After Scientific Breakthrough: Digid Seeks FDA Approval for Its Rapid Corona Antigen Test

Mainz, Germany, May 30, 2020 – (ACN Newswire) – At the high-security laboratory of the Helmholtz Centre for Infection Research (HZI) in Braunschweig, Germany, the revolutionary Cantisense(TM) technology of the German health technology company Digital Diagnostics AG was used for the first time to successfully detect SARS-CoV-2 viruses in high measuring accuracy in test liquids.



Figure 1: Point-of-care test kit: sensor hub, biosensor, mobile device. With digid's point-of-care solution, the measurement results are transmitted wirelessly from a sensor hub to a mobile device. By connecting to a secure analytics platform, the numerous sensor data can be augmented with further data and processed anonymously for research and diagnostic applications. (prototype/copyright: Digital Diagnostics AG)



In contrast to PCR testing, the new test provides a clear electronic "YES" or "NO" information within a few minutes, saving precious time in the diagnosis. What's more, the Digid Cantisense(TM) SARS-CoV-2 Test directly detects the presence of the virus while other rapid tests only recognize antibodies.

Konstantin Kloppstech, CTO at Digital Diagnostics, says: "Recent test series at the HZI high-security laboratory have shown that SARS-CoV-2 viruses can be detected directly using our Cantisense technology and without the need for PCR or further sample processing. This is a scientific breakthrough. We have coated cantilevers with a capture layer of highly specific monoclonal antibodies, which can reliably bind SARS-CO-2 viruses in the test fluid."

Constantin von Gersdorff, CEO of Digital Diagnostics, said: "The next step will be to initiate clinical studies with patient samples. To this end, we have already established international collaborations with leading hospitals."

With Digid's test kit, the measurement results are transmitted wirelessly from a sensor hub to a mobile device. By connecting to a secure analytics platform, the sensor data can be augmented with further data and processed anonymously for research and diagnostic applications.

Due to its measurement speed and the highly reliable results, the test is particularly suitable to support the containment of the current SARS-CoV-2 pandemic. The test offers the possibility of simple and rapid testing of patients and medical staff as an alternative to laboratory tests and enables reliable identification of infected persons within minutes. The possible areas of application therefore also include screening for access control at airports and railway stations, hospitals and specially protected areas (such as retirement homes) as well as for companies who want to ensure that their production runs smoothly and safely.

Digital Diagnostics has applied for approval of the Digid Cantisense(TM) SARS-CoV-2 Test by the US Food and Drug Administration (FDA). Digid aims to provide millions of units by July 2020. A further scaling of capacities is planned in the short term. The experts at Digital Diagnostics are also working at full speed to further develop the technology and to adapt the point-of-care testing procedure for use by consumers at home.

Press contact
Thomas Huber
semanticom GmbH
+49 30 275 80 81 11
digid-pr@semanticom.eu

Related Images
https://www.newsfilecorp.com/redirect/waAZCxPR
Point-of-care test kit: sensor hub, biosensor, mobile device
With digid's point-of-care solution, the measurement results are transmitted wirelessly from a sensor hub to a mobile device. By connecting to a secure analytics platform, the numerous sensor data can be augmented with further data and processed anonymously for research and diagnostic applications. (prototype/copyright: Digital Diagnostics AG)

Related Links
https://digid.com/en/

Copyright 2020 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Sino Biopharmaceutical Announces 2020 First Quarterly Results

HONG KONG, May 28, 2020 – (ACN Newswire) – Sino Biopharmaceutical Limited ("Sino Biopharmaceutical" or the "Company", together with its subsidiaries, the "Group") (HKEX:1177), a leading, innovative research and development ("R&D") driven pharmaceutical conglomerate in the PRC, has announced its unaudited first quarterly results for the three months ended 31 March 2020 ("the review period").

Results Highlights
– At the beginning of the COVID-19 pandemic, owing to its strong sense of social responsibility and in line with its mission, the Group took the initiative to donate RMB10 million to the Chinese Academy of Medical Sciences on 26 January to support research on COVID-19. At the same time, the Group has promptly set up an anti-pandemic supplies procurement team to purchase supplies, such as face masks, protective gloves, protective clothing, negative pressure isolation ambulances and diagnosis and treatment related products, from different countries for donating to anti-pandemic frontline medical workers. Up to the end of the period, Sino Biopharm and its subsidiaries donated cash and supplies on 18 different occasions with a total value of nearly RMB22 million to anti-pandemic efforts.

– "The Establishment and Application of Key Technology Systems on Emulsification in New Pharmaceutical Preparation," a research project reported by Beijing Tide, in cooperation with Peking University, has been honoured with "The 2019 National Science and Technology Progress Award – Second Prize". The Group is one of the few pharmaceutical enterprises to be feted in this way. The accolade is prestigious national recognition of Beijing Tide's research and development platform of emulsification for high-end preparations.

– Construction of "The Purun Bio-Medical's R&D and Production Project" of Jiangsu Purun Bio-Medical Co., Ltd., a wholly-owned subsidiary of NJCTT located at Nanjing Jiangbei New Materials High-Tech Park, has officially commenced after the groundbreaking ceremony. Occupying an area of about 300 mu, NJCTT's product R&D and production capabilities would be substantially strengthened after the project is completed.

– The Group has obtained approval from the United States Food and Drug Administration ("FDA") for its application filed for "Fulvestrant Injection". This is another advance for the Group to sell its products in the international markets after Tenofovir Disoproxil Fumarate tablets obtained marketing authorization in the European Union.

– During the pandemic, the intravenous therapy of Magnesium Isoglycyrrhizinate injection (brand name: Tianqingganmei) was included as a supportive treatment for patients with mild and common symptoms (without severe underlying illnesses) in the "Treatment Practices for the Mild and Common Cases of Novel Coronavirus Pneumonia (Second Edition)" jointly published by the offices of the National Health Commission and National Administration of Traditional Chinese Medicine.

– Five products including "Budesonide Suspension for Inhalation" (brand name: Tianqingsuchang), "Sitagliptin Phosphate Tablet" and "Dabigatran Etexilate Capsules" (two specifications) obtained approval for drug registration. Three of these products are the first generic drug of their kind in China and have potential to become blockbuster products.

Results
For the three months ended 31 March 2020, the Group recorded revenue of approximately RMB6.22 billion, representing an increase of approximately 0.2% over the same period last year. During the period, profit attributable to the owners of the parent was approximately RMB862 million, approximately 0.6% higher than that of the same period last year. Earnings per share were approximately RMB6.85 cents, 0.7% higher than that of the same period last year. The Group has maintained a strong financial position with cash and bank balances reaching approximately RMB16.12 billion at the period end (as at 31 December 2019: approximately RMB11.91 billion).

The Board of Directors declared a quarterly dividend of HK2 cents per share (2019 first quarter: HK2 cents).

Business Highlights
During the period under review, most outpatient and inpatient visits at hospitals dropped dramatically due to the pandemic. On-site academic activities and face-to-face exchanges with professional doctors were also adversely affected. The Group quickly reacted and fully utilized third-party online academic exchange platforms to maintain communication with general medical practitioners and patients, thereby strengthening its support to online academic activities. Particularly in the areas of respiratory, infection and oncology that have been less affected by the pandemic, intensive online academic exchanges and promotion activities have been launched. The Group has also supported volunteer medical consultations taking place through online hospital networks. The chronic disease management platform of the Group for respiratory, oncology, analgesic, and kidney illnesses that has been actively operating was also used to enhance the service and professional assistance provided to doctors and patients.

