Blueprint Medicines to Host Conference Call to Review Updated Clinical Data for Pralsetinib in RET-Altered Cancers on Friday, May 29, 2020

On May 26, 2020 Blueprint Medicines Corporation (NASDAQ:BPMC), a precision therapy company focused on genomically defined cancers, rare diseases and cancer immunotherapy, reported that it will host a live conference call and webcast at 8:30 a.m. ET on Friday, May 29, 2020 to review updated clinical data for pralsetinib in RET-altered cancers (Press release, Blueprint Medicines, MAY 26, 2020, http://ir.blueprintmedicines.com/news-releases/news-release-details/blueprint-medicines-host-conference-call-review-updated-clinical [SID1234558476]). The data will also be presented in the American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) 2020 (ASCO20) Virtual Scientific Program, May 29-31, 2020.

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Conference Call Information

To access the live call, please dial (855) 728-4793 (domestic) or (503) 343-6666 (international) and refer to conference ID 8585078. A webcast of the conference call will be available in the Investors & Media section of Blueprint Medicines’ website at View Source The archived webcast will be available on Blueprint Medicines’ website approximately two hours after the conference call and will be available for 30 days following the call.

Xencor to Present at Upcoming Investor Conferences

On May 26, 2020 Xencor, Inc. (NASDAQ: XNCR), a clinical-stage biopharmaceutical company developing engineered monoclonal antibodies for the treatment of cancer and autoimmune diseases, reported that Bassil Dahiyat, Ph.D., president and chief executive officer, will participate in two upcoming investor conferences (Press release, Xencor, MAY 26, 2020, View Source [SID1234558494]):

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Jefferies Virtual Healthcare Conference
Date: Tuesday, June 2, 2020
Presentation Time: 2:30 p.m. ET / 11:30 a.m. PT
Raymond James Human Health Innovation Conference
Date: Monday, June 15, 2020
Immuno-Oncology Panel Time: 11:00 a.m. ET / 8:00 a.m. PT
A live webcast of the presentation at the Jefferies conference will be available under "Events & Presentations" in the Investors section of the Company’s website located at www.xencor.com. A replay will be posted on the Xencor website approximately one hour after the live event and will be available for 30 days.

Medivir Appoints Yilmaz Mahshid as New CEO

On May 26, 2020 Medivir AB (Nasdaq Stockholm: MVIR) reported that its Board of Directors has appointed Yilmaz Mahshid as the new CEO of the company (Press release, Medivir, MAY 26, 2020, View Source [SID1234558511]). Yilmaz Mahshid has long and broad experience from qualified roles in the life science sector. He succeeds Uli Hacksell, who has been CEO since October 2018. Yilmaz Mahshid will assume his position in the fall. Uli Hacksell remains as a board member of Medivir.

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Yilmaz Mahshid joins Medivir from his recent position as CFO at PledPharma. He was prior to that Investment Manager at Industrifonden. He has also worked as a health care analyst at Pareto Securities and at Öhman Fondkommission. Yilmaz holds a doctorate from the Department of Medical Biochemistry and Biophysics at Karolinska Institute. He began his career as a researcher at the Karolinska Institute followed by the pharmaceutical companies Biolipox and Orexo.

– Uli Hacksell assumed leadership responsibility for Medivir as acting CEO in the fall of 2018 in conjunction with the strengthened focus on clinical cancer projects and a comprehensive restructuring of the company. Uli has invested enormous energy in shaping and developing Medivir into the company it is today. When we looked for Uli’s successor, important parameters were experience, a strong scientific foundation, knowledge and insight about the industry as well as the investor perspective. In Yilmaz Mahshid we have found what we were looking for and it is my great pleasure to welcome him to Medivir", says Helena Levander, Chairman of Medivir’s Board of Directors.

– Going forward, Uli will still be strongly involved in the company’s development in his role as board member. We are extremely grateful that he led the strategically important transformation of Medivir", continues Helena Levander.

– I believe that Yilmaz will be perfect as new CEO of Medivir. He is extremely qualified and has the background, drive and strategic thinking that our exciting company needs. I will stay on as CEO until Yilmaz takes over. Shortly after the handover I will return to function solely as a board member, but I will of course be available as a sparring partner whenever Yilmaz so wishes.", says Uli Hacksell, CEO at Medivir.

Medivir AB is obliged to make this information public pursuant to the EU Market Abuse Regulation. The information was submitted for publication, through the agency of the contact person set out above, at 08.30 CET on May 26, 2020.

Using the CRISPR/Cas3 Genome Editing Technology by Noil Immune Biotech and C4U About PRIME allogeneic CAR-T cell therapy partnership

On May 25, 2020 Nail Imune Biotech Co., Ltd. (Location: Minato-ku, Tokyo, hereinafter "Noil Imune") and C4U Co., Ltd. (Location: Suita, Osaka Prefecture, hereinafter "C4U") are now editing the next-generation genome of C4U (Press release, Noile-Immune Biotech, MAY 25, 2020, View Source [SID1234561509]). Combining the CRISPR/Cas3 technology, which is a technology, with the PRIME (Proliferation inducing and migration enhancing) technology for adapting genetically modified immune cell therapies such as CAR-T and TCR-T possessed by Noil Imune to solid cancer We would like to inform you that we have signed an agreement for joint research and commercialization of cross-type allogeneic genetically modified immune cell therapy technology.

