upon reflection, the reason for delays should be o
Post# of 9123
(Total Views: 704)
Posted On: 11/09/2018 4:51:27 AM
upon reflection, the reason for delays should be obvious to naysayers who seem determined to control the discussion no matter what i do- having spent thousands of hours on this board.
i dont think they even read my posts or perhaps those of other longs
all my life i've seen ppl captured in prisons of their own making- thought patterns resulting from millions of decisions they have made that they cant even remember,let alone take responsibility for,but rather always look for a scapegoat-and in that tunnel which they cannot see outside of they are trapped-and cant find the answers which come from outside that tunnel
e.g why arent those familiar with dr faro buying nnlx stock by the millions?
well, to start with how many ppl even know of faros involvement in a no info company called nnlx????? very very few
they cant know unless
1) they read these stock boards-so how many do that -very very few -my best friend who dragged me into pennies didnt even know these stock boards existed
how many invest in a no info co-very very few- thats an important part of the answer but when i detailed that as an important part of the answer many years ago here i was heavily attacked by longs
bc its no info the only place to find info is the website or these boards
2) or unless they were involved in the private closed meetings-very very few were involved in those secret meetings bc as always big co's selfishly want their involvement hidden until they have successfully cornered the market and as usual has an nda
3- even if they know how many even know how to trade penny stocks -very very few
even if they know nanologix name how are non-traders even going to find the ticker and set up a brokerage acct and trade -very very few will -laziness- ppl dont like to go outside their comfort zones
4) buying stock- no matter how much- will not raise one cent to fund the study- funded from both Federal Grants and a raise of investment capital-8-20-18
and those who were involved in the secret meetings could not buy stock bc that would be insider trading-can they now? i dont know -a matter of interpretation-have all the material info from those secret meetings been distilled by nnlx in updates to stockholders who have signed up for updates? -for our part we've posted all those updates here and the board info
1of the disadvantages of a no info stock is the high likelihood of insider trading-which is why i have purposefully had no personal contact w the company while its otc no info
now naysayers should understand this/the mindset of breaking through stubborn resistance to break into the market
we know nnlx has a superior product in the n assay and petriplates
but outsiders want to see it proved- show me-they all live in the show me state- thats what studies are for -
nobody wants to buy the product until years of specialized studies -ISNT THAT HOW BIOTECH WORKS!!!!
THEY ARENT GOING TO MAKE AN EXCEPTION FOR LITTLE OLD NNLX-
nnlx did years of studies internally and years of studies outside before much traction w their superior petri plates
going thru the same process now w the n assay!!!!!
every company wants everything handed to them on a silver platter -all the work including modifications for their company already done -the way of the selfish world-and if the big co's dont get their way in everything they would rather pout and out than play
thats the very difficult game these small startups have to play-many such startups have had better products-but very few startups succeed-this is NOT unique to nnlx as some pretend in the blame game
many of the frustrations posted by posters re nnlx apply to almost all penny stocks-
but ppl forget why they got into penny stocks- blue chips have their frustrations also -chiefly is that retail traders cant compete w the saturated insider trading/supercomputers and fraud that is involved in blue chips
its frustrating to the nnlx officers etc also, as year after year goes by without being able to monetize their time and efforts-pure logic!
Posted On: 10/26/2018 9:16:31 AM
Posted By: Fibonacci233
Nanologix Incorporated
New write up that will be posted on our new website soon for our patented diagnostic. Comments and interest welcomed:
Nanologix' N-Assay offers an innovative solutions to a major problem that has plagued physicians over the years.
In medicine, nothing gets a clinician's attention like sepsis. When one has seen a patient who had previously been doing just fine suddenly take a turn for the worse, management decisions must be made without hesitation. In the case of a septic patient, seconds mean the difference between life and death, and minutes are a luxury that neither the clinician nor the patient may afford. The post-operative patient, the post-partum patient, the ICU patient... any patient is at risk of encountering a virulent pathogen in the hospital, and without an astute clinician ready to respond, serious consequences will occur. It's not surprising that the Infectious Disease Society of America estimates just this year that treating infections cost 21 to 34 billion dollars annually, in the US alone.
