Register for free to join our community of investors and share your ideas. You will also get access to streaming quotes, interactive charts, trades, portfolio, live options flow and more tools.
Register for free to join our community of investors and share your ideas. You will also get access to streaming quotes, interactive charts, trades, portfolio, live options flow and more tools.
An assay is a test. A blood card is not test, it's a blood collection device.
It's not an allergy/covid19 test. It's 2 separate tests.
The allergy test does not require FDA approval. The covid19 test does.
Coronavirus immunity tests are coming soon, Fauci says
4/10/20
I must have missed the PR that said
From all the articles I've read, the main difference between allergies and covid 19 is a FEVER.
Allergies never produce fever. Covid19 does.
So a thermometer may be a more cost effective solution than an allergy test that will result in allergy treatment.
G R E E D and the ARYC covid19 test
You say:
Or some people care more about the test, if it's as good as they say, reaching and helping millions of people by publicizing it, instead of Mark worrying about competition and keeping it quiet to make more money for himself.
Give me a break. You mean to tell me that in the current pandemic with so many people dying and the shortage of tests being a critical issue that Mark is worried about
Where is Arrayit's PR and scientific papers about it, and coverage in the main media.
Can't just take Marc Jablonski's and his website word for it
I'd like to believe
'extreme sensitivity of the test can detect virus in most cases earlier that the nasopharyngeal swab test'
But if that was the case why isn't ARYC shouting that from the rooftop but instead depends on Jablonki and the like to quietly spread the word on their websites.
Oh!! It's crystal clear now! The video says select the box for the covid test! I can see the stampede of doctors rushing to check that box for an unknown test. LOL
It just shows a box to order the covid test.
How is that "fully explained".
The test is pretty much a "black box". Doubt that a significant number of doctors will order the test until scientific details are provided by Arrayit about the test.
Most doctors are science based, and don't take the word of salespeople without proof.
Serological Rapid Test Is Not A Replacement For RT-PCR Tests
Novel coronavirus SARS-CoV-2/COVID-19 serological tests based on detecting antibodies in the blood and nucleic acid tests based on detecting the virus using reverse transcription and the polymerase chain reaction (RT-PCR) are complementary rather than competing approaches. Because of the relatively short time since the outbreak and the rather limited testing and demographic data available, we are currently assembling detailed clinical performance benchmarks, including analytical specificity, analytical sensitivity, and other parameters. By extrapolation to testing on other viruses, including the causative agents of Severe Acute Respiratory Syndrome (SARS) and Middle East Respiratory Syndrome (MERS), PCR tests and serological tests have been used for a long time by health professionals to identify various infections with considerable reliability (see references).
For patients who are asymptomatic and want to be tested to obtain greater information about possible exposure, PCR and serological testing may both produce satisfactory results depending on the time and extent of exposure, individual immune response and other factors.
The time between exposure and antibody production (seroconversion time) is probably 3-15 days for SARS-CoV-2/COVID-19. During this period, even if the person is exposed to the virus or has been identified as positive by RT- PCR, a serological test may score negative if the antibody level in the blood specimen is below the analytical sensitivity of the blood test. So the recommendation for symptomatic patients is that their first testing should be absolutely a PCR test, NOT A SEROLOGICAL TEST. Below are some recommendations with respect to patient symptoms and test results to guide the use of the serological Rapid Test:
1. Patients with COVID-19 symptoms
These patients can be tested using a COVID-19 Rapid Test; however, we strongly recommend a follow-up RT-PCR test if the serological test results are negative. This recommendation is based on the 3-15 day seroconversion time.
2. Patients that score negative by RT-PCR
The COVID-19 Rapid Test is fast, affordable, and can be deployed multiple times per patient. We recommend the Rapid Test for patients with negative RT-PCR test results because nucleic acid testing requires the presence of viral particles and, therefore, may not provide a good measure of exposure.
3. Patients who have been diagnosed with COVID-19 and have recovered from the illness
RT-PCR testing requires the presence of viral particles and may produce a negative test result on patients who have recovered from COVID-19.