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The CRISPR/Cas3 technology, which is the basic technology of C4U, is the research result of Prof. Tomoshi Mashita of the Institute of Medical Science, University of Tokyo, who is the founding member of C4U and advisor of science and technology, and Professor Junji Takeda of the Institute of Microbial Diseases, Osaka University. A new genome editing technology using the CRISPR/Cas3 system developed based on It is a technology that can counter the CRISPR/Cas9 system, which is currently being researched all over the world, and is attracting attention as a promising genome editing technology that is not affected by the complicated patent situation regarding Cas9.

In addition, PRIME technology, which is the basic technology of Noyle Immune, is the scientific founder and director of Noyle Immune, and Professor Koji Tamada of the Graduate School of Medicine, Yamaguchi University (Professor, Gene and Cell Therapy Center, Institute of Medical Science, University of Tokyo). It is a technology related to cancer immune cell therapy such as CAR-T developed by et al. CAR-T is a technology that not only enhances the functions of CAR-T, etc. by producing cytokines and chemokines, but also causes cancer injury by cancer patients’ own endogenous immune cells.

"I am very pleased to be able to form a business alliance with C4U, which has excellent genome editing technology of its own." In this project, we will combine the PRIME CAR-T technology of Noil Imune and the genome editing technology of C4U. By combining these, we will promote the development of highly active CAR-T cells that utilize immune cells derived from alleles.The combination of domestic technologies is highly versatile and can exert therapeutic effects even on solid cancers. We hope that next-generation CAR-T cells will be developed and a treatment method that will save more patients will be created.This project is based on the Ministry of Education, Culture, Sports, Science and Technology subsidy project "Regional Innovation Ecosystem Formation Program". We are aiming to develop the world’s most advanced cancer immunotherapy with the help of various researches including the beginning."

In addition, C4U’s Satoshi Mashita said, "The PRIME CAR-T technology possessed by Noyle Imune is a wonderful technology that can be proud of in the world, which has successfully overcome the effects of CAR-T cells on solid cancer, which was a weak point, and the sustainability of the effects. By adding our newly developed CRISPR/Cas3 genome editing technology to this technology, it is possible to achieve a more inexpensive, more effective and superior allogeneic CAR-T cell therapy compared to the existing CAR-T cell therapy. I am confident that we will be able to provide to many suffering patients."

Neil Imune and C4U will collaborate on allogeneic genetically modified immune cell therapy under this partnership. Neil Imune will bear part of the costs necessary to carry out this joint research. In addition, both companies have the right to commercialize the results obtained by this joint research, and the right to mutually receive royalties based on the contract. Noil Imune will pay the access fee for the basic technology of C4U when commercializing. Further details of the contract are not disclosed.

Imago BioSciences To Present Update on Phase 2 results of Bomedemstat (IMG-7289), a Lysine Specific Demethylase-1 (LSD1) Inhibitor for the Treatment of Myelofibrosis (MF)

On May 25, 2020 Imago BioSciences, Inc. ("Imago"), a clinical stage biopharmaceutical company developing innovative treatments for myeloid diseases, reported that positive Phase 2 data from its lead pipeline program bomedemstat (IMG-7289), will be presented at the Virtual Edition of the 25th EHA (Free EHA Whitepaper) Annual Congress beginning June 12, 2020 (Press release, Imago BioSciences, MAY 25, 2020, View Source [SID1234558429]).

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Title: A PHASE 2 STUDY OF BOMEDEMSTAT (IMG-7289), A LYSINE-SPECIFIC DEMETHYLASE-1 (LSD1) INHIBITOR, FOR THE TREATMENT OF LATER-STAGE MYELOFIBROSIS (MF)

Session Topic: 16. Myeloproliferative Neoplasms

Final Abstract Code: EP1080

The data demonstrates the potential of bomedemstat as a monotherapy in intermediate-2 and high-risk patients with myelofibrosis who have become intolerant of, or resistant to, or are ineligible for a Janus Kinase (JAK) inhibitor.

Imago is currently conducting a Phase 2 study of bomedemstat in five countries. Clinical endpoints include spleen volume reduction, reduction in total symptom scores, and improvement in circulating inflammatory cytokines, anemia, bone marrow fibrosis and blast count. For additional information, visit cliniciatrials.gov (NCT03136185).

About Bomedemstat (IMG-7289)

Bomedemstat is being evaluated in an open-label Phase 2 clinical trial for the treatment of advanced myelofibrosis (MF), a bone marrow cancer that interferes with the production of blood cells. The endpoints include spleen volume reduction and symptom improvement at 12 and 24 weeks of treatment. Bomedemstat is used as monotherapy in patients who are resistant to, intolerant of, or ineligible for a Janus Kinase (JAK) inhibitor.

Bomedemstat is a small molecule developed by Imago BioSciences that inhibits lysine-specific demethylase 1 (LSD1 or KDM1A), an enzyme shown to be vital in cancer stem/progenitor cells, particularly neoplastic bone marrow cells. In non-clinical studies, IMG-7289 demonstrated robust in vivo anti-tumor efficacy across a range of myeloid malignancies as a single agent and in combination with other chemotherapeutic agents. Bomedemstat (IMG-7289) is an investigational agent currently being evaluated in ongoing clinical trials (ClinicalTrials.gov Identifier: NCT03136185 and NCT02842827). Bomedemstat has FDA Orphan Drug and Fast Track Designation for the treatment of myelofibrosis and essential thrombocythemia, and Orphan Drug Designation for treatment of acute myeloid leukemia.