Clinicians currently have two techniques at their disposal when treating a presumed infection -culture, and PCR. The traditional technique of culture is labor intensive, requires laboratory-trained personnel, and correctly obtained, viable material. Although this method is relatively inexpensive, it is incredibly time-consuming. Patients often find it hard to believe that obtaining a culture result and antibiotic sensitivity profile may take 5 days! While the clinician is waiting for the results, they are throwing everything they've got at the possible infection. This is truly an empiric approach, and here it pays to have an experienced clinician by your side.
The alternative method, PCR, is much faster, much more sensitive, but also much more expensive. This newer technique also costs a great deal more, and requires highly trained personnel to operate the devices. These machines also incur a large capital investment by the hospital, as well as annual maintenance. In spite of the strengths of PCR, it also has weaknesses -it is unable to differentiate the difference between live/dead bacteria, and can not provide estimates relating to the degree of the inoculum. This information is essential for the clinician in directing targeted therapy, so again, they are ultimately forced to rely on their experience when treating the patient.
Regardless of one's opinion as to whether culture or PCR is the better option, the data over the last few decades shows the depressing truth -neither option is offering us any real advantage. This is made clear when one looks at the development of antibiotic resistance. These bugs have continued to grow and evolve, and a few years ago, a gonorrhea "super-bug" was isolated -showing resistance to every antibiotic available. We are clearly losing the war against these single-cell enemies!
In answer to this major problem, we have developed and patented an approach that takes all of the advantages of both culture and PCR (specificity, sensitivity, speed, and accuracy as well as ease of use), and none of the disadvantages. This technique, termed the N-Assay, is an antibody-based assay that targets potentially any bacterial pathogen (and has also been seen to detect yeast), in as little as 30 minutes. In addition, when incubated for 6 hours, this test not only provides a bacterial identification, but also allows the clinician to determine which antibiotic will work in treating the infection. This test will dramatically shorten the amount of time required for a clinician to wait when treating the ill patient, and should ultimately save billions in healthcare spending. Furthermore, by more accurately targeting the right bacterium with the correct antibiotic, we should drastically reduce the incidence in antimicrobial resistance.
We have already used a pilot version of this test in detecting group B streptococcus colonization in pregnant women, and have won an award at an OB GYN conference when presenting our data. The clinicians see that this test has tremendous potential, and are eager for it to be available, as they simply need better methods to more accurate diagnose infection. With the right resources, we will be able to expand this test to additional bacterial pathogens, such as E. coli, Enterococcus, MRSA, and any other clinically relevant pathogen.
Posted On: 09/07/2018 10:21:03 AM
Posted By: LuckyDog111
Notice of Upcoming NanoLogix Website Revision
Request For Confirmation of Continuing Interest From Newsletter Subscribers
NanoLogix is pleased to announce the Company website will be extensively revised and updated during September and October. The Company requests that those Newsletter Subscribers who are interested in continuing to receive updates of NanoLogix news through our iContact news service to send a confirmation email to: info@nanologix.com
This revision will enable the Company to significantly improve the website, providing the ability to respond rapidly to business events and to quickly furnishbusiness, technology, and hospital study updates.
