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3 cents is soaring?
So youre saying that is just a bedside routine? Will they have interns doing that? No training needed?
Yeah just go to the gas station and get your led so you can inhale a light into your lungs to treat any lung issues! Sounds legit to me...
I doubt this will make AYTU any money. This is an evasive surgery that would require a surgeon and the patient being under anesthesia. This would be a last resort and wouldn't be used without training. Who is doing the training and who has time to bring very one to surgery?
How is that when the total volume of the day is 10-20 million shares if we're lucky?
Sounds like they don't believe the light can help most patients. That there is something else going on and offloaded the light to anyone that wanted it.
https://www.yahoo.com/news/alarmed-covid-patients-blood-thickened-133547956.html
Why are posters still trying to use the NBC New article?
China says no plans to limit export of anti-virus supplies - ABC News https://t.co/fa8Ja1USQV
— Josh Disbrow (@josh_disbrow) April 17, 2020
4 million is not small. A drop to $1.10
Does this sound legit? Isn't this working around the agreement with AYTU?
https://tucson.com/business/tucson-labs-develop-tests-to-help-fight-coronavirus-outbreak/article_61a60ccc-c7e0-55ca-bf99-682df3635d6f.html
AYTU does not have an EUA. AYTU falls here. This is what is going to be modified. This most likely won't affect AYTU's right to distribute because other countries have already performed the tests to ensure accuracy so they have a lot to back up their tests.
Per FDA web page
https://www.fda.gov/medical-devices/emergency-situations-medical-devices/faqs-diagnostic-testing-sars-cov-2
Q: Can I offer my SARS-CoV-2 antibody test kit in the US without an EUA?
A: As stated in Section IV.D of the FDA's Policy for Diagnostic Tests for Coronavirus Disease-2019, during the COVID-19 public health emergency, the FDA does not intend to object to the development and distribution by commercial manufacturers, or development and use by laboratories, of serology tests to identify antibodies to SARS-CoV-2, where the test has been validated, notification is provided to FDA, and information along the lines of the following is included in the test reports:
This test has not been reviewed by the FDA.
Negative results do not rule out SARS-CoV-2 infection, particularly in those who have been in contact with the virus. Follow-up testing with a molecular diagnostic should be considered to rule out infection in these individuals.
Results from antibody testing should not be used as the sole basis to diagnose or exclude SARS-CoV-2 infection or to inform infection status.
Positive results may be due to past or present infection with non-SARS-CoV-2 coronavirus strains, such as coronavirus HKU1, NL63, OC43, or 229E.
To help to ensure the above information is provided in the test report, as described in the guidance, commercial manufacturers could include this information in their Instructions for Use (IFU) or other labeling provided to laboratories.
As noted in the guidance, this policy does not apply to at home testing.
The commercial manufacturers and laboratories that have notified FDA that they have validated and are offering serology tests as set forth in Section IV.D of the FDA's Policy for Diagnostic Tests for Coronavirus Disease-2019 are listed on this FAQ page under What serology tests are being offered under the policy outlined in Section IV.D of the Policy for Diagnostic Tests for Coronavirus Disease-2019?.
More selling than buying going on
Q: What serology tests are being offered under the policy outlined in Section IV.D of the Policy for Diagnostic Tests for Coronavirus Disease-2019?
A: As stated in Section IV.D of the FDA's Policy for Diagnostic Tests for Coronavirus Disease-2019, the FDA does not intend to object to the development and distribution by commercial manufacturers, or development and use by laboratories, of serology tests to identify antibodies to SARS-CoV-2, where the test has been validated, notification is provided to FDA, and information along the lines of the following is included in the test reports:
This test has not been reviewed by the FDA.
Negative results do not rule out SARS-CoV-2 infection, particularly in those who have been in contact with the virus. Follow-up testing with a molecular diagnostic should be considered to rule out infection in these individuals.
Results from antibody testing should not be used as the sole basis to diagnose or exclude SARS-CoV-2 infection or to inform infection status.
Positive results may be due to past or present infection with non-SARS-CoV-2 coronavirus strains, such as coronavirus HKU1, NL63, OC43, or 229E.
This policy does not apply to at home testing.
The commercial manufacturers and laboratories listed below have notified FDA that they have validated and are offering serology tests as set forth in Section IV.D of the FDA's Policy for Diagnostic Tests for Coronavirus Disease-2019. The FDA has not reviewed the validation of tests offered by these developers, who may not be pursuing EUAs, and is including this list here to provide transparency regarding the notifications submitted to FDA.
