CytoSorbents to Present at Biotech Showcase™ 2020

On January 7, 2020 CytoSorbents Corporation (NASDAQ: CTSO), a critical care immunotherapy leader commercializing its CytoSorb blood purification technology to treat deadly inflammation in critically-ill and cardiac surgery patients around the world, reported that the Company will present an overview of the company at Biotech Showcase 2020 on Monday, January 13, 2020 in San Francisco, CA and meet with investors in 1×1 meetings throughout the day (Press release, Cytosorbents, JAN 7, 2020, View Source [SID1234552819]).

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Biotech Showcase 2020
Where: Hilton San Francisco Union Square, 333 O’Farrell Street, San Francisco, CA
When: Monday, January 13, 2020 from 3:00PM-3:30PM PST
Webcast: Biotech Showcase 2020 Webcast Link

A live webcast of the presentation will be available at the above webcast link. An archived replay of the webcast will be available for 90 days following the event.

Replimune to Present at the 38th Annual J.P.Morgan Healthcare Conference

On January 7, 2020 Replimune Group Inc. (NASDAQ: REPL), a biotechnology company developing oncolytic immuno-gene therapies derived from its Immulytic platform, reported that Robert Coffin, Ph.D., Chief Executive Officer and Director of Replimune, will present at the 38th Annual J.P.Morgan Healthcare Conference on Tuesday, January 14, 2020 at 5:00 PM PT at the Westin St. Francis Hotel in San Francisco, CA (Press release, Replimune, JAN 7, 2020, View Source [SID1234552786]).

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A simultaneous webcast will be available in the Investors section of Replimune’s website at www.replimune.com. A replay will be available for 30 days following the conference.

BioMarker Strategies Awarded Phase II National Cancer Institute Contract to Develop Novel Predictive Test for Response to Immunotherapies for Patients with Non-Small Cell Lung Cancer

On January 7, 2020 BioMarker Strategies, LLC, reported that the National Cancer Institute (NCI) has awarded the Company a Phase II Small Business Innovation Research (SBIR) contract to continue development of its PathMAP Immunotherapy test to predict clinical response to PD-1/PD-L1 targeted immune checkpoint inhibitors, both alone and in combination with chemotherapies, for individual patients with non-small cell lung cancer (NSCLC) (Press release, BioMarker Strategies, JAN 7, 2020, View Source [SID1234552802]). The contract totals $1.5 million over two years.

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The Phase II contract follows a Phase I contract that supported development of initial proof-of-concept data for PathMAP Immunotherapy as a pathway-based test to identify patients who could otherwise be excluded from treatment with these very important therapies, because currently available tests show them as negative for the biomarkers currently used to identify patients who might benefit.

"Durable responses have been observed in patients with non-small cell lung cancer who have received treatment with immune checkpoint inhibitors, which enable the immune system to kill tumors," said Jerry Parrott, President and CEO of BioMarker Strategies. "However, the reality is that the objective response rate to single-agent immunotherapy is low, at 10-30%. And, the emergence of resistance is observed in patients who initially respond, just as is observed with chemotherapies. This Phase II SBIR contract from NCI will enable us to continue development of our PathMAP Immunotherapy test to predict individual patient response to checkpoint inhibitors, both alone and in combination with chemotherapies."

This project is funded in whole or in part with Federal funds from the National Cancer Institute, National Institutes of Health, Department of Health and Human Services, under Contract No. 75N91019C00022.

Lung cancer is the leading cause of cancer death in the United States, with an estimated 154,000 deaths in 2018. NSCLC is responsible for more than 80% of these deaths.

TwinStrand Biosciences Accelerates Commercialization with $16M in Series A Funding

On January 7, 2020 TwinStrand Biosciences, a novel genetic sequencing technology company, reported the close of $16 million in Series A funding, including $12 million in new capital. Madrona Venture Group led the investment with participation from Alexandria Venture Investments, Ridgeback Capital and Sahsen Ventures (Press release, Twinstrand Therapeutics, JAN 7, 2020, View Source [SID1234552820]). The funding will be used to accelerate the company’s commercial pipeline, as well as to support the growth of corporate infrastructure and pharmaceutical partnerships. The University of Washington spinout previously raised $5.5 million in Seed funding, in addition to $6.4 million in SBIR grants, to develop and commercialize its Duplex Sequencing technology.

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Duplex Sequencing is a biochemistry and software-based enhancement to existing DNA sequencing platforms that enables researchers and clinicians to detect genetic "needles in a haystack." By identifying ultra-low frequency DNA mutations with a resolution 10,000-fold greater than conventional tools on the market, clinically important decisions can be made with confidence. Such sensitivity and specificity is vital for a range of applications, including early cancer detection, monitoring for residual cancer after treatment, genetic toxicology, and drug development, among others.

"We are able to directly observe genetic phenomena in ways that have simply never been possible before," said Dr. Jesse Salk, CEO, Chief Scientific Officer and Co-founder of TwinStrand. "For example, typically, it takes years of testing to show that new drugs are safe from the perspective of cancer risk, at a cost of millions in research and development. We can now achieve this in days or weeks, with the ultimate goal of getting important drugs to patients much sooner. Similarly, we have now shown that it is possible to detect unrecognized carcinogen exposures in people, and we hope to use this to both help affected patients get care and to aid public health authorities in finding and eliminating carcinogens in the environment."

Duplex Sequencing identifies extremely rare mutations that go undetected by current next-generation sequencing (NGS) platforms. TwinStrand’s scientist-leaders have authored more than 15 peer-reviewed articles on Duplex Sequencing and have developed a portfolio of over 45 patents and patent applications. The company is already collaborating with pharmaceutical companies, academic centers, clinical research networks, and federal regulatory agencies.

"Being able to read our DNA with the breakthrough accuracy of Duplex Sequencing will have a profound impact on each of our lives," said Terry Myerson, Venture Partner at Madrona Venture Group. "TwinStrand’s innovation is at the forefront of the intersection of life sciences and computer science. We are excited to invest in the incredible team and opportunity ahead at TwinStrand."

Vivoryon Therapeutics to Attend 38th Annual J.P. Morgan Healthcare Conference in January 2020

On January 7, 2020 Vivoryon Therapeutics AG (Euronext Amsterdam: VVY, ISIN DE0007921835), reported that the company is scheduled to attend the J.P. Morgan Healthcare Conference (Press release, Vivoryon Therapeutics, JAN 7, 2020, View Source [SID1234552770]).

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38th Annual JP Morgan Healthcare Conference – Biotech Showcase

Date: January 13-16, 2020

Venue: San Francisco, USA

Participant: Dr. Ulrich Dauer, CEO