8-20-18
NanoLogix Attends Series of Meetings In Houston
Preparation for Pre-test Development Study
NanoLogix is pleased to announce their attendance at a series of meetings in Houston with Drs. Sebastian and Jonathan Faro and the CEO of a California-based Biotechnology firm. The purpose of the meetings was for coordinating forces for a research study for development of a rapid pre-test for use with the patented Nanologix N-Assay bacteria diagnostic. The meetings dealt with organization and staffing of a research study at two major Houston hospitals, funded from both Federal Grants and a raise of investment capital , and the specific personnel required for the successful execution of the study. The personnel agreeing to participate in the study are seven MDs, two research nurses, two microbiologists, at least two laboratory technicians, and the CEO of the California Biotechnology company. NanoLogix personnel and the CEO of the Biotechnology company have signed a mutual non-disclosure agreement limiting what can presently be revealed but once funding has been obtained and the study registered with the FDA and initiated, the identity of the pre-test development company should be available as public knowledge.
The purpose of the pre-test use with the N-Assay is to have a pre-test that will indicate the presence of a specific bacteria with minutes, for which the N-Assay can then be used to rapidly determine both the concentration of the bacteria and its sensitivity to various antibiotics, furnishing Point of Care (POC) personnel the ability to effectively treat the patient with the specific antibiotic required. This development will significantly reduce reliance upon broad-spectrum antibiotics, which contribute to the major worldwide problem of the development of antibiotic-resistance for many bacteria.
NanoLogix has also agreed to fund an existing laboratory in Houston currently in use as a clinical laboratory for the medical group associated with Dr Jonathan Faro. This lab will be crucial to the testing of patient samples during the upcoming study.
Dr. Jonathan Faro, PhD, MD stated: "These are incredibly exciting times for Nanologix. Seeing this study begin to crystallize has been invigorating, and it's wonderful to see other health care providers share an interest in our test, which is the leading diagnostic assay in bacterial identification and determination of antibiotic susceptibility. When speaking with nurses and other doctors, it's extraordinary to see their enthusiasm for the test --- we have found the right home for a study of this magnitude."
Jonathan Faro, MD Joins NanoLogix Board of Directors
Inbox
NanoLogix news@nanologix.com via icontactmail4.com
8:17 AM (12 hours ago)
NanoLogix Incorporated
NanoLogix Welcomes Dr. Jonathan Faro to Board of Directors
Jonathan Faro, PhD, MD, joins as Director of Medical Development
NanoLogix is pleased to announce the addition of Jonathan Faro, PhD, MD to the Company's Board of Directors. Dr. Faro is the co-inventor of the N-Assay modified ELISA bacteria-detection and identification technology and primary author of a number of published peer-reviewed research papers on the technology.
Dr. Faro's statement:
I am very excited to have joined the Board of Directors at NanoLogix, Inc. As the Director for Medical Development, I will serve a direct role in advocating for the goals of the company, and plan to work alongside the CEO and other board members to further development of the N-Assay. With their support, I have several goals that I aim to achieve. First and foremost, several studies need to be initiated. In addition to a large, multi-site study involving both private and academic centers, we will work on establishing multiple small-scale studies. Each of these will focus on the unique strengths of the N-Assay, so that clinicians will see that the assay is superior to anything currently on the market. We will focus on a four-pronged approach:
A) Speed of pathogen identification, providing clinicians with an accurate result far faster than that of culture,
Determination of antimicrobial resistance, so that clinicians may target their approach quickly, and begin seeing results faster than with any other technology on the market.
C) Offer clinicians novel approaches in treating infectious diseases, so that we stop the continued development of antimicrobial resistance.
D) Offer cheaper tests that do not increase the burden on national and international healthcare resources.
This final goal will have the benefit of taking NanoLogix not just through the US market, but will allow it to gain steady footing in the global market, which is necessary in order to truly help in limiting the spread of antimicrobial resistance, which currently claims approximately 700,000 lives per year. Although each of these goals will require considerable time, effort, and financial support, we have already begun the process of building in-roads with multiple well-respected clinical collaborators. These next several months certainly will be very exciting times for both myself and for NanoLogix!
NanoLogix Inc.