For the production, in response to the government's strategies, the Group has resumed its production and operations at the early stage with strict precautions for isolation and social distancing, with the first priority to ensure the supply of much-needed anti-infection and respiratory drugs for the therapy of those patients infected with COVID-19, as well as the oncology drugs with pressing demand. The respiratory medicine Tianqingsule (Tiotropium Bromide powder for inhalation); anti-infectious medicines Tianjie (Tigecycline for Injection), Fengruineng (Moxifloxacin Hydrochloride and Sodium Chloride Injection), Tianli (Linezolid and Glucose Injections), and Tianming (Caspofungin Acetate for Injection); analgesics Flurbiprofen cataplasm and Parecoxib Sodium for Injection; and orthopedic medicine Gaisanchun (Calcitriol) capsules also recorded strong growth.

The sales from oncology drugs recorded the highest growth among all. In addition to the rapid growth of Anlotinib Hydrochloride capsules, sales of two products: Qingkeshu (Abiraterone Acetate Tablets), and Jizhi (Gefitinib Tablets) rapidly expanded after they secured the bid for the extended centralized drug procurements by the government. Other oncology products Yinishu (Dasatinib) tablets, Qianping (Bortezomib for Injection) and Shoufu (Capecitabine) tablets also recorded strong growth, which further enlarged the sales contribution of the oncology drug lines to the Group.

The newly launched products also significantly boosted the sales growth. In addition to Qingkeshu, and Jizhi mentioned above, products that have been approved for launch also recorded satisfactory results, including cardiovascular medicine Anbeining (Apixaban Tablets), contrast agent Qingliming (Iodixanol Injection), the first generic oncology drug Leweixin (Bendamustine Hydrochloride for Injection), Weishou (Azacitidine for Injection, the first generic drug) and the first generic anti-rheumatic drug Taiyan (Tofacitinib Citrate Tablets).

For R&D, several strategic products with strong potential have secured production approvals during the period, and 4 of them have been designated as meeting the Consistency Evaluation requirements at the same time.

During the review period, the sales performance of the Group's major medicine types are outlined below:

Hepatitis medicines
– The sales of hepatitis medicines amounted to approximately RMB1,329.61 million, representing approximately 21.4% of the Group's revenue.

Oncology medicines
– The sales of oncology medicines amounted to approximately RMB1,984.40 million, representing approximately 31.9% of the Group's revenue.

Orthopedic medicines
– The sales of orthopedic medicines amounted to approximately RMB467.75 million, representing approximately 7.5% of the Group's revenue.

Anti-infectious medicines
– The sales of anti-infectious medicines amounted to approximately RMB416.01 million, representing approximately 6.7% of the Group's revenue.

Respiratory system medicines
– The sales of respiratory medicines amounted to approximately RMB334.41 million, representing approximately 5.4% of the Group's revenue.

Others
– Sales of other medicines amounted to approximately RMB1,689.69 million, representing approximately 27.1% of the Group's revenue.

R&D
The Group has continued to focus its R&D efforts on new hepatitis, oncology and respiratory system and cardio-cerebral medicines. During the first quarter, the Group was granted 14 clinical trial approvals, 6 production approvals, and 6 approvals for Consistency Evaluation, and made 9 clinical trial applications, 3 applications for Consistency Evaluation and 2 production applications. Cumulatively, a total of 437 pharmaceutical products had obtained clinical trial approval, or were under clinical trial or applying for production approval. Out of these, 30 were for hepatitis medicines, 189 for oncology medicines, 24 for respiratory system medicines, 24 for endocrine, 40 for cardio-cerebral medicines and 130 for other medicines.

Over the years, the Group has been placing high importance on R&D and innovation, as well as through collaboration and imitation, to raise both R&D standards and efficiency. Regarding R&D as the lifeblood of the Group's development, the Group continues to devote into more resources. For the three months ended 31 March 2020, the total R&D expenditure of approximately RMB994 million, which accounted for approximately 16.0% of the Group's revenue, was charged to the statement of profit or loss and capitalized in the statement of financial position respectively.

The Group also emphasizes on the protection of intellectual property rights. It encourages its enterprises to apply for patent applications as a means to enhance the Group's core competitiveness. During the first quarter, the Group has received 25 authorized patent notices (21 invention patents, 2 utility model patents and 2 apparel design patents) and filed 123 new patent applications (120 invention patents and 3 apparel design patents). Cumulatively, the Group has obtained 787 invention patent approvals, 25 utility model patents and 92 apparel design patents.

Prospects
The COVID-19 pandemic remains serious in regions outside China, which will continue to affect the economy. Through implementing effective prevention and control measures, the pandemic in China has essentially come under control and enterprises around the country have gradually resumed work and operation. The decline in economic indicators has also narrowed. Hence, China is expected to be among the first countries to leave the worst impact of the pandemic behind and return to normal production, everyday life and routine medical procedures. Pent-up demand for medical diagnosis and treatment limited by isolation during the pandemic period will gradually be unleashed, which might lead to the rapid growth for the pharmaceutical industry in the immediate future.

The nationwide implementation and extension of the centralized drug procurement programme in "4+7" cities has substantially squeezed the profit of selected drugs as well as many competitive generic drugs. The COVID-19 pandemic has weighed further on the operations of small- and medium-pharmaceutical companies with limited R&D capabilities and only a few new products. Some of them are even encountering difficulties in maintaining the viability of their business. As a result, the consolidation and elimination of the weaker players in the market will accelerate and developing and launching innovative and popular products have become the primary capabilities required by pharmaceutical enterprises if they wish to win amidst the fiercer market competition.

The Group's strong investment in R&D over the years has borne fruit, as evidenced by the maturing innovative platforms and optimization of creative talent structure for both small molecule and macro-molecule drugs. The continuous huge investment in R&D has also ensured that it can engage in the launch of new products every year, which has become and will continue to be the key growth driver for the Group's results.

Introduction of Newly Approved Products:
Tianqingsuchang (Budesonide Suspension for Inhalation): A glucocorticoid inhalant with strong anti-inflammatory properties used for first-line treatment of asthma. There are approximately 235 million asthma patients globally, and the number in China exceeds 45 million. The efficacy of nebulized inhalation suspension is more trusted by doctors and patients when compared to other dosage forms but needs to be administered under the supervision of medical professionals in hospitals.

Sitagliptin Phosphate Tablet: An effective and highly selective dipeptidyl peptidase-4 (DPP-4) inhibitor used for improving glycemic control in patients with type 2 diabetes mellitus. Clinical trials show its efficacy in lowering blood sugar, and it can be used alone with high safety and fair tolerance, without increasing the risk of hypoglycemia and causing gastrointestinal reactions. More importantly, it offers long-term protection of beta-cells in the pancreas, which can slow the progress of diabetes.

Dabigatran Etexilate Capsules: A new generation non-Vitamin K oral anticoagulant used for the prevention of stroke and systemic embolism in patients with non-valvular atrial fibrillation. It is the first new oral anticoagulant launched since Warfarin in 50 years, and is the first oral anticoagulant approved for long term indications, signifying a milestone in the global anticoagulant drug sector.

About Sino Biopharmaceutical Limited (HKEX:1177)
Sino Biopharmaceutical Limited is a leading, innovative R&D driven pharmaceutical conglomerate in the PRC. Its business encompasses a fully-integrated chain which covers an array of R&D platforms, a line-up of intelligent production and a strong sales system. The Group's products have gained a competitive foothold in various therapeutic categories with promising potentials, comprising a variety of biopharmaceutical and chemical medicines for treating tumors, liver diseases, respiratory system diseases, anti-infectious diseases and orthopedic diseases.

