Molecular Templates to Participate in Upcoming Virtual Investor Conferences

On November 16, 2020 Molecular Templates, Inc. (Nasdaq: MTEM, "Molecular Templates" or "MTEM"), a clinical-stage biopharmaceutical company focused on the discovery and development of the company’s proprietary engineered toxin bodies (ETBs), which are differentiated, targeted, biologic therapeutics for cancer and other serious diseases, reported that it will deliver presentations and participate in 1on1 meetings at the Stifel 2020 Virtual Healthcare Conference and the 3rd Annual Evercore ISI HealthCONx Conference (Press release, Molecular Templates, NOV 16, 2020, View Source [SID1234571142]). In addition, management will be available for virtual 1on1 meetings at the Jefferies Virtual London Healthcare Conference.

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Stifel 2020 Virtual Healthcare Conference
Conference Dates: November 16-18
Presentation Date and Time: November 17 at 9:20am ET

Jefferies Virtual London Healthcare Conference
Conference Dates: November 17 – 19
Available for 1on1 meetings

3rd Annual Evercore ISI HealthCONx Conference
Conference Dates: December 1-3
Presentation Date and Time: December 3 at 10:05am ET
Live webcasts of the Stifel and Evercore ISI presentations will be available in the "News and Events" section of the MTEM website at www.mtem.com. Additionally, replays of the webcasts will be available on the corporate website following the conferences.

Susan G. Komen®, Inflammatory Breast Cancer (IBC) Research Foundation and Milburn Foundation® Raise Nearly $1 Million for IBC Research, Critical Breast Cancer Programs

On November 16, 2020 A partnership between Susan G. Komen, the Inflammatory Breast Cancer (IBC) Research Foundation and the Milburn Foundation reported that it has raised nearly $1 million for more research into inflammatory breast cancer – an aggressive subtype of breast cancer that is challenging to diagnose and treat – and other important programs (Press release, Susan G Komen, NOV 16, 2020, View Source [SID1234571163]).

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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IBC can be missed on a mammogram because it usually doesn’t present as a lump in the breast. Instead, this less common type of breast cancer typically presents as swelling or redness of the breast and can spread quickly. IBC may first be mistaken for an infection or mastitis because of symptoms such as redness and swelling and the frequent lack of a breast lump – all of which can lead to a delay in diagnosis. Patients diagnosed with IBC are diagnosed with later stages of the disease, in part because IBC presents in a different way and is harder to detect. About 30 percent of patients are initially diagnosed with Stage IV, or metastatic disease, which means their breast cancer has already spread to other parts of their body.

Current knowledge about IBC is limited because clinical trials for new breast cancer therapies often restrict the participation of IBC patients, and for those that do allow enrollment, patients’ outcomes are combined with non-IBC patients’ outcomes.

The three organizations have focused on addressing key needs in this understudied form of breast cancer to advance treatments. Their efforts to identify the path to move the field of IBC research forward confirmed researchers and clinicians have a need for a clearer diagnosis and definition of IBC. The current diagnostic criteria have not made significant progress since the 1950s and the current definition of the disease causes patients and research to suffer, resulting in subjective diagnoses and varying treatments.

As part of the work, more than 30 IBC experts across the country have been collaborating on a formal definition of IBC and presented their approach during the 2019 American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Annual Meeting and San Antonio Breast Cancer Symposium. Their work and definition are expected to be published soon in a major oncology journal.

The three organizations have raised $3.4 million to date, which has supported critical programs and research into better understanding IBC. The ongoing work is part of Komen’s mission to save more lives by understanding and treating less common forms of breast cancer.

"We’ve made great progress in identifying and treating breast cancers over the years, but there is still work to do to fully understand and treat aggressive cancers including IBC and metastatic breast cancer, the most advanced stage of breast cancer," said Paula Schneider, President and CEO of Susan G. Komen. "With aggressive breast cancers, patients need more treatment options and they need them quickly. This ongoing partnership is helping us get closer to finding more effective treatments for types of breast cancer that are difficult to treat."

"Since our start over two decades ago, ‘patient-centered’ research has been the buzz word. Our ground-breaking partnership has redefined and initiated true ‘patient-driven’ research to address diagnosis and treatment of Inflammatory Breast Cancer," said Ginny Mason, Executive Director of the IBC Research Foundation. "It’s past time to do more about a disease that continues to steal so many lives."

"It takes true leadership to see beyond the status quo and take bold action to resolve a decades-long issue in IBC diagnosis," said Bryon Davis, CEO of the Milburn Foundation. "This work is pioneering a ‘power to the patient’ movement that connects the dots between worthwhile existing research and a roadmap to successfully coordinated future initiatives."

Nordic Nanovector ASA: Invitation to Q3 2020 Results Presentation and Webcast

On November 16, 2020 Nordic Nanovector ASA (OSE: NANO)reported that it will report its results for the third quarter 2020 on Thursday, 19 November 2020 (Press release, Nordic Nanovector, NOV 16, 2020, View Source [SID1234571185]).

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A presentation by Nordic Nanovector’s senior management team will be webcast live the same day at 8:30am CET.

The webcast can be accessed from www.nordicnanovector.com in the section: Investors & Media and a recording will also be available on this page after the event.

The results report and the presentation will be available at www.nordicnanovector.com in the section: Investors & Media/Reports and Presentation/Interim Reports/2020 from 7:00am CET the same day.

UniSA researchers awarded $2.8 million for new projects

On November 16, 2020 University of South Austral has reported that eight UniSA researchers have collectively secured $2.8 million for six ARC Discovery projects and two Linkage projects (Press release, University of South Australia, NOV 16, 2020, View Source [SID1234571062]).