1- 330-534-0800
Email: info@nanologix.com // Website: http://www.nanologix.com
April 19,2018
Update On Petri FlatPack International Patent Status
Pursuant to NanoLogix' International Patent Offering
NanoLogix is pleased to announce payment yesterday (18 April 2018) of annuities for the FlatPack petri plate extended-life packaging patent in the EU and other granting countries. These annuity payments were made possible through a long time shareholder's efforts and the resulting receipt of funds by the Company from a new investor. The importance of the annuity payments cannot be overstated for the development of Nanologix --- sale and/or licensing of the FlatPack Patents internationally is projected to provide funding for the Company's expansion of agar-filled petri plate production in the USA and to complete development and pursue marketing of both the N-Assay modified ELISA rapid bacteria diagnostic test and its associated Pre-test.
Without the potential to monetize the international patent assets the Company's development would depend upon domestic organic growth only, a process that while steady, would not meet NanoLogix' needs for rapid expansion.
Posted On: 04/12/2018 12:44:04 PM
Posted By: Kachingpdx1
Further European Patent Office Information on FlatPack Patent for Sale and Licensing
International Patent Offering
NanoLogix is pleased to announce receipt today (dated 11 April 2018) of notice from the European Patent Office (EPO) of the expiration of the nine-month opposition filing period for the FlatPack petri plate extended-life packaging patent (European Patent No. 2699491). The reason for this update from Nanologix is to inform all interested parties that out of the fourteen signatory countries chosen and paid for the registration and validation of the Flatpack Patent in early September 2017, prior to the receipt of this notice from the EPO, of the signatory states for the EU Patent treaty only the three non-EU member states of Sweden, Croatia, and Turkey had published notice of validation of the Flatpack patent in their respective patent bulletins.
Notice from the EPO states: "The entry in the Register of European Patents will be automatically generated by the electronic data processing system".
Further information from this notice: "This European patent has become wholly equivalent to a bundle of national patents in the designated states in which the patent was validated".
The publication in the EU Patent Registry is the essential and final step to enable NanoLogix to offer a fully registered and validated patent in the EU for license and/or sale. This step is in accordance with the Company's stated goal of using receipts from those efforts to fund expansion of agar-filled petri plate production in the US and complete development and pursue marketing of both the N-Assay modified ELISA rapid bacteria diagnostic test and its associated Pre-test.
The Company is currently seeking to raise $30,000 for the April payment of the international annuities for the issued FlatPack patents and pending applications in the following countries:
Issued: China, New Zealand, Chile, Mexico, South Africa, UK, Germany, Sweden, France, Spain, Italy, Switzerland, Serbia, Croatia, Turkey, Denmark, Ireland, Poland, and the Netherlands.
Pending: Brazil, Canada
Posted On: 04/09/2018 11:28:36 AM
Posted By: Kachingpdx1
[4-9-18] Update on Patents Offered for Sale and Licensing, Grant Applications
International Patent Offering
NanoLogix is pleased to provide this update on the ongoing work on the sale and/or licensing of the international issued FlatPack patents, and filed and in-process applications to the National Institutes of Health, The National Science Foundation and BARDA
We have had interest in the technology from companies in France, Spain, Turkey, Serbia, South Africa, and China. The interest varies from licensing arrangements, purchase, and through direct representation of our products.
The Company is currently in the process of raising $30,000 for the April payment of the international annuities for the issued FlatPack patents and pending applications in the following countries:
Issued: China, New Zealand, Chile, Mexico, South Africa, UK, Germany, Sweden, France, Spain, Italy, Switzerland, Serbia, Croatia, Turkey, Denmark, Ireland, Poland, and the Netherlands.
Pending: Brazil, Canada
Grant Applications
One grant application has been filed with the National Institutes of Health (NIH) and two additional are planned with The National Science Foundation (NSF) and the Biomedical Advance Research and Development Authority (BARDA). Two of the applications are for funding for a pre-test for use with the N-Assay modified ELISA diagnostic and the BARDA application is for the use of the N-Assay for diagnostics of bio-threat agents.