Sino Biopharm is a constituent stock of the following indices: MSCI Global Standard Indices – MSCI China Index, Hang Seng Index, Hang Seng Index – Commerce & Industry, Hang Seng Composite Index, Hang Seng Composite Industry Index – Consumer Goods, Hang Seng Composite LargeCap Index, Hang Seng Composite LargeCap & MidCap Index, Hang Seng China (Hong Kong-listed) 100 Index and Hang Seng Stock Connect Hong Kong Index. Sino Biopharm was ranked as one of "Asia's Fab 50 Companies" by Forbes Asia for three consecutive years in 2016, 2017 and 2018.


Copyright 2020 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Nature Publishes Preclinical Characterization and Primate Efficacy Data on Junshi Biosciences’ COVID-19 Neutralizing Antibodies

SHANGHAI, CHINA, May 27, 2020 – (ACN Newswire) – Junshi Biosciences (HKEX: 1877) a leading innovation-driven biopharmaceutical company dedicated to the discovery, development, and commercialization of novel therapies, today announced the publication of research results from the company's efforts to generate therapeutic COVID-19 neutralizing antibodies. The paper, titled "A human neutralizing MAb targeting the receptor binding site of SARS-CoV-2" (Shi et al. Nature), was published today in the journal Nature. Junshi and partner Eli Lilly and Company (NYSE: LLY) intend to file an IND and initiate clinical trials in the U.S. and China in the second quarter of 2020.

The article reports the identification and characterization of two specific human monoclonal antibodies (CA1 and CB6) isolated from a recovered COVID-19 patient. While both antibodies demonstrated substantial neutralization activity in vitro against SARS-CoV-2, CB6 exhibited superior neutralizing activities. CB6 reduced virus levels by about 3 logs in rhesus monkeys when administered one day after infection. When given one day before viral challenge, CB6 was able to keep viral load at no more than 103 RNA copies/ml, demonstrating strong prophylactic protection. Structural studies showed that CB6 recognizes epitopes in SARS-CoV-2 receptor binding domain that overlap with angiotensin converting enzyme 2 (ACE2)-binding sites, thereby directly obstructing virus/receptor interactions. The Fc portion of CB6 was modified to lower the risk of Fc mediated acute lung injury.

"We have successfully leveraged the Company's years of expertise with our fully integrated R&D antibody technology platform, conducting multiple parallel development tracks of candidate antibodies that were subsequently tested in vivo infection model by the Institute of Microbiology, Chinese Academy of Sciences," said Hui Feng, Ph.D., Junshi Biosciences' Chief Operating Officer. "One of these candidates, described in the Nature paper, demonstrated strong neutralizing activity against COVID-19. We expect to file an IND for this candidate in the second quarter in collaboration with our partner, Lilly. As part of our effort to contribute in the fight against this global pandemic, our Company has increased its research and development efforts, leveraging our strengths in the field of antibody discovery."

"Lilly is proud to have partnered with Junshi Biosciences to develop CB6 as a potential treatment for COVID-19. The fact that CB6 can protect rhesus monkeys from COVID-19 infection suggests a potential for prophylactic use in humans," said Daniel Skovronsky, M.D., Ph.D., Lilly's chief scientific officer and president of Lilly Research Laboratories. "We are moving as quickly as possible to test such a protective effect in patients at risk for COVID-19."

The paper can be accessed on the journal's website here.
https://www.nature.com/articles/s41586-020-2380-z

About Junshi Biosciences
Established in 2012, Junshi Biosciences is committed to developing first-in-class and best-in-class drugs through original innovation and becoming a pioneer in the area of translational medicine to provide patients with effective and affordable treatment options. On December 24, 2018, Junshi Biosciences was listed on the Main Board of the Stock Exchange of Hong Kong with the stock code: 1877.HK. The Company has established a diversified R&D pipeline comprising 21 drug candidates with therapeutic areas covering cancer, metabolic diseases, autoimmune diseases, neurologic diseases, and Infectious disease. Product types include monoclonal antibodies, fusion proteins, antibody-drug conjugates, and small molecule drugs. With a combined 33,000L fermentation capacity in two GMP-facilities at Shanghai and Suzhou, Junshi has established the manufacturing infrastructure to support commercialization and provide our partners and patients with high-quality products through a global supply chain network. For more information, please visit: http://junshipharma.com/en/Index.html

Contact Information
IR Team:
info@junshipharma.com
+ 86 021-2250 0300


Copyright 2020 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Novotech and Endpoints to present APAC Clinical Trial webinar series

SYDNEY, May 26, 2020 – (ACN Newswire) – Leading Asia-Pacific biotech specialist CRO Novotech will collaborate with Endpoints, the independent biotech news platform, for a series of webinars on the advantages of conducting clinical trials in the Asia-Pacific.

"Clinical Trial Continuity in Asia-Pacific during the COVID-19 Pandemic" will be broadcast on 8 June, 2020, to open the series. To register please visit Endpoints at : https://tinyurl.com/y9j9szuf.

Endpoints Founder & CEO Arsalan Arif will moderate the sessions with Novotech executives, key opinion leaders from the region and biotech sponsors with Asia Pacific experience, including:

– Yooni Kim, Executive Director, Asia Operations at Novotech
– Alejandro Ricart M.D. VP Clinical Development at TG Therapeutics
– Daniela Caiazza, Director Clinical Operations ANZ at Novotech
– Hannah Tarrant, Project Director at Novotech
– Kristyn Munro, Director, Business Development Operations at Novotech

Arsalan Arif said, "As we return to business under a pandemic, biotechs are looking to reliably conduct trials. Asia-Pacific is clearly a top destination and having the Novotech team share their first-hand experiences with sites, research teams, and sponsors in the region will be invaluable to subscribers reviewing their next trial locations."

Novotech CEO Dr. John Moller said "Many countries in Asia Pacific have managed the COVID-19 pandemic extremely effectively, and sites have adapted quickly to ensure trial continuity. This presents an opportunity for sponsors to shift their activity from the US and Europe to Asia to ensure their trials stay on track."

The webinar will discuss:
– The status of COVID 19 in the region and the factors that have driven the relatively low spread
– Regulatory guidance and acceptability of remote monitoring and decentralized clinical trials in Asia-Pacific
– Risk management strategies

The APAC region is highly attractive for biotechs running clinical studies, with a streamlined regulatory environment and advanced medical infrastructure. Novotech and GlobalData released new data showing biotech companies since March 1 initiating 10% more Asian-Pacific than North American trials, and fully twice as many APAC Phase 1 trials.

Novotech manages 200+ clinical trials and projects annually in the region, which boasts large patient populations and world best medical and research teams and facilities. Novotech has partnered with leading institutions throughout APAC giving clients unique access to top researchers, investigators and key opinion leaders.

About Novotech – https://novotech-cro.com

Novotech is internationally recognized as the leading regional full-service contract research organization (CRO) in Asia-Pacific. Novotech has been instrumental in the success of over a thousand Phase I – IV clinical trials for biotechnology companies. Novotech was established in 1996, with offices in 11 locations across the region, and site partnerships with major health institutions.