Laboratory Notifications:
Arrayit Corporation
Beaumont Health
Boston Heart Diagnostics
DLS Research & Ventures
EDP Biotech Corporation
Emory Medical Laboratories
IMMYLabs
Mayo Clinic
Michigan Health Clinics
Otogenetics
Roseland Community Hospital/American Medical Lab
University of Minnesota Advanced Research and Diagnostic Laboratory
Vibrant America Clinical Labs
Manufacturer Notifications:
Abbott Laboratories SARS-CoV-2 IgG (for use on ARCHITECT)
Alfa Scientific Designs, Inc. Instant-view plus COVID-19 IgG/IgM Antibody Test
Alfa Scientific Designs, Inc. Clarity COVID-19 IgG/IgM Antibody Test
Assure Tech (Hangzhou) Co., Ltd.'s COVID-19 IgG/IgM Rapid Test Device
Atlas Link (Beijing)Technology Co., Ltd NovaTest: One Step COVID-19 IgG/IgM rapid test
Autobio Diagnostics' Anti-SARS-CoV-2 Rapid Test
Beijing Beier Bioengineering Co., Ltd 2019-New Coronavirus IgG/IgM Rapid Test Cassette (WB/S/P)
Beijing Decombio Biotechnology Co., Ltd. Novel Coronavirus IgM/IgG Combo Rapid Test-Cassette (Serum/Plasma/Whole blood)
Beijing Diagreat Biotechnologies Co., Ltd. 2019-nCoV IgG Antibody Determination Kit
Beijing Diagreat Biotechnologies Co., Ltd. 2019-nCoV IgM Antibody Determination Kit
Beijing Diagreat Biotechnologies Co., Ltd. 2019-nCoV IgG/IgM Antibody Rapid Test Kit
Beijing Kewei Clinical Diagnostic Reagent Inc. Genonto RapidTest10 COVID-19 IgG/IgM Antibody Rapid Test Kit
Beijing O&D BIOTECH Co., LTD. Coronavirus disease(COVID-19) Total Antibody Rapid Test (Colloidal Gold)
Beijing Wantai Biological Pharmaceutical Co., Ltd. TOTAL ANTIBODY WANTAI SARS- COV-2 Ab Rapid Test Kit
Beroni Group SARS-CoV-2 IgG/IgM Antibody Detection Kit
Biobase Biodustry (Shandong) Co., Ltd SARS-CoV-2 IgM/IgG Antibody Test Kit (Colloidal Gold)
Biohit Healthcare (Hefei) Co., Ltd. SARS-CoV-2 IgM/IgG antibody test kit (Colloidal Gold Method)
Biolidics Limited 2019-nCoV IgG/IgM Detection Kit (Colloidal Gold)
BioMedomics, Inc. COVID-19 IgM-IgG Rapid Test
BioSys Laboratories, Inc. BioSys Plus COVID-19 IgM/IgG Rapid Test
BTNX, Inc. Rapid Response™ COVID-19 IgG/IgM Test Cassette
Chembio Diagnostic Systems, Inc. DPP COVID-19 IgM/IgG System
Core Technology Co., Ltd. CoreTest COVID-19 IgM/IgG Ab Test
Core Technology Co., Ltd. RapidTest COVID-19 IgM/IgG Ab Test
Coronacide™ COVID-19 IgM/IgG Rapid Test
CTK Biotech, Inc. OnSite® COVID-19 IgG/IgM Rapid Test
DIALAB(ZJG) Biotech Co., Ltd. Device Name: SARS-CoV-2 IgG/IgM Antibody Test (Fluorescence Immunoassay)
Diazyme Laboratories, Inc. Diazyme DZ-LITE SARS-CoV-2 IgG CLIA Kit
Diazyme Laboratories, Inc. Diazyme DZ-Lite SARS-Cov-2 IgM CLIA Kit
Diazyme Laboratories, Inc. Diazyme SARS-CoV-2 Antibody Rapid Test
Eachy Biopharmaceuticals Co., Ltd. AccuRapid™ SARS-CoV-2 IgM/IgG Test Kit (Lateral Flow Immunoassay)
Eachy Biopharmaceuticals Co., Ltd. SmartScreen COVID-19 IgM/IgG Test Kit
EpiGentek SeroFlash SARS-CoV-2 IgM/IgG Antibody Detection Kit
Epitope Diagnostics, Inc. KT-1032 EDI™ Novel Coronavirus COVID-19 IgG ELISA Kit
Epitope Diagnostics, Inc. KT-1033 EDI™ Novel Coronavirus COVID-19 IgM ELISA Kit
ET Healthcare Inc. Pylon COVID-19 IgM/IgG Assay
EUROIMMUN AG Anti-SARS-CoV-2 ELISA (IgA)
EUROIMMUN AG Anti-SARS-CoV-2 ELISA (IgG)
GenBody Inc. GenBody COVID-19 IgM/IgG
Genrui Biotech Inc. Novel Coronavirus (2019-nCoV) IgG/IgM Test Kit (Colloidal Gold)
Getein Biotech Inc. One Step Test for Novel Coronavirus (2019-nCoV) IgM/IgG antibody (Colloidal Gold)
