AmorChem invests in a new approach to target cancers in which the c-Myc oncogene is deregulated

On February 12, 2020 AmorChem II is reported the funding of a new university project centered on c-Myc, a proto-oncogene involved in more than 50% of human cancers (Press release, Amorchem, FEB 12, 2020, View Source [SID1234554236]). The venture capital fund has signed an agreement with Univalor, the Montreal Clinical Research Institute ("IRCM") and McGill University to support the innovative work of the teams of Dr. Tarik Möröy and Dr. Nicolas Moitessier .

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According to the World Health Organization, cancer is the second largest cause of death in the world. The dysregulation of the oncoprotein c-Myc is a characteristic found in many cancers, notably medulloblastoma, colon cancer and leukemias. However, c-Myc is difficult to target because it does not contain a domain that can easily be reached by a therapeutic molecule. To date, none of the strategies attempted to modulate this target has been clinically successful.

"We were attracted by the innovative approach proposed by the team, namely targeting Miz-1, a c-Myc cofactor essential for its ability to regulate cell cycle progression and apoptosis. This approach seemed very intriguing to us and offers the potential to add a small molecule strategy in immunotherapy, thanks to the increasingly understood role of c-Myc in the biology of T lymphocytes ", says Kevin McBride, partner and chief scientist at AmorChem.

"The participation in KNOCK OUT TM 2019 by Dr. Tarik Möröy and Dr. Nicolas Moitessier convinced us that their respective expertise in molecular biology as well as in medicinal and computational chemistry offer the ideal combination of know-how to overcome the difficulties presented by this target, "explains Inès Holzbaur, managing partner at AmorChem.

"Beyond c-Myc, the platform developed within the framework of the project offers AmorChem the unique opportunity to develop other drugs based on POZ domains by targeting other important targets", adds Elizabeth Douville, managing partner at AmorChem.

"The participation of McGill University in this kind of research with high commercial potential is a major issue for our University," said Sylvain Coulombe, Assistant Vice-Principal, Innovation and Partnerships, McGill University. "Our priority will always be to enable our world-class research to produce innovations that can save lives. This collaboration allows us to be more ready to achieve this goal. "

"The IRCM values ​​collaboration and we are convinced of the benefits of bringing together the best experts around a project. We are therefore delighted to receive the support of AmorChem for this promising collaborative project which aims to develop new therapeutic strategies for the future, "said Max Fehlmann, President and Scientific Director of the IRCM.

"The promotion of university research is not an easy exercise. It requires the involvement of several partners who must work around a common vision of maturation and thus take concerted actions to de-risk innovations and create commercial value. The collaboration between the IRCM, McGill University, Univalor and AmorChem is a very good example of such a partnership. Funding from AmorChem will thus enable the potential of the new platform developed by the teams of Professors Möröy and Moitessier to be validated and its commercial value to be demonstrated, "says Luc Paquet, President and CEO of Univalor.

Moderna to Report Fourth Quarter and Full Year 2019 Financial Results on Wednesday, February 26th, 2020

On February 12, 2020 Moderna, Inc., (Nasdaq: MRNA) a clinical stage biotechnology company pioneering messenger RNA (mRNA) therapeutics and vaccines to create a new generation of transformative medicines for patients, reported that it will host a live conference call and webcast at 8:00 a.m. ET on Wednesday, February 26, 2020 to report its fourth quarter and full year 2019 financial results, and provide a corporate update (Press release, Moderna Therapeutics, FEB 12, 2020, View Source [SID1234554235]).

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To access the live conference call, please dial 866-922-5184 (domestic) or 409-937-8950 (international) and refer to conference ID 3639288. A webcast of the call will also be available under "Events and Presentations" in the Investors section of the Moderna website at View Source The archived webcast will be available on Moderna’s website approximately two hours after the conference call and will be available for 30 days following the call.

AVEO Oncology Announces Publication of Phase 1b/2 Study of Tivozanib in Advanced, Inoperable Liver Cancer in the British Journal of Cancer

On February 12, 2020 AVEO Oncology (NASDAQ: AVEO) reported the publication of results from a monotherapy trial of tivozanib, the Company’s vascular endothelial growth factor receptor tyrosine kinase inhibitor (VEGFR-TKI), in patients with advanced, inoperable hepatocellular carcinoma (HCC) in the British Journal of Cancer (Press release, AVEO, FEB 12, 2020, View Source [SID1234554234]). The article, titled "A multicentre phase 1b/2 study of tivozanib in patients with advanced inoperable hepatocellular carcinoma," is available online first via this link.