Novotech provides clinical development services across all clinical trial phases and therapeutic areas including: feasibility assessments; ethics committee and regulatory submissions, data management, statistical analysis, medical monitoring, safety services, central lab services, report write-up to ICH requirements, project and vendor management. Novotech obtained the ISO 27001 certification which is the best-known standard in the ISO family providing requirements for an Information Security Management System. Together with the ISO 9001 Quality Management system, Novotech aims at the highest IT security and quality standards for patients and biotechnology companies.

For RFP enquiries: Please fill out the form available at https://novotech-cro.com/talk-to-an-expert

Media contact:
David James, Novotech.
communications@novotech-cro.com
US:+415 951 3228, Asia:+65 3159 3427
https://www.novotech-cro.com


Copyright 2020 ACN Newswire. All rights reserved. http://www.acnnewswire.com

New Drug Application of Penpulimab Co-developed by Sino Biopharmaceutical and Akeso Accepted by the National Medical Products Administration

HONG KONG, May 26, 2020 – (ACN Newswire) – Sino Biopharmaceutical Limited ("the Group") (HKEX: 1177), a leading, innovative research and development ("R&D") driven pharmaceutical conglomerate in the PRC, has announced that the new drug application of the anti PD-1 monoclonal antibody drug (generic name: Penpulimab; R&D code: AK105) jointly developed and commercialized by the Group and Akeso, Inc. ("Akeso", HKEX:9926), a biopharmaceutical company committed to R&D, production and commercialization of affordable innovative antibody drugs for patients worldwide, has been accepted by the National Medical Products Administration of the PRC, for the treatment of patients with relapsed or refractory Classical Hodgkin's Lymphoma.

Classical Hodgkin Lymphoma (cHL) is a B-cell lymphoma, and is also one of the most common
malignancies among young people. It has a single modal age distribution in China with a peak at around 40 years of age . cHL is one of the few tumors that can be cured, and the most common therapy is chemotherapy plus radiotherapy, with the 5-year survival rate of patients as high as over 80%. Although the first-line chemotherapy has a high clinical cure rate, a considerable portion of patients are insensitive to chemotherapy and approximately 5% to 10% of patients do not respond to the initial treatment .

Professor Zhu Jun, Co-principal investigator of the lead unit Beijing Cancer Hospital is full of expectations for such a differentiated anti PD-1 monoclonal product and said, through bioengineering technology, Penpulimab completely eliminate the binding activity of Fc receptors and avoid the antibody-dependent cell-mediated cytotoxicity (ADCC) effect. At the same time, compared with other drugs available in the market working on the same target, it has a slower rate of antigen binding and dissociation, which makes the biological effect stronger and improves its anti-tumor activity.

Co-lead researcher Professor Song Yuqin, Director of Lymphoma Department at Peking University Cancer Hospital said, in clinical trial, Penpulimab was observed with gratifying therapeutic data and good safety. As a clinician, Professor Song hoped that Penpulimab can be launched to the market soon, which will benefit more patients and their families.

About Sino Biopharmaceutical Limited (HKEX: 1177)
Sino Biopharmaceutical Limited is a leading, innovative R&D driven pharmaceutical conglomerate in the PRC. Its business encompasses a fully-integrated chain which covers an array of R&D platforms, a line-up of intelligent production and a strong sales system. The Group's products have gained a competitive foothold in various therapeutic categories with promising potentials, comprising a variety of biopharmaceutical and chemical medicines for treating tumors, liver diseases, respiratory system diseases, anti-infectious diseases and orthopedic diseases.

Sino Biopharm is a constituent stock of the following indices: MSCI Global Standard Indices – MSCI China Index, Hang Seng Index, Hang Seng Index – Commerce & Industry, Hang Seng Composite Index, Hang Seng Composite Industry Index – Consumer Goods, Hang Seng Composite LargeCap Index, Hang Seng Composite LargeCap & MidCap Index, Hang Seng China (Hong Kong-listed) 100 Index and Hang Seng Stock Connect Hong Kong Index. Sino Biopharm was ranked as one of "Asia's Fab 50 Companies" by Forbes Asia for three consecutive years in 2016, 2017 and 2018.



Copyright 2020 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Strong Effectiveness of NanoViricides Drug Candidates Observed in an Animal Model of Infection by an ACE2-using Human Coronavirus

SHELTON, CT / ACCESSWIRE, May 20, 2020 – (ACN Newswire) – NanoViricides, Inc. (NYSE American: NNVC) (the "Company") a leader in the development of highly effective antiviral therapies based on a novel nanomedicines platform, announced today that strong effectiveness against infection by an ACE2-utilizing coronavirus in an animal model has been observed for the drug candidates it is developing against SARS-CoV-2 to treat COVID-19 spectrum of diseases.

NanoViricides is developing an animal model for coronavirus infection using hCoV-NL63 as a surrogate for SARS-CoV-2, the virus that causes COVID-19 disease. HCoV-NL63 is a circulating human coronavirus that causes a disease that is similar to SARS-CoV-2, but much milder. Both viruses utilize the same cell receptor, namely ACE2, to gain entry into the cell. Because it causes a mild disease, hCoV-NL63 can be used in BSL2 environments, and the Company believes it is a useful surrogate for development of therapeutics against SARS-CoV-2 infection.

In this lethal direct-lung-infection model, animals in all groups developed lung disease which later led to multi-organ failures, a clinical pathology resembling that of the SARS-CoV-2. Reduction in loss of body weight at day 7 was used as the primary indicator of drug effectiveness. Rats were infected directly into lungs with lethal amounts of hCoV-NL63 virus particles and then different groups were treated separately with five different nanoviricides drug candidates, remdesivir as a positive control, and the vehicle as a negative control. The treatment was intravenous by tail-vein injection once daily for five days, except in the case of remdesivir wherein it was by tail-vein injection twice daily.

Animals treated with the five different nanoviricides showed significantly reduced body weight loss. The body weight loss was only 3.9% for the best nanoviricide candidate, ranging to 11.2% for the potentially least effective one, as compared to 20% in the vehicle-treated control group, in female animals (n=5 in each group). Male animals treated with the same nanoviricides also showed significantly reduced body weight loss. The body weight loss in male animals was 8.0% for the best nanoviricide candidate and ranged up to 10.9% for the potentially least effective one, as compared to 25% in the vehicle-treated control group (n=5 in each group). In comparison, remdesivir treatment led to a body weight loss of 15.2% in females and 18.6% in males in this study (see below). Smaller numbers mean less loss in body weight compared to starting body weight in the group, and indicate greater drug effectiveness.

The strong effectiveness of nanoviricide drug candidates in this model is consistent with the effectiveness observed in cell culture studies against infection of both hCoV-NL63, which was used in this study, and hCoV-229E, another circulating coronavirus that uses a distinctly different receptor, namely APN.

Thus this study corroborates the previous cell-culture effectiveness reported by the Company and provides confidence to the Company that these nanoviricides drug candidates may be expected to result in a clinical candidate to be pursued in human clinical trials.

The Company believes the fact that these nanoviricides anti-coronavirus drug candidates are highly effective against two distinctly different coronaviruses that use different cellular receptors is very significant. Specifically, it provides a rational basis to scientists indicating that even if the SARS-CoV-2 coronavirus mutates, the nanoviricides can be expected to continue to remain effective.

Importantly, nanoviricides are designed to act by a novel mechanism of action, trapping the virus particle like the "Venus-fly-trap" flower does for insects. Antibodies, in contrast, only label the virus for other components of the immune system to take care of. It is well known that the immune system is not functioning properly at least in severe COVID-19 patients.