Goldsite Diagnostics Inc SARS-CoV-2 IgG/IgM ki
Guangzhou Fenghua Bioengineering Co., Ltd. SARS-CoV-2 IgG/IgM Rapid Testt
Guangzhou Wondfo Biotech Co., Ltd. SARS-CoV-2 Antibody Test
Hangzhou AllTest Biotech Co., Ltd. AllTest 2019-nCoV IgG/IgM Rapid Test Cassette
Hangzhou AllTest Biotech Co., Ltd. AllTest COVID IgG/IgM Rapid Test Dipstick
Hangzhou Clongene Biotech Co., Ltd. Clungene COVID-19 IgM/IgG Rapid Test Cassette
Hangzhou Clongene Biotech Co., Ltd. COMBRA COVID-19 IgM/IgG Rapid Test Cassette
Hangzhou Biotest Biotech's COVID-19 IgG/IgM Rapid Test Cassette
Hangzhou Realy Tech Co Ltd. 2019-nCOV IgG/IgM Rapid Test
Hangzhou Testsealabs Biotecnology Co., Ltd One Step SARS-CoV2 (COVID-19) IgG/IgM Test
Healgen Scientific, LLC. COVID-19 IgG/IgM Rapid Test Cassette(Whole Blood/Serum/Plasma)
Hunan RunKun Pharmaceutical Co., Ltd SARS-CoV-2 IgM/IgG Test Kit (Colloidal Gold)
INNOVITA (Tangshan) Biological Technology Co., Ltd. 2019-nCoV Ab Test (Colloidal Gold)
Jiangsu Dablood Pharmaceutical Co, Ltd. AssuranceAB™ COVID-19 IgM/IgG Rapid Antibody Test
Jiangsu Dablood Pharmaceutical Co. Ltd. COVID-19 IgM/IgG Rapid Test
Jiangsu Macro & Micro-Test Med-Tech Co., Ltd. SARS-CoV-2 IgM/IgG Rapid Assay Kit (Colloidal Gold)
Lepu Medical Technology (Beijing) Co., Ltd. Lepu SARS-CoV-2 Antibody Test (colloidal gold immunochromatography)
Lifeassay Diagnostics (Pty) Ltd Test-it COVID-19 IgM/IgG Lateral Flow Assay
Liming BioProducts Co. Ltd. SARS-CoV-2 lgM/lgG Antibody Rapid Test
Maccura Biotechnology Co., Ltd. Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) IgM/IgG Antibody Assay Kit by Colloidal Gold Method
Medical Systems Biotechnology Co., Ltd. Coronavirus Disease 2019 Antibody (IgM/IgG) Combined Test Kit
Mokobio Biotechnology R&D Center SARS-CoV-2 IgM & IgG Quantum Dot Immunoassay
Nanjing Liming Bio-products Co.,Ltd SARS-CoV-2 IgM/IgG Antibody Rapid Test Kit
NanoResearch, Inc. NanoMedicina™ SARS-COV-2 IgM/IgG Antibody Rapid Test
Nantong Diagnos Biotechnology Co., Ltd. (2019-nCoV) New coronavirus Antibody Test (Colloidal Gold)
Nirmidas Biotech, Inc. COVID-19 (SARS-CoV-2) IgM/IgG Antibody Detection Kit
PCL Inc. COVID19 IgG/IgM Rapid Gold
Phamatech Inc. COVID19 IgG/IgM Rapid Test
RayBiotech, Inc. Novel Coronavirus (SARS-CoV-2) IgG Antibody Detection Kit (Colloidal Gold Method)
RayBiotech, Inc. Novel Coronavirus (SARS-CoV-2) IgM Antibody Detection Kit (Colloidal Gold Method)
Safecare Biotech (Hangzhou) Co., Ltd SAFECARE COVID-19 IgG/IgM Rapid Test Device
SD Biosensor STANDARD Q COVID-19 IgM/IgG Duo
Shanghai Eugene Biotech Co., Ltd. SARS-CoV2 (COVID-19) IgG/IgM Rapid Test
Shanghai Liangrun Biomedicine Technology Co., Ltd. Liangrun COVID-19 IgM/IgG Antibody Test
Shenzhen Landwind Medical Co., Ltd COVID-19 IgG/IgM Rapid Test Device
Shenzhen Watmind Medical Co. SARS-CoV-2 IgG/IgM Ab Diagnostic Test Kit
Sugentech, Inc. SGTi-flex COVID-19 IgM/IgG
Sure Bio-tech API Covid-Rapid IgM/IgG Antibody Test Kit
Suzhou Kangheshun Medical Technology Co., Ltd SARS-CoV-2 IgG/IgM Rapid Test Cassette
Telepoint Medical Services SARS-CoV-2 IgG/IgM Rapid Qualitative Test
Tianjin Beroni Biotechnology Co. Ltd SARS-CoV-2 IgG/IgM Antibody Detection Kit
United Biomedical, Inc. UBI® SARS-CoV-2 ELISA
VivaChek Biotech (Hangzhou) Co., Ltd. VivaDiag COVID-19 IgM/IgG Rapid Test
W.H.P.M. Inc., COVID-19 IgM/IgG Rapid Test
W.H.P.M. Inc., COVISURE™ COVID-19 IgM/IgG Rapid Test
Wuhu 3H Biotechnology Co. Ltd. COVID-19 IgG/IgM Test Kit (Colloidal Gold Method)
