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

On January 6, 2020 Jazz Pharmaceuticals plc (Nasdaq: JAZZ) reported that the company will be webcasting its corporate presentation at the 38th Annual J.P. Morgan Healthcare Conference in San Francisco, CA (Press release, Jazz Pharmaceuticals, JAN 6, 2020, View Source [SID1234552751]).

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Bruce Cozadd, chairman and chief executive officer, will provide an overview of the company and a business and financial update at the conference on Monday, January 13, 2020 at 10:00 a.m. PST / 6:00 p.m. GMT.

A live audio webcast of the presentation may be accessed from the Investors section of the Jazz Pharmaceuticals website at www.jazzpharmaceuticals.com. Please connect to the website prior to the start of the presentation to ensure adequate time for any software downloads that may be necessary to listen to the webcast.

An archive of the webcast will be available on the website for at least one week following the presentation on the Investors section of the company’s website at www.jazzpharmaceuticals.com.

Centene To Present At 38th Annual J.P. Morgan Healthcare Conference

On January 6, 2020 Centene Corporation (NYSE: CNC) reported it will present at the 38th Annual J.P. Morgan Healthcare Conference, to be held at the Westin St. Francis Hotel in San Francisco, January 13-16, 2020 (Press release, Centene , JAN 6, 2020, View Source [SID1234552750]).

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Centene will present on Monday, January 13th, at 7:30 a.m. Pacific Standard Time (PST). A simultaneous live audio webcast is available at: View Source

A webcast replay of this presentation will be available afterwards via the Company’s website at www.centene.com under the Investors section.

InxMed Announces Clinical Collaboration with MSD to Evaluate IN10018 in Combination with Pembrolizumab

On January 6, 2019 InxMed (Shanghai) Co., Ltd., a clinical stage biotech company dedicated to developing innovative, individualized medicines with international impact, reported that the company has entered into a clinical collaboration with a subsidiary of Merck & Co, Inc. Kenilworth, NJ U.S.A., known as MSD outside the United States and Canada, to evaluate IN10018, an investigational proprietary focal adhesion kinase (FAK) inhibitor in combination with pembrolizumab, MSD’s anti-PD-1 therapy, in patients with pancreatic cancer (Press release, InxMed, JAN 6, 2020, View Source [SID1234552749]). InxMed will be the study sponsor and MSD will provide pembrolizumab to InxMed to use in the clinical study. This is the first global clinical collaboration between the two companies.

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Dr. Zaiqi Wang, InxMed’s Chairman and CEO, commented: "IN10018 is an innovative best-in-class FAK inhibitor with significant effect on tumor micro-environment, a critical component to conquer tumor. We are very excited that MSD has collaborated with InxMed with the goal of developing additional treatment options for patients with pancreatic cancer through the evaluation of IN10018 in combination with pembrolizumab. This collaboration marks an important step forward for InxMed to steadily implement its best in disease combination strategy. We look forward to working with MSD to find a better solution for this deadly disease."

Dr. Manuel Hidalgo Medina, M.D., Ph.D., Chief of the Division of Hematology and Medical Oncology and Senior Member of the Sandra and Edward Meyer Cancer Center at Weill Cornell Medicine and New York Presbyterian/Weill Cornell Medical Center and a world leading expert in pancreatic cancer, said: "There is a huge unmet medical need for pancreatic cancer patients and we need to tackle both cancer cells and tumor stroma to make future therapeutics work. FAK inhibitors could enhance pancreatic cancer treatment in combination with other therapeutic modalities."

"Stroma is a significant issue for pancreatic cancer patients. Our recent research has indicated that, mechanistically, FAK inhibitors could significantly reduce the level of stroma and fibrosis and therefore enable the penetration of therapeutic agents to render/sensitize pancreatic cancers to either chemotherapy or immunotherapy," said Dr. Paul Timpson, Professor at the Garvan Institute of Medical Research in Sydney, a leading expert in the studies of tumor stroma and therapeutic resistance, and author in Science and Translational Research and Nature Communication.

About IN10018

IN10018, formerly known as BI853520, is a potent and selective ATP-competitive focal adhesion kinase (FAK) small molecule inhibitor under clinical development stage in both the United States and China. InxMed owns the exclusive global rights for development and commercialization. Early clinical data of IN10018 has demonstrated a favorable safety profile and promising efficacy signals against a number of tumor types. With solid underlying disease biology, IN10018 has also shown potency to overcome fibrotic barrier and immune tolerance, boost multi-modalities including targeted therapy, chemotherapy, immune-therapy, and have potential to be an anchor molecule for further exploration of combination therapy.