As stated with the previous update from November, while there is strong competition for the grants, we believe the N-Assay and what it offers will be attractive to the grant evaluators.
i dont think they even read my posts or perhaps those of other longs
all my life i've seen ppl captured in prisons of their own making- thought patterns resulting from millions of decisions they have made that they cant even remember,let alone take responsibility for,but rather always look for a scapegoat-and in that tunnel which they cannot see outside of they are trapped-and cant find the answers which come from outside that tunnel
e.g why arent those familiar with dr faro buying nnlx stock by the millions?
well, to start with how many ppl even know of faros involvement in a no info company called nnlx????? very very few
they cant know unless
1) they read these stock boards-so how many do that -very very few -my best friend who dragged me into pennies didnt even know these stock boards existed
how many invest in a no info co-very very few- thats an important part of the answer but when i detailed that as an important part of the answer many years ago here i was heavily attacked by longs
bc its no info the only place to find info is the website or these boards
2) or unless they were involved in the private closed meetings-very very few were involved in those secret meetings bc as always big co's selfishly want their involvement hidden until they have successfully cornered the market and as usual has an nda
3- even if they know how many even know how to trade penny stocks -very very few
even if they know nanologix name how are non-traders even going to find the ticker and set up a brokerage acct and trade -very very few will -laziness- ppl dont like to go outside their comfort zones
4) buying stock- no matter how much- will not raise one cent to fund the study- funded from both Federal Grants and a raise of investment capital-8-20-18
and those who were involved in the secret meetings could not buy stock bc that would be insider trading-can they now? i dont know -a matter of interpretation-have all the material info from those secret meetings been distilled by nnlx in updates to stockholders who have signed up for updates? -for our part we've posted all those updates here and the board info
1of the disadvantages of a no info stock is the high likelihood of insider trading-which is why i have purposefully had no personal contact w the company while its otc no info
now naysayers should understand this/the mindset of breaking through stubborn resistance to break into the market
we know nnlx has a superior product in the n assay and petriplates
but outsiders want to see it proved- show me-they all live in the show me state- thats what studies are for -
nobody wants to buy the product until years of specialized studies -ISNT THAT HOW BIOTECH WORKS!!!!
THEY ARENT GOING TO MAKE AN EXCEPTION FOR LITTLE OLD NNLX-
nnlx did years of studies internally and years of studies outside before much traction w their superior petri plates
going thru the same process now w the n assay!!!!!
every company wants everything handed to them on a silver platter -all the work including modifications for their company already done -the way of the selfish world-and if the big co's dont get their way in everything they would rather pout and out than play
thats the very difficult game these small startups have to play-many such startups have had better products-but very few startups succeed-this is NOT unique to nnlx as some pretend in the blame game
many of the frustrations posted by posters re nnlx apply to almost all penny stocks-
but ppl forget why they got into penny stocks- blue chips have their frustrations also -chiefly is that retail traders cant compete w the saturated insider trading/supercomputers and fraud that is involved in blue chips
its frustrating to the nnlx officers etc also, as year after year goes by without being able to monetize their time and efforts-pure logic!
Posted On: 10/26/2018 9:16:31 AM
Posted By: Fibonacci233
Nanologix Incorporated
New write up that will be posted on our new website soon for our patented diagnostic. Comments and interest welcomed:
Nanologix' N-Assay offers an innovative solutions to a major problem that has plagued physicians over the years.
In medicine, nothing gets a clinician's attention like sepsis. When one has seen a patient who had previously been doing just fine suddenly take a turn for the worse, management decisions must be made without hesitation. In the case of a septic patient, seconds mean the difference between life and death, and minutes are a luxury that neither the clinician nor the patient may afford. The post-operative patient, the post-partum patient, the ICU patient... any patient is at risk of encountering a virulent pathogen in the hospital, and without an astute clinician ready to respond, serious consequences will occur. It's not surprising that the Infectious Disease Society of America estimates just this year that treating infections cost 21 to 34 billion dollars annually, in the US alone.