Xiamen AmonMed Biotechnology Co. Ltd Helix-19 COVID-19 IgM/IgG Test Kit (Colloidal Gold)
Zhejiang GENE SCIENCE Co., Ltd Novel Coronavirus (2019-nCoV) IgM/IgG Antibodies Detection Kit (Latex Chromatography)
Zhejiang Orient Gene Biotech, Co., Ltd. COVID-19 IgG/IgM Rapid Test Cassette
Zhengzhou Fortune Bioscience Co., Ltd. COVID-19 IgG Antibody Rapid Test Kit (Colloidal Gold Immunochromatography method)
Zhengzhou Fortune Bioscience Co., Ltd. COVID-19 IgM Antibody Rapid Test Kit (Colloidal Gold Immunochromatography method)
Zhengzhou Fortune Bioscience Co., Ltd. COVID-19 Antibody Rapid Test Kit (Colloidal Gold Immunochromatography method)
Zhongshan Bio-Tech Co. Ltd SARS-CoV-2 IgM/IgG (GICA)
Zhuhai Encode Medical Engineering Co., Ltd Novel Coronavirus (COVID-19) IgG/IgM Rapid Test Device
Zhuhai Livzon Diagnostics, Inc. Diagnostic Kit for IgM/IgG Antibody to Coronavirus (SARS-CoV-2) (Colloidal Gold)
Test Kit Manufacturers and Commercial Laboratories Table:
Search:
Show 102550100All entries
Date EUA IssuedManufacturer4/14/2020Chembio Diagnostic System, Inc4/14/2020Ortho Clinical Diagnostics, Inc.04/10/2020Atila BioSystems, Inc.04/08/2020DiaCarta, Inc04/08/2020Becton, Dickinson & Company04/07/2020InBios International, Inc04/06/2020Gnomegen LLC04/03/2020Co-Diagnostics, Inc.04/03/2020ScienCell Research Laboratories04/03/2020Luminex Corporation04/02/2020Becton, Dickinson & Company (BD)04/01/2020Ipsum Diagnostics, LLC04/01/2020Cellex Inc.03/30/2020QIAGEN GmbH03/30/2020NeuMoDx Molecular, Inc.03/27/2020Luminex Molecular Diagnostics, Inc.03/27/2020Abbott Diagnostics Scarborough, Inc.03/26/2020BGI Genomics Co. Ltd03/25/2020Avellino Lab USA, Inc.03/24/2020PerkinElmer, Inc.03/23/2020Mesa Biotech Inc.03/23/2020BioFire Defense, LLC03/20/2020Cepheid03/20/2020Primerdesign Ltd.03/19/2020GenMark Diagnostics, Inc.03/19/2020DiaSorin Molecular LLC03/18/2020Abbott Molecular03/17/2020Quest Diagnostics Infectious Disease, Inc.03/17/2020Quidel Corporation03/16/2020Laboratory Corporation of America (LabCorp)03/16/2020Hologic, Inc.03/13/2020Thermo Fisher Scientific, Inc.03/12/2020Roche Molecular Systems, Inc. (RMS)02/29/2020Wadsworth Center, New York State Department of Public Health's (CDC)02/04/2020Centers for Disease Control and Prevention's (CDC)
And if you read and open the link it says only one company, Cellex in north Carolina. Was granted an actual EUA as of April 7th
More than 70 companies have notified the FDA that they have serological tests
https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-serological-tests
Coronavirus (COVID-19) Update: Serological Tests
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For Immediate Release:April 07, 2020Statement From:
Commissioner of Food and Drugs - Food and Drug Administration
Stephen M. Hahn M.D.
Serological tests measure the amount of antibodies or proteins present in the blood when the body is responding to a specific infection, like COVID-19. In other words, the test detects the body’s immune response to the infection caused by the virus rather than detecting the virus itself. In the early days of an infection when the body’s immune response is still building, antibodies may not be detected. This limits the test’s effectiveness for diagnosing COVID-19 and why it should not be used as the sole basis to diagnose COVID-19.
