
We will then be looking to fully apply to our
metabolic amplification platform technology not only
our newly discovered metabolic networks but also the
interrelated new understandings of metabolism and our new delivery
system.
It is important to note that the underpinnings of our
metabolic amplification platform technology will foster an explosion of new
and highly focused research and development that will, in turn, also
foster an explosion of both new and more highly evolved knowledge
and capabilities in
most all fields of medical science and biotechnology in general.
Our new breakthrough discoveries and understandings are truly going to change the face of both
the
nutritional supplements industry and the medical industry as a whole!
Utilising our overall new
knowledge, not only can we now make
nutritional supplements work
just as good as, and in many instances even better than, that of
pharmaceutical substances but long term ongoing treatment after the relevant conditions
have been rectified can result in biological and genetic changes
which protect against medical conditions reoccurring as well as from
related new conditions occurring.
Furthermore to this, the
treatments and general product concepts we are developing can also be utilised as straight forward
nutritional supplement products which will serve to prevent medical
conditions from occurring in the first place or, at least,
dramatically reducing the incidence rates of severe illness, which,
in turn, will still be treated with additional products/services
and/or simply higher dosage rates as required.
These factors should result in quite substantial and ongoing sales
volumes, even if people are not getting as sick and as often as
current trends are denoting.
This is especially true considering that the incidence rates for
most all illnesses are on the increase signifying that most all
people are not willing to make the necessary lifestyle changes that
are required for good health through healthy eating and other
healthy lifestyle traits but also because of the global growth rate
of the use and acceptance of
nutritional supplements for all matters of health.
And, having said all of this, our already established vast array of findings and developments
coupled with continuous ongoing research and development will surely
help to ensure that BC Biogenics Pty Ltd and any industry partners
that eventuate remain at the forefront of this new technological era
and thus also be able to maintain a commercial dominion over it for
many decades to come.
Something you truly need to understand is that the core of
our medical technologies permeates most all of the human genome – as discussed
here in the section on We Are But Mere Computer-Like Biological
Machines.
As such, what we are talking about here is not some mere
single or simple technology that fills 1 or maybe even 2 or 3 niche industry needs but
instead a whole new understanding of the human body that will have
numerous impacts on most all of the life sciences industry.
Our breakthroughs have the potential to be very
far reaching, especially with the current global growth rate of the
nutraceutical,
phytoceutical and
zooceutical markets and the consumer desire for such to be properly incorporated into
common everyday medicinal and general health therapies,
whether it be in replacement of such or complementary to such.
Lastly, it is also important to note that both the time frames and
the costs associated with fully developing all
treatments to commercial rollout (as well as that of many of the other new
technologies that will evolve) should be substantially reduced due
to our new knowledge of how to both inhibit/minimise side effects as
well as how to actually develop products and services based on
specific programmed and programmable genetic attributes.
Approximated Costs
Primary:
Patent and general IP strategy development: $20-30,000
National & international filing of primary platform patents: $2,500,000
Secondary:
Further strategy development and implementation: $40-60,000
Implementation of initial licensing and/or joint venture strategies: $150,000
We are also open to funding from
industry partners and others who would like to
establish full scale operations in relation to any of the various
applications of
our medical technologies .
As such,
industry partners and others are being
sought in order to further research the new pathway systems and to
produce various patent protectable viable commercial outcomes,
examples of which include:
- Novel and more highly advanced models of disease which
far more accurately predict human molecular processes and disease
pathologies
- Novel and more highly advanced, defined and accurate early
predictors of human ADME/tox
- Novel and more highly advanced, defined and accurate in
vitro tissue-mimicking toxicology assays
- Novel and more highly advanced, defined and accurate
computational models of in vitro and clinical trial response
- Novel and more highly advanced methods of improving substance stability, cell
permeability and tissue targeting
- Novel and more highly advanced methods of systems biology/multi-marker patterns
and
protein/antibody arrays
- Novel and more highly advanced antibody discovery and antibody
enhancement platforms and with the ability to determine antibody alternatives with superior
properties
- Novel and more highly advanced protein and gene expression manipulation
and amplification (programming) platforms – for both advanced and
novel medical treatment methods as well as for general biological
enhancement purposes
- Novel and more highly advanced substance and treatment discovery
platforms with the ability to determine a vast array of new candidates
and/or new applications
- Novel discovery platforms for highly
effective
nutraceutical,
phytoceutical and
zooceutical based therapies
- Novel platforms for combination therapies
- Novel and more highly advanced diagnostic procedures,
models, test kits, metabolic profiling and metabolic paneling –
including in relation to genetic testing
Most importantly, all of this also includes major breakthroughs in
understanding why in vitro studies and animal models do not
translate well into human evaluations and trials as well as how to
resolve many of these underlying issues.
With such as vast array of applications, it is both plain to see and extremely important to note that
our breakthrough new discoveries and understandings will not only become the new primary
underlying basis for just about all other platforms (and many other biotechnologies
in general) but will also become
the primary assessment tool for just about any other future biotechnology related
developments before any such investigations are to proceed past the
initial concept stage.
Due to the enormity of the project as a whole various consultants we
have sought advice from have advised that the platform technology is
best suited for licensing and/or joint ventures and/or other similar
arrangements with well established companies that have the appropriate
and relevant resources for each of their specific industry sectors
at their ready disposal.
As such, we also require a person, firm or group of firms that can
help us breakup the core of the overall project into its specific
applications for each of the numerous industry sectors it can be
applied to and then seek to license and/or negotiate joint ventures
and/or
whatever other kind of appropriate arrangements with appropriate
companies and other commercial avenues relative to each industry sector.
Having said all of this, potential means are being explored in order
to procure the people and/or organisations and/or other potential
means that are properly suited
to provide the assistance that we require.
However, if the quite large sums of money that will be required to
either partially or fully develop and commercialise some or all arms
of the project as a whole are solely achievable then we will alter
our activities to fully develop and commercialise those aspects of
the project entirely in-house.
It is for these reasons, and the fact that the underpinnings of
our medical technologies can be utilised in so many different
sectors of the industry, that we are very open to
partnering with well positioned and suited companies that compliment
our medical technologies.
Further Discussion & Negotiation
We are actively seeking both
industry partners and others to help us
further develop and commercialise the numerous technological
applications of our breakthrough medical capabilities.
If you would be interested in exploring our project further in relation to any
potential consultancy, partnering or other commercial arrangements with us,
documentation outlining the technological intellectual property in
question can be provided upon the signing of a confidentiality
agreement.
This documentation includes things such as: a full overview of the
new understandings and how the primary platform works as a whole;
examples of newly discovered pathway networks and how they interact
both with each other and with already known networks; examples of
therapeutic end products and their novel methods of application –
including examples of case studies we have conducted; examples of
novel methods of cell receptor targeting and cell receptor
manipulation; example substance assessments showing new insight into
their true metabolic nature; and much more. As such, all of this
will serve to give you a thorough understanding of this executive
summary.
If you would like to discuss a partnering or other opportunity
with us please feel free to
contact us.
For more general information about partnering with us and licensing
any of our
technologies, please
click here. |
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