Clinicians currently have two techniques at their disposal when treating a presumed infection -culture, and PCR. The traditional technique of culture is labor intensive, requires laboratory-trained personnel, and correctly obtained, viable material. Although this method is relatively inexpensive, it is incredibly time-consuming. Patients often find it hard to believe that obtaining a culture result and antibiotic sensitivity profile may take 5 days! While the clinician is waiting for the results, they are throwing everything they've got at the possible infection. This is truly an empiric approach, and here it pays to have an experienced clinician by your side.
The alternative method, PCR, is much faster, much more sensitive, but also much more expensive. This newer technique also costs a great deal more, and requires highly trained personnel to operate the devices. These machines also incur a large capital investment by the hospital, as well as annual maintenance. In spite of the strengths of PCR, it also has weaknesses -it is unable to differentiate the difference between live/dead bacteria, and can not provide estimates relating to the degree of the inoculum. This information is essential for the clinician in directing targeted therapy, so again, they are ultimately forced to rely on their experience when treating the patient.
Regardless of one's opinion as to whether culture or PCR is the better option, the data over the last few decades shows the depressing truth -neither option is offering us any real advantage. This is made clear when one looks at the development of antibiotic resistance. These bugs have continued to grow and evolve, and a few years ago, a gonorrhea "super-bug" was isolated -showing resistance to every antibiotic available. We are clearly losing the war against these single-cell enemies!
In answer to this major problem, we have developed and patented an approach that takes all of the advantages of both culture and PCR (specificity, sensitivity, speed, and accuracy as well as ease of use), and none of the disadvantages. This technique, termed the N-Assay, is an antibody-based assay that targets potentially any bacterial pathogen (and has also been seen to detect yeast), in as little as 30 minutes. In addition, when incubated for 6 hours, this test not only provides a bacterial identification, but also allows the clinician to determine which antibiotic will work in treating the infection. This test will dramatically shorten the amount of time required for a clinician to wait when treating the ill patient, and should ultimately save billions in healthcare spending. Furthermore, by more accurately targeting the right bacterium with the correct antibiotic, we should drastically reduce the incidence in antimicrobial resistance.
We have already used a pilot version of this test in detecting group B streptococcus colonization in pregnant women, and have won an award at an OB GYN conference when presenting our data. The clinicians see that this test has tremendous potential, and are eager for it to be available, as they simply need better methods to more accurate diagnose infection. With the right resources, we will be able to expand this test to additional bacterial pathogens, such as E. coli, Enterococcus, MRSA, and any other clinically relevant pathogen.
Posted On: 09/07/2018 10:21:03 AM
Posted By: LuckyDog111
Notice of Upcoming NanoLogix Website Revision
Request For Confirmation of Continuing Interest From Newsletter Subscribers
NanoLogix is pleased to announce the Company website will be extensively revised and updated during September and October. The Company requests that those Newsletter Subscribers who are interested in continuing to receive updates of NanoLogix news through our iContact news service to send a confirmation email to: info@nanologix.com
This revision will enable the Company to significantly improve the website, providing the ability to respond rapidly to business events and to quickly furnishbusiness, technology, and hospital study updates.
8-20-18
NanoLogix Attends Series of Meetings In Houston
Preparation for Pre-test Development Study
NanoLogix is pleased to announce their attendance at a series of meetings in Houston with Drs. Sebastian and Jonathan Faro and the CEO of a California-based Biotechnology firm. The purpose of the meetings was for coordinating forces for a research study for development of a rapid pre-test for use with the patented Nanologix N-Assay bacteria diagnostic. The meetings dealt with organization and staffing of a research study at two major Houston hospitals, funded from both Federal Grants and a raise of investment capital , and the specific personnel required for the successful execution of the study. The personnel agreeing to participate in the study are seven MDs, two research nurses, two microbiologists, at least two laboratory technicians, and the CEO of the California Biotechnology company. NanoLogix personnel and the CEO of the Biotechnology company have signed a mutual non-disclosure agreement limiting what can presently be revealed but once funding has been obtained and the study registered with the FDA and initiated, the identity of the pre-test development company should be available as public knowledge.