The Company believes that these nanoviricides drug candidates are potentially superior to favipravir, based on cell culture studies and may be superior to remdesivir based on the results of this study, however, a definite conclusion to that effect cannot be drawn. Oral favipravir and infusion of remdesivir are two anti-viral drugs in clinical trials for the treatment of COVID-19.

Prior to filing for human clinical trials, NanoViricides plans on conducting studies to further determine the effectiveness against SARS-CoV-2, perform drug development studies for safety/toxicology, and request a pre-IND Meeting with the US FDA for regulatory guidance.

Human coronavirus NL63 (hCoV-NL63) uses the same ACE2 receptor as the SARS-CoV-2 that causes CoVID-19. Both in terms of its clinical pathology, and its receptor usage, it is known to be very similar to SARS-CoV-2, except much milder. Therefore the Company believes hCoV-NL63 is a good surrogate model for therapeutics development against SARS-CoV-2. HCoV-NL63 can be studied in a BSL2 lab whereas SARS-CoV-2 currently requires a BSL3 or BSL4 facility.

The striking difference in weight loss between the two sexes in this animal model was remarkable. It has been widely reported that men are more likely to suffer severe infection and fatalities from SARS-CoV-2 than women in the current pandemic. This feature was replicated in our animal model study indicating that biological sex differences are the driver of the differences in the severity of infection by the coronaviruses that utilize the ACE2 receptor.

The various receptors used by different coronaviruses appear to fall in the broad family of membrane-associated serine proteases. As a family, they share several structural features. Their substrate specificities are dictated by specific amino acid residues and their positions. However, the coronaviruses do not appear to insert into the specific substrate sites on their receptors as can be broadly deduced from limited, available knowledge of these interactions. NanoViricides believes that this has made it possible for the Company to develop receptor-mimetic virus-binding ligands that have broad-spectrum effectiveness against multiple coronaviruses that use different receptors.

HCoV-NL63 is known to cause severe lower respiratory tract infections in young children leading to hospitalization. The symptoms are generally less severe than SARS-CoV-2 but are similar. In most cases, hCoV-NL63 causes relatively mild disease, often associated with croup, bronchiolitis, and lower respiratory tract disease in children, and is considered to cause some of the common colds in adults. Thus, the clinical manifestation of hCoV-NL63 infection in pediatric patients is similar to that of SARS-CoV-2, although much less severe. SARS-CoV-2 causes clinically similar milder forms of disease in most patients, but moderate to severe disease requiring hospitalizations in about 15-20% of infected persons. These similarities imply that hCoV-NL63 should be a reasonable model virus for antiviral cell culture and animal studies in BSL2 environment in the course of antiviral drug development for SARS-CoV-2.

About NanoViricides

NanoViricides, Inc. (www.nanoviricides.com) is a development stage company that is creating special purpose nanomaterials for antiviral therapy. The Company's novel nanoviricide(R) class of drug candidates are designed to specifically attack enveloped virus particles and to dismantle them. Our lead drug candidate is NV-HHV-101 with its first indication as dermal topical cream for the treatment of shingles rash. The Company is also developing drugs against a number of viral diseases including oral and genital Herpes, viral diseases of the eye including EKC and herpes keratitis, H1N1 swine flu, H5N1 bird flu, seasonal Influenza, HIV, Hepatitis C, Rabies, Dengue fever, and Ebola virus, among others. The Company's technology is based on broad, exclusive, sub-licensable, field licenses to drugs developed in these areas from TheraCour Pharma, Inc. The Company does not currently have a license to the coronavirus field, however, TheraCour has not denied any licenses to the Company. The Company typically begins the licensing process only after demonstrating effectiveness of some candidates in optimization stage.

This press release contains forward-looking statements that reflect the Company's current expectation regarding future events. Actual events could differ materially and substantially from those projected herein and depend on a number of factors. Certain statements in this release, and other written or oral statements made by NanoViricides, Inc. are "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. You should not place undue reliance on forward-looking statements since they involve known and unknown risks, uncertainties and other factors which are, in some cases, beyond the Company's control and which could, and likely will, materially affect actual results, levels of activity, performance or achievements. The Company assumes no obligation to publicly update or revise these forward-looking statements for any reason, or to update the reasons actual results could differ materially from those anticipated in these forward-looking statements, even if new information becomes available in the future. Important factors that could cause actual results to differ materially from the company's expectations include, but are not limited to, those factors that are disclosed under the heading "Risk Factors" and elsewhere in documents filed by the company from time to time with the United States Securities and Exchange Commission and other regulatory authorities. Although it is not possible to predict or identify all such factors, they may include the following: demonstration and proof of principle in preclinical trials that a nanoviricide is safe and effective; successful development of our product candidates; our ability to seek and obtain regulatory approvals, including with respect to the indications we are seeking; the successful commercialization of our product candidates; and market acceptance of our products.

As with any drug development efforts, there can be no assurance that any of these candidates would show sufficient effectiveness and safety for human clinical development at this time.

There can be no assurance that the Company will be successful in establishing the necessary collaborations, although the Company has been successful at establishing necessary collaborations for its drug programs in the past.

FDA refers to US Food and Drug Administration. IND application refers to "Investigational New Drug" application. CMC refers to "Chemistry, Manufacture, and Controls".

Contact:
NanoViricides, Inc.
info@nanoviricides.com

Public Relations Contact:
MJ Clyburn
TraDigital IR
clyburn@tradigitalir.com

SOURCE: NanoViricides, Inc.

Copyright 2020 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Agilex Biolabs Presents the Australian Advantage, including the World’s Largest Rebate on Clinical Trial Spend, at BIO Korea 2020

SEOUL, KOREA, May 20, 2020 – (ACN Newswire) – Agilex Biolabs, Australia's largest specialist bioanalytical laboratory for biotech clinical trials, is presenting the Australian Advantage including the world's most attractive rebate on clinical trials costs, at BIO Korea 2020.

The presentation by Kurt Sales (B.Sc; B.Sc (MED) Hons; M.Sc, Ph.D, PGCM)
Director, Immunoassay at Agilex Biolabs, also detailed how well the Australian clinical trials industry had managed during the COVID-19 crisis with most sites, CROs, and labs including Agilex Biolabs, staying open.

The presentation is at 13.50 on Friday 22, May 2020 via the virtual conference platform. https://www.biokorea.org/index.asp

Agilex Biolabs also launched a News Video Update on the COVID-19 impact on clinical trials in Australia. Watch here. https://youtu.be/vZuHAYZ-GiE

Agilex Biolabs specializes in bioanalysis of small molecules and biologics for PK, immunogenicity, biomarkers and immunological pharmacodynamics assessments.

Agilex Biolabs, the only FDA-inspected lab of its type in the region, is located in Adelaide, South Australia in a science and biotech specialist hub.

Agilex Biolabs CEO Jason Valentine said: "Aglilex Biolabs has just expand its labs by more than 30% to accommodate biotech demand from APAC and the USA."

He said more than 38% of Agilex Biolabs' biotech clients already come from the APAC region – primarily from China and South Korea.

"APAC clients are particularly attracted by Agilex Biolabs' FDA-inspected status, and the more than 40% rebate on clinical trial spend that applies in Australia," he said.

"Our world-class bioanalytical facilities have OECD GLP Recognition with NATA (Australian Government OECD GLP Compliance monitoring authority) and ISO 17025 Accreditation for global recognition."