Because COVID-19 IgG antibodies are highly stable and remain in the bloodstream for a long period following COVID-19 infection, the Rapid Test is highly recommended for these patients as an indication of past infection and immunity.
4. Patients seeking to verify a positive RT-PCR test result
RT-PCR tests generally have very high analytical sensitivity (i.e. can identify a relatively low titer of virus in a nasal swab) but depending on the testing platform may produce a relatively high rate of false positives (i.e. a positive test result on a patient who is negative for the COVID-19 virus). Under these circumstances, confirmatory testing using a serological Rapid Test is highly recommended as a means of either confirming a positive test result or identifying a potential false positive.
5. Patients with seasonal allergies
Because we are entering peak allergy season, patients with mild or acute rhinitis and other allergy symptoms are excellent candidates for both serological allergy testing and the COVID-19 Rapid Test as an important means of distinguishing between seasonal allergies and coronavirus
https://www.rapidc19.com/infection.
Yes we need detailed info about the Arrayit test, not just bits and pieces from vendors website/videos.
We need to what exactly are the measuring, and what it means to the patient.
Pinner USA's is a blood test, requires one drop, it's done at the point of care and takes minutes to get results. Pinner put out a ton of details about the rapid test that they the licensed from China. In addition to IgG they also measure IgM which is present 3-5 days after infection.
Rapid tests are less accurate. According to the website, IgG has an accuracy of 100% and, IgM has an accuracy of 90.0%.
What exactly is Arrayi's accuracy and at what point of the infection,
https://www.rapidc19.com/
https://www.wfmj.com/story/41954664/pinner-c9-covid19-finger-prick-blood-test-results-in-minutes
Yes it is. One thing I'd like to know, about the ARCY antibody test is if it detects current infection before the 8th day after infection.
Per allergydx video: "IgG covid microarray test checks for reactivity to 12 proteins specific to the covid virus" .... antibodies=proteins
AlliQ website says
You can't order the test directly @ covid-19@arrayit.com it has to be ordered by a doctor.
But according to the alliq website on their page, you can submit a form to be connected to a tele-doctor.
https://www.alliq.bio/get-started
My google search showed this:
WELLMED :: OpenCorporatesopencorporates.com › companies › us_ca
30 LIBERTY SHIP WAY, STE. 3010. SAUSALITO CA 94965; United States. Agent Name: TRAVIS CECIL WHITAKER; Agent Address: 30 LIBERTY SHIP WAY, ...
TATE LABS, INC. :: OpenCorporatesopencorporates.com › companies › us_ca
Free and open company data on California (US) company TATE LABS, INC. (company number ... 30 LIBERTYSHIP WAY SUITE 3010 SAUSALITO CA 94965 ...
In Italy, Going Back to Work May Depend on Having the Right Antibodies
Weighing an idea that might once have been relegated to science fiction, Italy once again finds itself in the unfortunate vanguard of Western democracies grappling with the coronavirus.
Having the right antibodies to the virus in one’s blood — a potential marker of immunity — may soon determine who gets to work and who does not, who is locked down and who is free.
https://www.nytimes.com/2020/04/04/world/europe/italy-coronavirus-antibodies.html
Telemedicine: ‘10 Years of Change in One Week’
With the coronavirus pandemic turning doctors’ offices into no-go zones, family physicians are now doing many of their consultations online or by telephone.
https://www.nytimes.com/2020/04/04/world/europe/telemedicine-uk-coronavirus.html
The telemedicine/allergy/covid tests solution is good news, and the video explains that the microarray covid test is IgG testing reactivity to 12 proteins specific to covid. That's a lot of details we did not know before.
And the vendor network should be able to sell the concept very easily to clinics and doctors offices. Already about 1,000 doctors and clinics are on the ARYC patient data solutions portal, so they could add covid testing and telemedicine pretty easily.
Insurance covers the testing and telemedicine visits
The video said FDA approved blood card. Arrayit has never received an FDA approval for any of its products. They are using a card manufactured by someone else.
https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm
It's not clear to everyone. I've seen a lot of posts today just talking about FDA approval without any qualifications
Blood collection device is a blood card. Not the covid test.