The purpose of the pre-test use with the N-Assay is to have a pre-test that will indicate the presence of a specific bacteria with minutes, for which the N-Assay can then be used to rapidly determine both the concentration of the bacteria and its sensitivity to various antibiotics, furnishing Point of Care (POC) personnel the ability to effectively treat the patient with the specific antibiotic required. This development will significantly reduce reliance upon broad-spectrum antibiotics, which contribute to the major worldwide problem of the development of antibiotic-resistance for many bacteria.
NanoLogix has also agreed to fund an existing laboratory in Houston currently in use as a clinical laboratory for the medical group associated with Dr Jonathan Faro. This lab will be crucial to the testing of patient samples during the upcoming study.
Dr. Jonathan Faro, PhD, MD stated: "These are incredibly exciting times for Nanologix. Seeing this study begin to crystallize has been invigorating, and it's wonderful to see other health care providers share an interest in our test, which is the leading diagnostic assay in bacterial identification and determination of antibiotic susceptibility. When speaking with nurses and other doctors, it's extraordinary to see their enthusiasm for the test --- we have found the right home for a study of this magnitude."
Jonathan Faro, MD Joins NanoLogix Board of Directors
Inbox
NanoLogix news@nanologix.com via icontactmail4.com
8:17 AM (12 hours ago)
NanoLogix Incorporated
NanoLogix Welcomes Dr. Jonathan Faro to Board of Directors
Jonathan Faro, PhD, MD, joins as Director of Medical Development
NanoLogix is pleased to announce the addition of Jonathan Faro, PhD, MD to the Company's Board of Directors. Dr. Faro is the co-inventor of the N-Assay modified ELISA bacteria-detection and identification technology and primary author of a number of published peer-reviewed research papers on the technology.
Dr. Faro's statement:
I am very excited to have joined the Board of Directors at NanoLogix, Inc. As the Director for Medical Development, I will serve a direct role in advocating for the goals of the company, and plan to work alongside the CEO and other board members to further development of the N-Assay. With their support, I have several goals that I aim to achieve. First and foremost, several studies need to be initiated. In addition to a large, multi-site study involving both private and academic centers, we will work on establishing multiple small-scale studies. Each of these will focus on the unique strengths of the N-Assay, so that clinicians will see that the assay is superior to anything currently on the market. We will focus on a four-pronged approach:
A) Speed of pathogen identification, providing clinicians with an accurate result far faster than that of culture,
Determination of antimicrobial resistance, so that clinicians may target their approach quickly, and begin seeing results faster than with any other technology on the market. C) Offer clinicians novel approaches in treating infectious diseases, so that we stop the continued development of antimicrobial resistance.
D) Offer cheaper tests that do not increase the burden on national and international healthcare resources.
This final goal will have the benefit of taking NanoLogix not just through the US market, but will allow it to gain steady footing in the global market, which is necessary in order to truly help in limiting the spread of antimicrobial resistance, which currently claims approximately 700,000 lives per year. Although each of these goals will require considerable time, effort, and financial support, we have already begun the process of building in-roads with multiple well-respected clinical collaborators. These next several months certainly will be very exciting times for both myself and for NanoLogix!
NanoLogix Inc.