Agilex Biolabs specialises in bioanalysis of small molecules and biologics for PK, immunogenicity, biomarkers and immunological pharmacodynamics assessments utilising LC-MS/MS, immunoassay (Mesoscale, Gurolab, Luminex) and flow cytometry (BD FACSymphony A3, 20 colour cell analyser).

Agilex also offers pharmacodynamics services that include immunobiology services using the latest state-of-the-art technology to support immunology, cell biology and mode of action assays, including:
– Immunophenotyping
– Receptor occupancy
– Cytokine release assays (whole blood or PBMC stimulation assays) and cytokine/biomarker profiling
– PBMC assays and cellular mechanism of action assays (eg: ADCC)

The FDA-inspected facilities have more than 65 dedicated laboratory staff, and annually support more than 80 clinical trials. This year they will analyse more than 60,000 samples for pharma/biotechs from US, Europe and APAC.

Please Book a Briefing with us before you start your next clinical trial. https://calendly.com/agilexbiolabs/15min

Australia: +61 8 8302 8777 | China: +86 21 8036 9483 | South Korea: +82 80 812 1255 | USA: +1 800 247 1909

About Agilex Biolabs https://www.agilexbiolabs.com/

Agilex Biolabs, Australia's leading bioanalytical laboratory, has more than 20 years' experience in performing regulated bioanalysis, including quality method development, method validation and sample analysis services. We have successfully supported hundreds of preclinical and clinical trials around the world where customers choose Australia for the streamlined regulatory process and access to the world's most attractive R&D rebate of more than 40% on clinical trial work conducted in Australia.

We offer services for both small molecules and biologics for PK, immunogenicity (PD) and biomarker bioanalysis utilising the two platforms of LC-MS/MS and Immunoassay.

Agilex Biolabs operates a fully quality-assured laboratory ensuring that, within the principles of GLP, assays are validated to the latest FDA/EMA guidance and study samples are assayed and reported to the sponsor's desired format using WATSON LIMS. Laboratory certifications include OECD GLP and ISO/IEC17025.

Our highly experienced team consists of over 65 dedicated laboratory staff with over 15 years average industry experience across senior scientists. Expertise includes development of robust compliant PK and PD assays de novo or by method transfer.

Our laboratory is fitted with 7 SCIEX tandem mass spectrometers, 6 API 4000 and 1 QTRAP 5500 as our standard platform for LC-MS/MS analysis. For immunoassay, we employ the state-of-the-art systems of Meso Scale Discovery (MSD) and Gyrolab xPlore.

Agilex Biolabs owns a suite of validated biosimilar assays that have already supported biosimilar studies executed in the region. These assays include Avastin/Bevacizumab, Lucentis/Ranibizumab, Actemra/Tocilizumab, Xolair/Omalizumab, Herceptin/Trastuzumab and Solaris/Eculizumab. We would like to discuss how we can support companies with biosimilar pipelines looking to conduct trials in the region. Our validated biosimilar assays require less setup saving time and money.

Agilex Biolabs also have a suite of biomarker assays that have been developed to support studies in the areas of endocrinology (estrone, estradiol, progesterone, testosterone and others).

Recently, Agilex Biolabs has added a comprehensive cannabinoid assay to its suite of validated assays to support clinical trials. The fully validated assay includes the five cannabinoids THC, CBD, CBN and the two THC-metabolites OHTHC and COOHTHC.

Our LC-MS/MS experience includes NCEs, sugars, nucleotides, enantiomers, steroids, prodrugs, peptides, immunosuppressants, nanoparticles, neurotransmitters, oligonucleotides and polymeric mixtures.

Our biologics experience entails PK analysis using colorimetric, fluorescence or chemiluminescence detection for recombinant or fusion proteins, monoclonal antibodies, ADCs, immunogenicity testing, biomarker analysis and PBMC blood stimulation assays.

See us featured in Endpoints https://tinyurl.com/uqmkzcu

Media Contact:
Kate Newton
Media@AgilexBiolabs.com

Copyright 2020 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Results from Clinical Trials of Penpulimab in Combination with Anlotinib for 1L HCC Co-developed by Sino Biopharmaceutical and Akeso Accepted for Presentation at ASCO Annual Meeting

HONG KONG, May 19, 2020 – (ACN Newswire) – Sino Biopharmaceutical Limited (HKEX: 1177), a leading, innovative research and development ("R&D") driven pharmaceutical conglomerate in the PRC, has announced that the abstracts on phase II study on clinical efficacy and safety of Penpulimab (AK105, PD-1 monoclonal antibody) it jointly developed and commercialized with Akeso, Inc. ("Akeso", HKEX:9926) in combination with Anlotinib for first-line treatment of advanced hepatocellular carcinoma ("1L HCC"), have been accepted for poster presentation at the upcoming 2020 American Society of Clinical Oncology ("ASCO") Annual Meeting.

As of to date, various phase II/III studies on combination of Penpulimab with Anlotinib have been activated, regarding treatment of various major tumors including: squamous non-small cell lung cancer, gastric cancer, esophageal squamous cell carcinoma, HCC, urothelial cancer, head and neck cancer, MSI-H or dMMR solid tumor and neuroendocrine carcinoma.

Prof. Shunchang Jiao, Director of Oncology Department of General Hospital of People's Liberation Army, also the leading Principal Investigator for this study, said, "The current option for treating unresectable HCC are mainly sorafenib and recently approved lenvatinib. The overall survival for levatinib was similar to that of sorafenib and the overall survival rate at 6 months for sorafenib was 72.2% . Anti-PD-1 Penpulimab in combination with lower dose of anti-angiogenic inhibitor Anlotinib shows encouraging early efficacy results and good safety profile for unresectable HCC. The DCR reached 84% and the overall survival rate at 6 months reached 91.6% which apparently was a great improvement on clinical efficacy. This combination therapy had a manageable safety profile, and had a potential safety advantage as compared with other combination therapies of immunotherapy and anti-angiogenic inhibitor. The preliminary results from this study suggest that Penpulimab with higher dose of Anlotinib may further improve the clinical efficacy for unresectable HCC patients. As a clinician, I look forward to bringing better treatment options for HCC patients in the near future."

Dr. Jia Fan, Academician, Director of Fudan University affiliated Zhongshan Hospital, said, "Clinical results from a phase II study of anti-PD-1 Penpulimab in combination with anti-angiogenic inhibitor Anlotinib as first-line therapy for unresectable HCC to be released on the coming ASCO20 show that the combination therapy had a manageable safety profile and encouraging antitumor activities. Based on the preliminary data of this study, the evaluation of Penpulimab in combination with Anlotinib in a phase III study for first-line HCC versus sorafenib is currently underway. Co-leading sites Fudan University affiliated Zhongshan Hospital and General Hospital of People's Liberation Army along with more than 60 other sites across the country participated in this study.

HCC, one of the most dominating malignant tumors in China, a barricade to invade, still needs more efforts on diagnosis and treatment. The rise of China-based innovative drug discovery and development is strongly promoting the continuous advances in HCC treatment in China. The combination therapy of Penpulimab, an anti-PD-1 antibody with key differentiating features, and the novel small molecule anti-angiogenic inhibitor of multi-targets Anlotinib is expected to become one of the essential first-line treatment options for HCC."

Akeso is a biopharmaceutical company committed to R&D, production and commercialization of affordable innovative antibody drugs for patients worldwide. The ASCO Annual Meeting is one of the largest and most authoritative clinical oncology conferences in the world where top oncology experts worldwide gather to discuss the results of recent clinical oncology studies and the latest oncology treatment technologies. Many of these professionals select this conference to first announce important discoveries and clinical trial results.