Serological tests can play a critical role in the fight against COVID-19 by helping healthcare professionals to identify individuals who have overcome an infection in the past and have developed an immune response. In the future, this may potentially be used to help determine, together with other clinical data, that such individuals are no longer susceptible to infection and can return to work. In addition, these test results can aid in determining who may donate a part of their blood called convalescent plasma, which may serve as a possible treatment for those who are seriously ill from COVID-19. This is why Vice President Mike Pence called on the laboratory community to develop serological tests for COVID-19.
In March, the FDA issued a policy to allow developers of certain serological tests to begin to market or use their tests once they have performed the appropriate evaluation to determine that their tests are accurate and reliable. This includes allowing developers to market their tests without prior FDA review if certain conditions outlined in the guidance document are met. The FDA issued this policy to allow early patient access to certain serological tests with the understanding that the FDA has not reviewed and authorized them.
The FDA can also authorize tests for COVID-19 under an Emergency Use Authorization (EUA). To date, FDA has authorized one EUA for a serological test that is intended for use by clinical laboratories.
Since the FDA issued the policy, over 70 test developers have notified the agency that they have serological tests available for use. However, some firms are falsely claiming that their serological tests are FDA approved or authorized, or falsely claiming that they can diagnose COVID-19. The FDA will take appropriate action against firms making false claims or marketing tests that are not accurate and reliable.
The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation’s food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.
How did I do that?
Ummm that is true. That is the definition of an Emergency Use. That was straight from the FDA website. Copy and pasted. It doesn't matter how well it does. I distributor cannot get final approval to sell a medication through the FDA.
A reseller cannot get approval. The Chinese company needs to file for approval. Then distributors can sell it after. Show one place where the manufacturer of these tests is filing for FDA APPROVAL. its not needed. This is all a temporary thing for AYTU to sell these.
Read the definition of an EUA on the FDA website.
• If authorized, the EUA means that this COVID-19 IVD is temporarily authorized for use until the public health emergency is terminated or the EUA is revoked by the FDA.
I'm not your teacher. I have referred to the articles you posted. I took snippets from those articles to give the information. If you haven't read them I don't need to repost them. That's silly for me to repost what you posted
I agree
I am not posting anything false.
An EUA is only good during an emergency. This is for a limited time by definition. Once US companies can keep up with demand it is no longer an emergency.
It was in the article you posted. I just copied it so you could read it.
AYTU is going to make money. These tests will help them be net positive for the quarter. But Abbott is going to blow them away. Once Abbott and other US companies meet the demands AYTU will not be able to sell under an emergency declaration.