1- 330-534-0800
Email: info@nanologix.com // Website: http://www.nanologix.com
April 19,2018
Update On Petri FlatPack International Patent Status
Pursuant to NanoLogix' International Patent Offering
NanoLogix is pleased to announce payment yesterday (18 April 2018) of annuities for the FlatPack petri plate extended-life packaging patent in the EU and other granting countries. These annuity payments were made possible through a long time shareholder's efforts and the resulting receipt of funds by the Company from a new investor. The importance of the annuity payments cannot be overstated for the development of Nanologix --- sale and/or licensing of the FlatPack Patents internationally is projected to provide funding for the Company's expansion of agar-filled petri plate production in the USA and to complete development and pursue marketing of both the N-Assay modified ELISA rapid bacteria diagnostic test and its associated Pre-test.
Without the potential to monetize the international patent assets the Company's development would depend upon domestic organic growth only, a process that while steady, would not meet NanoLogix' needs for rapid expansion.
Posted On: 04/12/2018 12:44:04 PM
Posted By: Kachingpdx1
Further European Patent Office Information on FlatPack Patent for Sale and Licensing
International Patent Offering
NanoLogix is pleased to announce receipt today (dated 11 April 2018) of notice from the European Patent Office (EPO) of the expiration of the nine-month opposition filing period for the FlatPack petri plate extended-life packaging patent (European Patent No. 2699491). The reason for this update from Nanologix is to inform all interested parties that out of the fourteen signatory countries chosen and paid for the registration and validation of the Flatpack Patent in early September 2017, prior to the receipt of this notice from the EPO, of the signatory states for the EU Patent treaty only the three non-EU member states of Sweden, Croatia, and Turkey had published notice of validation of the Flatpack patent in their respective patent bulletins.
Notice from the EPO states: "The entry in the Register of European Patents will be automatically generated by the electronic data processing system".
Further information from this notice: "This European patent has become wholly equivalent to a bundle of national patents in the designated states in which the patent was validated".
The publication in the EU Patent Registry is the essential and final step to enable NanoLogix to offer a fully registered and validated patent in the EU for license and/or sale. This step is in accordance with the Company's stated goal of using receipts from those efforts to fund expansion of agar-filled petri plate production in the US and complete development and pursue marketing of both the N-Assay modified ELISA rapid bacteria diagnostic test and its associated Pre-test.
The Company is currently seeking to raise $30,000 for the April payment of the international annuities for the issued FlatPack patents and pending applications in the following countries:
Issued: China, New Zealand, Chile, Mexico, South Africa, UK, Germany, Sweden, France, Spain, Italy, Switzerland, Serbia, Croatia, Turkey, Denmark, Ireland, Poland, and the Netherlands.
Pending: Brazil, Canada
Posted On: 04/09/2018 11:28:36 AM
Posted By: Kachingpdx1
[4-9-18] Update on Patents Offered for Sale and Licensing, Grant Applications
International Patent Offering
NanoLogix is pleased to provide this update on the ongoing work on the sale and/or licensing of the international issued FlatPack patents, and filed and in-process applications to the National Institutes of Health, The National Science Foundation and BARDA
We have had interest in the technology from companies in France, Spain, Turkey, Serbia, South Africa, and China. The interest varies from licensing arrangements, purchase, and through direct representation of our products.
The Company is currently in the process of raising $30,000 for the April payment of the international annuities for the issued FlatPack patents and pending applications in the following countries:
Issued: China, New Zealand, Chile, Mexico, South Africa, UK, Germany, Sweden, France, Spain, Italy, Switzerland, Serbia, Croatia, Turkey, Denmark, Ireland, Poland, and the Netherlands.
Pending: Brazil, Canada
Grant Applications
One grant application has been filed with the National Institutes of Health (NIH) and two additional are planned with The National Science Foundation (NSF) and the Biomedical Advance Research and Development Authority (BARDA). Two of the applications are for funding for a pre-test for use with the N-Assay modified ELISA diagnostic and the BARDA application is for the use of the N-Assay for diagnostics of bio-threat agents.
As stated with the previous update from November, while there is strong competition for the grants, we believe the N-Assay and what it offers will be attractive to the grant evaluators.
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