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For the Phase 1b/2 tivozanib study, a total of 27 patients were enrolled. The study sought to evaluate the safety, dosing, pharmacokinetics, pharmacodynamics, and preliminary anti-tumor activity of tivozanib in patients with advanced HCC. The recommended Phase 2 dose (RP2D) was determined to be 1.0 mg once daily for 21 days followed by 7 days off treatment on a 28-day cycle. Median progression free and overall survival were 24 weeks and 9 months, respectively, for patients treated at the RP2D, with an overall response rate of 21%. A significant decrease in soluble plasma VEGFR-2 was also observed, suggesting adequate target engagement.

"HCC represents the fastest rising cause of cancer-related death in the U.S., with five-year survival at approximately 26%," said Michael Bailey, president and chief executive officer. "This study is an important steppingstone in understanding tivozanib’s safety and efficacy in HCC, and was the foundation for our ongoing Phase 1b/2 DEDUCTIVE study of tivozanib in combination with IMFINZI (durvalumab). As we work toward our expected filing of a New Drug Application with the FDA this quarter for tivozanib in kidney cancer, we look forward to expanding our tivozanib-immunotherapy clinical strategy as part of our effort to maximize its long-term potential."

Enrollment is currently underway in a Phase 1b/2 DEDUCTIVE study of tivozanib in combination with IMFINZI (durvalumab), AstraZeneca’s human monoclonal antibody directed against programmed death-ligand 1 (PD-L1), in patients with HCC who have not received prior systemic therapy. The trial is being conducted as part of a clinical collaboration between AVEO and AstraZeneca.

"In a number of solid tumor indications, including metastatic liver cancer, VEGF-TKI/immunotherapy combinations are playing an increasingly important role in initial treatment selection," said Renuka Iyer, M.D., senior author of the publication and Professor of Oncology and Co-Director, Liver and Pancreas Tumor Center, Roswell Park Comprehensive Cancer Center. "Central to these combinations is the tolerability of the VEGF-TKI backbone. With an early efficacy signal and favorable tolerability profile demonstrated in this study, tivozanib shows great potential as a VEGF-TKI for such combinations. I look forward to seeing this potential elucidated in the ongoing DEDUCTIVE study of tivozanib and durvalumab in HCC."

About Tivozanib

Tivozanib (FOTIVDA) is an oral, once-daily, vascular endothelial growth factor receptor (VEGFR) tyrosine kinase inhibitor (TKI) discovered by Kyowa Kirin and approved for the treatment of adult patients with advanced renal cell carcinoma (RCC) in the European Union plus Norway, New Zealand and Iceland. It is a potent, selective and long half-life inhibitor of all three VEGF receptors and is designed to optimize VEGF blockade while minimizing off-target toxicities, potentially resulting in improved efficacy and minimal dose modifications.1,2 Tivozanib is being studied in the TIVO-3 trial, which is intended to support a regulatory submission of tivozanib in the U.S. as a treatment for relapsed/refractory RCC. Tivozanib has been shown to significantly reduce regulatory T-cell production in preclinical models3 and has demonstrated synergy in combination with nivolumab (anti PD-1) in a Phase 2 study in RCC4. Tivozanib has been investigated in several tumor types, including renal cell, hepatocellular, colorectal, ovarian and breast cancers.

Illumina to Webcast Upcoming Investor Conference Presentations

On February 12, 2020 Illumina, Inc. (NASDAQ:ILMN) reported that its executives will be speaking at the following investor conferences and invited investors to participate via webcast (Press release, Illumina, FEB 12, 2020, View Source [SID1234554233]).

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SVB Leerink Global Healthcare Conference in New York, NY
Wednesday, February 26, 2020 at 11:00 a.m. Eastern Time

Cowen Annual Health Care Conference in Boston, MA
Tuesday, March 3, 2020 at 11:20 a.m. Eastern Time

The live webcasts can be accessed in the Investor Relations section of Illumina’s web site under the "company" tab at www.illumina.com. A replay of the presentations will be posted on Illumina’s website after the event and will be available for at least 30 days following.

Arcus Biosciences to Present at the 9th Annual SVB Leerink Global Healthcare Conference

On February 12, 2020 Arcus Biosciences, Inc. (NYSE:RCUS), an oncology-focused biopharmaceutical company working to create best-in-class cancer therapies, reported that management will present at the 9th Annual SVB Leerink Global Healthcare Conference on Wednesday, February 26, 2020 at 9:30 a.m. Eastern Time in New York, NY (Press release, Arcus Biosciences, FEB 12, 2020, View Source [SID1234554232]).

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A live audio webcast of the presentation will be available by visiting the "Investors" section of the Arcus website at www.arcusbio.com. A replay of the webcast will be available for at least 30 days following the live event.