About Sino Biopharmaceutical Limited (HKEX:1177)
Sino Biopharmaceutical Limited is a leading, innovative R&D driven pharmaceutical conglomerate in the PRC. Its business encompasses a fully-integrated chain which covers an array of R&D platforms, a line-up of intelligent production and a strong sales system. The Group's products have gained a competitive foothold in various therapeutic categories with promising potentials, comprising a variety of biopharmaceutical and chemical medicines for treating liver diseases, tumors, cardio-cerebral diseases, orthopedic diseases, digestive system diseases, infections and respiratory system diseases.

Sino Biopharm is a constituent stock of the following indices: MSCI Global Standard Indices – MSCI China Index, Hang Seng Index, Hang Seng Index – Commerce & Industry, Hang Seng Composite Index, Hang Seng Composite Industry Index – Consumer Goods, Hang Seng Composite LargeCap Index, Hang Seng Composite LargeCap & MidCap Index, Hang Seng China (Hong Kong-listed) 100 Index and Hang Seng Stock Connect Hong Kong Index. Sino Biopharm was ranked as one of "Asia's Fab 50 Companies" by Forbes Asia for three consecutive years in 2016, 2017 and 2018.


Copyright 2020 ACN Newswire. All rights reserved. http://www.acnnewswire.com

BIO Asia-Taiwan 2020 Online + Live: Finding Cures in the Crisis

TAIPEI, May 13, 2020 – (ACN Newswire) – Taiwan BIO (Bio Industry Organization) together with BIO (the global Biotechnology Innovation Organization) announced May 7 that BIO Asia-Taiwan 2020 would go ahead as scheduled with a new online and live model; BIO Asia-Taiwan 2020 Online + Live. This event will be the first and biggest major industry gathering in Asia since the onset of this global pandemic crisis. With a blockbuster line up of speakers and presenting companies, this exciting event is expected to attract more than 2,000 professionals from 600 companies from around the world, and host more than 3,500 one-on-one business meetings. With the biomedical industry at the frontline driving discoveries and developments to combat the pandemic, opportunities are ripe for partnering, raising funds, and making deals.



(From left to right) William Foreman, AmCham President; Chen Chi-Mai, Vice Premier of Executive Yuan; Johnsee Lee, Chairman, Taiwan Bio Industry Organization; Shieh Dar-Bin, Deputy Minister, Ministry of Science and Technology



Johnsee Lee, Chairman of the Organizing Committee for BIO Asia-Taiwan 2020 Online + Live announced that the theme of this year's convention fittingly for these times was 'Finding Cures in the Crisis'. "With the pandemic sweeping the world, the biotechnology industry is more important than ever, and must keep innovating and working hard. But with countries and cities isolated, this makes the deal making and international partnering – defining characteristics of this industry – extremely difficult, just when the world needs us the most. The Organizing Committee has decided that with this need, it was important to go ahead with BIO Asia-Taiwan as scheduled 22-26 July, but with activities held online with an 'online + live' approach.

Vice Premier of the Executive Yuan Chen Chi-Mai commented that BIO Asia-Taiwan 2020 is an excellent opportunity for Taiwan's burgeoning biomedical industry to link up to the international bio-community, even more so during these times. "I hope that through this event the world will witness the efforts and success highlights of Taiwan's pandemic response."

James C. Greenwood, President and CEO, Biotechnology Innovation Organization (BIO) in a pre-recorded message expressed his full support for the gathering in its new format and recognized Taiwan's handling of the pandemic.

Minister of Health and Welfare Chen Shih-Chung, although unable to attend in person, also expressed his support for the event in a recorded message, and invited biomedical professionals from around the world to take part in the July occasion.

Deputy Minister of Science and Technology Shieh Dar-Bin, in his remarks said that he is very much looking forward to the presenting the achievements of the cooperation between Taiwan's academic and research communities, and industry.

BIO Asia-Taiwan 2020 Online + Live will again include forums and seminars, an exhibition, partnering meetings, and company presentations; this time in online formats. With this new model an even higher caliber line-up of international speakers is expected. On-site opening and awards ceremonies will be held live and accessible online in real time. If the pandemic situation allows, the exhibition hall will be open with strong infection-prevention measures in place. In addition, a free online biomedical education forum program will be newly added this year, allowing more people the opportunity to participate.

It is worth noting that the BIO One-on-One Partnering(TM) platform hosted more than 2,000 meetings at BIO Asia-Taiwan last year, and this year, through 24-hour accessibility and no geographical restrictions, we expect even greater meeting numbers and even more participation from overseas companies and investors. The Online Company Presentation program will provide outlook and growth briefing opportunities to boost companies onto the world stage. In addition, the Online Exhibition will not only allow for strong visibility of a company or organization, but also provide interactive visitor engagement opportunities such as exchanging business cards, forming chat groups or rooms, and so on. And visitors can join our Online Lounge and take part in social media-type activities to facilitate and replicate the social and networking elements so important to the conference experience.

BIO Asia-Taiwan 2020 Online + Live will focus on five topics: Combating the Pandemic, Precision Medicine, Advanced Therapies, Investment & Collaboration, and Digital Health. With the strong pandemic focus, Johnsee Lee said, "We plan to invite representatives of the World Health Organization (WHO) as well as global and Asian pandemic experts to share their experiences and discuss the latest developments in rapid diagnostics, therapeutics and vaccines."

Johnsee Lee, in concluding the event, expressed his hope that BIO Asia-Taiwan 2020 through its new 'online + live' format will be a unique and exciting occasion, and showcase not only Taiwan's renown pandemic prevention efforts but also its growing advantage in this sector and spotlight biotech, pharmaceutical, medical devices, precision medicine advances, as well as AI applications, ICT and IoT technologies. "We hope this event will encourage Taiwanese companies to enter the global market, and help upgrade the development of the local biotechnology industry."

Registration for the conference is now open. Please visit the website at www.bioasiataiwan.com

Contact:
Daisy Tsai
E-mail: daisy@taiwanbio.org.tw

Copyright 2020 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Cyber Company to Supply 50M Health “COVI-PASS(TM)”

LONDON, UK / ACCESSWIRE, May 8, 2020 – (ACN Newswire) – International Digital Health Technology firm Circle Pass Enterprises (CPE) has signed a deal with VST Enterprises Ltd (VSTE) the British cyber security company founded by tech entrepreneur Louis-James Davis (31) to integrate its state-of-the-art VCode(R) & VPlatform(R) technologies into the COVI-PASS(TM) Digital Health Passport.







Louis-James Davis CEO VST Enterprises



Powered by VST Enterprises groundbreaking cyber security technology VCode(R) & VPlatform(R), Circle Pass Enterprises has contracted with VST Enterprises for a fully secure Digital Health Passport – COVI-PASS(TM), to be paired with approved testing kits. CPE is to start shipping orders from next week for the first phased release of 50M COVI-PASS(TM) Digital Health Passports to both the private sector and Governments in over 15 countries, including Italy, Portugal, France, Panama, India, the US, Canada, Sweden, Spain, South Africa, Mexico, United Arab Emirates and The Netherlands.

The COVI-PASS(TM) Digital Health Passport works on an intelligent colour mapping system (green, amber, red) to authenticate and validate a COVID-19 test providing test history and relevant health information. This allows for accurate data metrics to assess those who have tested positive and negative and the location only of their testing. The COVI-PASS(TM) Digital Health Passport can be used as an authenticated gateway for Public Services, Businesses and Employees to manage a safe return to work, life, and safe travel.