Show me exact point in the video "she" said that the Arrayit covid test is FDA approved
GP said the covid test was approved, And pointed at a different video. You're talking about a different video/product
Arrayit covid test is not FDA approved yet. But under the guidelines they can sell it if they submitted an EAU application
Please point to where in the video it says it's FDA approved. The only mention about covid is at around the 1:20 minute mark to check the box if you want to order it.
https://vimeo.com/400954846
As of noe, the dissemination is vendors like Jablonski selling the telemedicine/covid concept to doctors offices/clinics.
The patient portal probably has over 1,000 doctors/clinics signed on to it.
The PR they put out on April of last year said that the count was over 700. And new ones were announced on twitter every day until they stopped tweeting all together in Aug 2019.
If they have millions of kits in inventory, that should put their assets over $10M = they need to file fins by end of April. IMO
No. What they are doing is using the blood on the blood card to run two different tests. One for allergies and one for covid.
I like the video and the telemedicine solution for covid/allergies tests.
But just because Jablonski said that the blood cards are FDA approved doesn't make it so. What he probably meant is the the FDA is OK with the use of whole blood cards, and they don't need FDA approval.
The other Arrayit blood card that separates the blood into its components is the one that needs FDA approval.
On the video Jablonski said the the IgG covid microarray test checks for reactivity to 12 proteins specific to the covid virus,
Pinner USA, which markets pinnertest processed in Arrayit's lab.
announced Pinner C19 rapid test using Hangzhou Biotest Biotech’s COVID-19 IgG/IgM Rapid Test Cassette. It's processed in clinics and doctors offices
https://www.rapidc19.com/
https://www.wfmj.com/story/41954664/pinner-c9-covid19-finger-prick-blood-test-results-in-minutes
Pinner C9, Covid-19 Finger Prick Blood Test: Results in Minutes
Pinner USA presents Pinner C19, a rapid Covid-19 test performed via chromatographic immunoassay for the qualitative detection of IgG and IgM antibodies to SARS-CoV-2 in whole human blood, serum or plasma.
Pinner C19 Rapid Covid-19 test was developed and produced in China by our production partner in which has met the stringent quality management system audits of CFDA (Chinese Food and Drug Administration) and ISO 13485 and has recently received World Health Organization (WHO) certification. The CDC of China has evaluated this test. According to their conclusion, IgG has an accuracy of 100% and, IgM has an accuracy of 90.0%.
Thanks. Things are moving fast for companies to catch up.
Sloan, I could not find covid19 test on dXAllergy Solutions at https://dxallergy.com/
Thanks for sharing the other video too.
https://www.usatoday.com/story/news/world/2020/03/18/coronavirus-did-president-trumps-decision-disband-global-pandemic-office-hinder-response/5064881002/
WASHINGTON—In May 2018, President Donald Trump’s biodefense preparedness adviser warned that a flu pandemic was the country’s No. 1 health security threat, and the U.S. was not prepared.
“We know that it cannot be stopped at the border,” Luciana Borio, director of medical and biodefense preparedness at the National Security Council, said at a symposium that day.
Borio left the Trump administration in 2019. Other high-level global health experts headed for the exits even earlier, after the White House dismantled the National Security Council’s global health security office.
The demise of that elite team is now under scrutiny as the Trump administration struggles to respond to the coronavirus pandemic.
Trump bristled when asked about his decision to disband the office at a news conference in the Rose Garden on Friday.
“I just think it's a nasty question,” the president responded. “And when you say ‘me,' I didn't do it. ... I don't know anything about it.”
Thanks!
Is Iconic court date conference still on for tomorrow?
I know that Iconic filed on 3/16 for a 2 month postponement of the trial to work out a settlement, but the San Diego court has not responded as far as the website says.
Future events:
04/03/2020 10:15 AM C-67 Trial Readiness Conference (Civil)
04/17/2020 08:30 AM C-67 Civil Jury Trial