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ARC Discovery grants have been awarded to the following researchers:

Professor Natasha Harvey (Centre for Cancer Biology) will lead a $613,035 project defining how molecular switches program cell identity during development. This project expects to generate new knowledge in the area of genetics and developmental biology using cutting-edge technologies. The data generated will underpin new approaches to stem cell development to help transplantation;
Professor Sharad Kumar (Centre for Cancer Biology) will lead a $502,000 project focused on the mechanisms that regulate cell death during animal development. The project will combine genetics with proteomics, bioinformatics and cell biology. In the long term the research findings are expected to boost agriculture, food production and human health outcomes;
Associate Professor Anna Sullivan (Education) will lead a $324,000 project to investigate how and why Australian schools use exclusionary practices to manage disorderly students. New policy recommendations are expected to emerge from the project to reduce youth alienation and improve the health and wellbeing of young people;
Professor Nicole Moulding (Justice and Society) will lead a $309,807 project looking at the long-term impacts of childhood emotional abuse, including adverse health outcomes, marginalisation and family violence;
Associate Professor Sue Nichols (Education) will lead a $251,176 project to identify forms of digital exclusion and inclusion on children’s education, investigate a new model of school-home relationships in the digital age, and provide a comprehensive map of digital tools and services.
Dr Bronwyn Hajek (STEM) will lead a $225,000 project to develop a new mathematical model to predict the pattern formation of a new class of permanent lubricant – ionic liquids. The new model is expected to provide a cheap, fast and reliable alternative for screening suitable liquid/surface pairs.
ARC Linkage grants have been awarded to the following researchers:

Associate Professor Drew Evans (Future Industries Institute) will lead a $420,000 project to improve agricultural efficiency, productivity and yield by advancing the understanding of polymer materials interacting with fertiliser. This project is expected to provide a pathway to a world-first real time in-ground fertiliser sensor.
Professor Jun Ma (STEM) will lead a $215,000 project to develop new elastomer/graphene composites which can transform into graphene sheets during melt compounding with elastomers. The outcomes are anticipated to transform the current manufacturing practice of rubber products for applications in agriculture, automobile, construction, medical and mining industries.

Myriad Genetics Announces Global Expansion of Myriad myChoice® Tumor Testing in Europe and China

On November 16, 2020 Myriad Genetics, Inc. (NASDAQ: MYGN), a global leader in molecular diagnostics and precision medicine,reported the expansion of Myriad myChoice tumor testing in several European markets and China (Press release, Myriad Genetics, NOV 16, 2020, View Source [SID1234571110]).

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Myriad myChoice CDx is the industry’s most clinically-validated genomic instability test. The test enables physicians to identify patients with tumors that have lost the ability to repair double-stranded DNA breaks, resulting in potentially increased susceptibility to DNA-damaging drugs such as platinum drugs or PARP inhibitors, including Lynparza (olaparib). A biomarker subgroup analysis of the PAOLA-1 Phase III trial (Olaparib plus Bevacizumab as First-Line Maintenance in Ovarian Cancer, 2019) of Lynparza included patients with advanced ovarian cancer and homologous recombination deficient (HRD)-positive tumors as detected by the myChoice test, including those with BRCA gene mutations. The trial showed that Lynparza in combination with bevacizumab maintenance treatment improved progression-free survival to a median of 37.2 months versus 17.7 months for bevacizumab alone in patients with HRD-positive advanced ovarian cancer. Recently, the European Commission authorized use of Lynparza for the first-line maintenance treatment with bevacizumab of patients with HRD-positive advanced ovarian cancer. Lynparza is jointly developed and commercialized by AstraZeneca (LSE/STO/Nasdaq: AZN) and Merck.

As part of the expansion in Europe, Myriad will license and provide technological support to leading pathology institutes in Germany and France. Additionally, Myriad will support European customers by performing testing out of its clinical laboratory at the company’s global headquarters in Salt Lake City. Also, the institutes in Europe will perform the tests with Myriad’s myChoice CDx PLUS assay. Myriad myChoice CDx PLUS is CE-marked in accordance with the In-Vitro Diagnostic Devices Directive (98/79/EC).

Another collaboration in China provides that Myriad will partner with Burning Rock Biotech, a leader in next generation sequencing technology for precision oncology, to provide myChoice for HRD testing in Phase III clinical studies and clinics throughout China. Myriad will provide Burning Rock with access to its proprietary myChoice technology. The partnership with Burning Rock expands global access to myChoice and positions the test as a preferred developmental companion diagnostic in this important drug development category.

"These new strategic partnerships with leading companies dedicated to advancing the power of precision medicine, reinforce Myriad’s commitment to expanding access to genetic insights for more patients than ever before," said Nicole Lambert, president of Myriad Genetic Laboratories. "Through close collaboration with innovative laboratories in Europe and with Burning Rock in China, we are bringing the clinical benefits of myChoice testing to additional markets and patients, advancing personalized treatment for patients around the world."

In August 2020, myChoice was exclusively cited and the only named commercial companion diagnostic by the American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) in new recommendations on the use of PARP inhibitors for the treatment and management of certain patients with advanced ovarian cancer. The new recommendations, based on clinical trial results, were published in the Journal of Clinical Oncology.

About Myriad myChoice
Myriad myChoice is the most comprehensive homologous recombination deficiency (HRD) test, enabling physicians to identify patients with tumors that have lost the ability to repair double-stranded DNA breaks, resulting in increased susceptibility to DNA-damaging drugs such as platinum drugs or PARP inhibitors. The myChoice test comprises tumor sequencing of the BRCA1 and BRCA2 genes and a composite of three proprietary technologies (loss of heterozygosity, telomeric allelic imbalance and large-scale state transitions). For more information, visit: View Source