Commenting on the deal VST Enterprises CEO Louis-James Davis said; "We are delighted to be working with CPE to supply our VCode(R) & VPlatform(R) technology and Digital Health Passport to create COVI-PASS(TM). It is also very encouraging that so many Governments and Enterprises across the world are engaging and using the COVI-PASS(TM) Health Passport and approved testing kits.

We firmly believe that the digital Health Passport alongside Government approved testing kits is the key to removing the lockdown restrictions in a gradual and controlled way. The current technology being trialed using bluetooth and proximity apps is fundamentally flawed because of its privacy issues of real time tracking, the security and data breaches which we are already seeing and being reported and the reticence for citizens to uptake and download the tracing app."

The Manchester based company are also in advanced discussions with senior UK Government officials, NHSX the technology arm of the NHS and the Home Office about its cyber security technology. The cyber security technology developed by VSTE can be used by various sectors including critical care workers doctors, nurses and health workers in the NHS and blue light emergency services key workers. Using a VCode(R) integrated with a health passport would help get them back on the front line in a safe and controlled manner.

Circle Pass Enterprises COO and Co Founder Adam Palmer said; "We are delighted to be working with Louis-James Davis and VST Enterprises to utilise the ground breaking cyber security technology of VCode(R) & VPlatform(R) to create COVI-PASS(TM) and to help tackle this global pandemic. One of the many unique features of the VCode(R) cyber security is that the VCode(R) technology can be scanned from up to 100 metres ensuring its social distancing compliance is robust and making it the only choice for a safe and secure digital health passport.

We are seeing unprecedented levels of interest from Governments, Businesses and major sporting organisations for the COVI-PASS(TM) solution. Due to the secure patented technology of the VCode(R) & VPlatform(R) – its ease of use and rapid implementation globally across all sectors – it is clear that COVI-PASS(TM) is the only viable solution for a safe return to work, life and travel protocols. Unlike Bluetooth, QR, or similar proximity apps, COVI-PASS(TM) using the VCode(R) & VPlatform(R) cyber security tech does not violate privacy issues of the user."

VSTE are also providing its VCode(R) & VPlatform(R) technology to work with the UNITED NATIONS as part of their SDG Collaboratory (Sustainable Development Goals) program – to provide a wide range of technology services to 9 Billion people by 2030 and which will be announced in the coming weeks.

VSTE and its partner REDSTRIKE the sports marketing agency are also in advanced discussions with major global sporting organisations and regulatory bodies in F1, motorsport, football, rugby, athletics, cycling, golf, tennis and basketball, to use its VCode(R) technology to help kick start the global sports economy.

REDSTRIKE MD Mike Farnan – the former Manchester United FC International MD – and his team have been pivotal in opening up high level talks with global sporting organisations.

The "COVI-PASS(TM)" Health Passport User Journey

A short infomercial explains the technology at www.covipass.com
– The user downloads the app to their smartphone device and onboards their key information such as name, address, age and verifies their identity using biometric fingerprint or facial scan.
– The user then takes the COVID-19 test which is administered by an authorised Health Care Professional, Nurse or Doctor. The test is geo fenced to that location and the test results are then scanned from the testing kit into the COVI-PASS(TM) Health Passport.
– A traffic light system then confirms their health status as either red or green, red for positive and green for negative. The amber colour indicates a countdown timer to when another test would be due and required.
– The user can then show the COVI-PASS(TM) health passport to authenticate their health status. The health passport can also be scanned well outside the safe distancing zone of 2/3m (and beyond) while the person is moving and at various angles to ensure continued social distancing guidelines.

VST Enterprises CEO Louis-James Davis added; "The issue at present with other health passports is that not only is the feed of information voluntary, but the technology being used (in most cases a QR code or barcode) can't be interacted with outside of the safe distancing zone. Data and sensitive information scanned or stored in either a QR code and barcode can be hacked and are inherently insecure, leaving data and personal details to be compromised. Both barcodes and QR codes are old second generation technology. VCode(R) & VPlatform(R) represent the next "third generation" of ultra secure and versatile code technology to military grade encryption with over 2 Quintillion code permutations.

The technology used in contact tracing and Bluetooth proximity apps currently being used by various Governments is fundamentally flawed. Not only can the bluetooth app and its data be compromised and hacked, but it can also lead to false flag data. There are also real fundamental issues of privacy, and being tracked in real time which most citizens will resist at all levels. This will also contribute to anxiety about the technology thus resulting in poor uptake. Without 100% uptake of the population using the technology its data is ineffective, and does not give a true picture of the virus tracing. Add into this the fact that bluetooth can also penetrate glass and walls. So someone for example, who is self isolating in a house that has tested positive for COVID-19 would give off a false flag to someone walking past their house who has tested negative, that they had been in proximity to someone who has tested positive."

NOTES TO EDITORS

About VST Enterprises Ltd

VST Enterprises (VSTE) is the company behind the VCode(R) and VPlatform(R). Headquartered in Manchester, the company has satellite offices around the world and is operational in 16 countries.

About VCode(R) & VPlatform(R)

VCode(R) represents the next generation of code scanning technology – an evolutionary step forward from traditional barcodes and QR Codes. VCode(R) has an infinite range of applications and capabilities from secure identification and ID, to geo location and geo fencing, asset tracking, authentication and permission based authorisations, fan and customer engagement through to biometrics and facial recognition.

VCode(R) can be used across a wide range of applications to securely purchase music, video and film content to concert and sports event tickets. It can also be used to screen exclusive film content, sales promotion and marketing and create dynamic marketing and fan engagement campaigns. Its wider uses also include anti counterfeiting and anti piracy.

A VCode(R) can be scanned from over 100 metres, with a 80:1 distance to size scan ratio, at 170-degree angles, on and from moving objects, and upon any multimedia or television screen and even when the VCode(R) is microscopic on bank notes or minerals. This allows users to access exclusive content, check the validity and authenticity of an item and make purchases while on the move. VCode(R) provides military grade encryption with over 2.2 Quintillion combination codes.

Supporting the VCode(R) app is the VPlatform(R) – a secure cloud based portal that allows users to create VCode(R) and manage the content they lead to. The VPlatform(R) also provides users with real time analytics on who scanned their codes, when and where the scans took place, providing vital consumer data.

The VPlatform(R) enables push notifications and rewards to be sent back to individuals who have made VCode(R) scans, offering opportunities for brands to significantly enhance their engagement levels with their client base. For more information please visit www.vstenterprises.com or www.vcode.it/developers

About Circle Pass Enterprises (COVI-PASS(TM))

Circle Pass Enterprises (CPE) is a global Digital Health Technology Company. Circle Pass Enterprises, which owns COVI-PASS(TM), has offices in London, Dublin, Amsterdam, Dubai, New York, Hong Kong and Chennai. Supported by a number of leading scientists and medical professionals, the CPE executive leadership team are developing digital Health Technology solutions for global application. For more information please visit www.covipass.com

For further information and all press and media enquiries on VCode(R) & VPlatform(R) VST Enterprises Ltd
Please contact Gerard Franklin – Head Of Communications & External Relations
M: 07885 388398 e: gerard@vstenterprises.com
VST Enterprises Ltd | The Lexicon | Mount Street | Manchester | M2 5NT

SOURCE: VST Enterprises Ltd

Copyright 2020 ACN Newswire. All rights reserved. http://www.acnnewswire.com