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R & D Applications
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Our overall discoveries can also 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.
The following are some more examples of how the underpinnings of our
medical technologies can be utilised to
produce more effective, efficient and safer treatment outcomes.
Therapeutics Research & Development
Due to our overall discoveries and developments, not only can
currently existing treatments be substantially improved upon but
hundreds, if not thousands, of new therapeutic products can be developed
that target the same and/or similar systems as current treatments
but simply via new pathways, receptors and so on.
This also includes
the development of a number of companion and synergistic treatment
methods, utilising both new and existing substances, that can work
systematically to substantially enhance treatment outcomes.
Furthermore, all of this also means that:
- in many instances far lower dosages of
substances can be utilised yet with the same or better therapeutic
outcomes;
- where the diagnosed need is ascertained,
dosage rates can usually be increased substantially past currently
prescribed dosage rates without toxicity occurring;
- new candidate substances and formulas can
be assessed for usefulness and viability far more quickly and
effectively;
- many substances that have previously not
made it through to commercialisation and/or have not shown any
reasonable usefulness can readily be re-assessed to see if the whole
problem with them was simply that they were actually being
assimilated into conflicting pathways, receptor systems and so on;
- many substances can
be reformulated to make them better and/or usable for both known and
novel indications;
- many combination products can be developed
for both known and novel indications;
- many new genetic, biochemical and general
biological systems can now be defined and utilised to produce
numerous new and/or advanced therapeutics as well as many new and/or
advanced research and diagnostic
tools; and
- many genetic, biochemical and general
biological systems (and their related medical conditions) that are
currently very difficult to target, either for research or treatment
purposes, can either now or in the near future be readily targeted.
Initial testing of our new know how on a number of already existing
and approved substances (over 200 so far) has shown nothing short of
remarkable findings – including that of just how precise, effective
and extensive the overall underpinnings of our medical technologies
really are.
We have also conducted some minimal initial trials of some of these
substances in relation to conditions such as: rhinitis; asthma; insomnia; muscular joint problems; hives reactions; mental diseases
and general mood disorders; sinus and chest congestion; back
problems; drug addictions; general immuno support; libido and
fertility issues; inflammatory conditions; viral and bacterial
infections; and analgesia – all with profound effectiveness and
safety!
It should also be pointed out that we have also successfully
determined that our new technologies can also be utilised for use
with both topical and injectible applications in exactly the same
manner.
Novel & Advanced Platform Applications
It is important to note that the overall underpinnings of our
medical technologies 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 in
most all fields of medical science and biotechnology in general.
In fact, with ongoing research and development it is highly
envisaged that numerous extensive breakthroughs and general
developments will eventuate relative to many industry
sectors, including application
areas that are currently under-established and/or underutilised.
Having said all of this, it is important to note that the underpinnings of
our medical technologies can be utilised to further produce
various patent protectable commercial outcomes relative to:
- 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 (including that relative to
nanotechnologies)
- 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.
Cutting Costs & Lead Times
It is also very important to note that both the time frames and the
costs associated with fully developing all technologies and
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 the products and
services based on specific programmed and programmable metabolic
expression attributes.
Our breakthrough findings and developments will inevitably lead to
much faster and easier regulatory fulfilments and this will
inevitably also lead to much cheaper research and development cost,
thus resulting in much cheaper products and services for both the
industry and consumers alike.
For information regarding the development pipeline of this technology, please
click here. |
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