Abbott Laboratories announced the launch of its third test for the coronavirus and said it could be screening 20 million people for antibodies for Covid-19 by June.
Abbott said it plans to distribute 4 million of the new tests by the end of this month, after an initial shipment of 1 million tests this week to U.S. customers.
“Antibody testing is an important next step to tell if someone has been previously infected,” Abbott said.
Do the math as well AYTU CANT deliver 10 million tests by the end of June. They need to sell all of them to order more and its taking 2 weeks from order to delivery. They just ordered another 1 million. So they will be lucky to sell and deliver 5 million by the end of June.
Abbott Laboratories Inc on Wednesday launched a coronavirus blood test that could show whether a person has been infected and plans to ramp up manufacturing to produce 20 million tests in June.
So they have already launched and expect an antibody test , to show the same thing as AYTU tests, and expect to have 20 million tests by the end of June.
Did you read the title of the article you posted?
Abbott launches antibody test for coronavirus, plans to deliver 20 million tests by June
My point exactly! So why are so many saying they have $60 million in the bank?
Show proof of that too! No matter what all this money is in China's hands so they can get product as fast as possible. ATU is not sitting on $60 million. If they are show proof
Yes with profit! But if they make a purchase they no longer have they money. So they don't have $60 million cash, do they? They keep investing this money in product so they don't have this money do they?
Will someone please post proof of the alleged $60 million? I doubt they have this on hand. It is probably being used to buy the Chinese test kits. They probably need to pay for these when they order them. They are requesting more than they originally planned because they have raised more money to purchase them. So I highly doubt they are sitting on this money like it is being led to believe
Abbott has two other testes on the market and say they can produce 20 million rapid tests a month. They are a US company so they will be mentioned by Trump before ATU
This is completely untrue. There are a dozen rapid tests that were cleared by the fda
These risks and uncertainties include, among others: market and other conditions, the regulatory and commercial risks associated with introducing the COVID-19 IgG/IgM Rapid Test, shipping delays and their impact on our ability to introduce the COVID-19 IgG/IgM Rapid Test, our ability to enforce our exclusive rights to distribute the COVID-19 IgG/IgM Rapid Test in the jurisdictions set forth in the distribution agreement, the ability of the COVID-19 IgG/IgM Rapid Test to accurately and reliably test for COVID-19, the manufacture of the COVID-19 IgG/IgM Rapid Test’s ability to manufacture such testing kits on a high volume scale, manufacturing problems or delays related to the COVID-19 IgG/IgM Rapid Test, our ability to satisfy any labelling conditions or other FDA or other regulatory conditions to sell the COVID-19 IgG/IgM Rapid Test Kit, the ability to obtain a sufficient number of COVID-19 IgG/IgM Rapid Test kits to meet demand if any, the demand or lack thereof for the COVID-19 IgG/IgM Rapid Test Kit,
On March 23, 2020, Aytu BioScience, Inc. (the “Company"), reported that it has received confirmation from the U.S. Food and Drug Administration (FDA) that the company may begin distribution of its Coronavirus Disease 2019 (“COVID-2019”) IgG/IgM Rapid Test throughout the United States. The COVID-19 IgG/IgM Rapid Test is intended for professional use and delivers results between 2 and 10 minutes at the point-of-care
On April 1, 2020, Aytu BioScience, Inc. (the “Company”) a specialty pharmaceutical company focused on commercializing novel products that address significant patient needs announced today that it has received its first Coronavirus Disease 2019 (“COVID-2019”) IgG/IgM Rapid Test shipment containing 100,000 tests from the manufacturer
on March 31, 2020. The Company is now in the process of relabeling the test kits to comply with Food and Drug Administration (FDA) requirements relating to labeling of COVID-19 serology test kits and expects to begin filling current backorders and additional incoming orders shortly thereafter.
So when aytu loses the eua then what? There is no doubt once they lose the eua they will be trading their normal 25 cents again. This was a short term play. Nothing left but dilution by those that bought high, shorts and the company. The run is over. Face it
Don't you mean 1.5, 1.4, 1.3 like things have been going. The price is baked in. Its already up 5x
At yesterday's 10 million and today's 12 that still makes for a slow week compared to the 450 million
Airplanes don't wait in customs but the cargo does. We already know these are clearing customs with the help of Colorado government
But everyone is excited over 12k shares today saying there's big volume