Silicon Therapeutics Expands Leadership Team with Key Appointments in Clinical Development and Strategy as well as Computational Physics

On January 6, 2020 Silicon Therapeutics reported three additions to its management team to help lead the company through its next stage of growth. Humphrey Gardner, MD, FCAP has joined the company as Chief Medical Officer; Christopher Borella, PhD, has joined as Vice President, Head of Operations; and Huafeng Xu, PhD, has joined as Chief Technology Officer (Press release, Silicon Therapeutics, JAN 6, 2020, View Source [SID1234552747]).

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"The appointments of Humphrey and Chris, who bring deep expertise in clinical development and strategy, reflect the progress we have made in building and advancing our oncology pipeline," said Lanny Sun, Silicon Therapeutics Co-founder and CEO. "They will play key roles as our lead STING agonist enters clinical trials and our other programs advance towards the clinic. Huafeng will strengthen our leadership in computational physics, bringing over 15 years of experience in methods and theory development."

Dr. Gardner joins Silicon from Evelo Biosciences, where he served as Chief of Medical Oncology and led oncology discovery as well as the IND and clinical development of their first microbial cancer immune therapy. Previously, he served as Vice President of Early Clinical Development in both Infection and in Oncology at AstraZeneca, and as Senior Vice President of Clinical Development at Karyopharm. Prior to these appointments, he led the Oncology Translational Laboratories at Novartis, and various discovery and translational programs at Biogen. Before joining industry, Dr. Gardner was an Assistant Professor of Cell Biology at The Scripps Research Institute. Dr. Gardner obtained his BA in Biochemistry and his MB, BChir, at the University of Cambridge, UK. He did his specialty training in anatomic pathology at the Beth Israel Hospital, Harvard Medical School. He completed his postdoctoral fellowship at the Whitehead Institute in the laboratory of Professor Rudolf Jaenisch. Dr. Gardner has over 100 publications and patents in fields including oncology, neuroscience, rheumatology, and diagnostics.

Dr. Borella joins Silicon Therapeutics from Agios Pharmaceuticals where he was the Head of Early Stage Program Management and Project Leader for their MAT2A franchise. During his 8+ years at Agios, Chris and his team were directly involved in bringing seven drug candidates including two marketed drugs, Tibsovo (ivosidenib) and Idhifa, (enasidenib) forward into the clinic. Prior to Agios Therapeutics, Dr. Borella held project leadership positions at both Proteostasis and Synta Pharmaceuticals. He received his PhD in Medicinal Chemistry from Stony Brook University and was a post-doctoral fellow at Memorial Sloan Kettering Cancer Center.

Dr. Xu joins Silicon Therapeutics after 12 years at D. E. Shaw Research, the leading institution in method and hardware development for molecular simulations, where he played an early role in designing the specialized Anton chip for molecular dynamics simulations, and he led the development of the methods and software for free energy calculations that are now widely used in the pharmaceutical industry. He has also pioneered the application of long-timescale molecular simulations and statistical mechanical theory in revealing fundamental mechanisms of molecular recognition in immunology and virology. Dr. Xu started his career in the biotechnology industry at 3-Dimensional Pharmaceuticals. He earned his Bachelor of Science from Peking University and his M.S. and Ph.D. degrees from Columbia University. He was a visiting postdoctoral scholar in University of California, San Francisco.

Guided Therapeutics Raises Funds Aimed at Increasing International Sales and Restarting US FDA Approval Process

On January 6, 2020 Guided Therapeutics, Inc. (Pink Sheets: GTHP), the maker of a rapid and painless cervical cancer detection test based on its patented biophotonic technology, reported the closing of two separate investments: The first, a Convertible Note issued to Auctus Fund, LLC for $2.4 Million, occurs in three tranches (Press release, Guided Therapeutics, JAN 6, 2020, View Source [SID1234552746]). The first tranche of $700,000 has been received, while the second tranche of $400,000 is contingent upon filing an S-1 registration statement while the last tranche of $1,300,000 is due within 60 days of the S-1 becoming active. Conversion prices of the tranches are based on market price and have a floor of 15 cents per share. Auctus also will receive three year warrants, a portion exercisable at twenty cents and a portion at twenty-five cents. A second financing of $742,000 also closed and is a unit offering consisting of two common shares and preferred shares convertible into three common shares per dollar invested, with four warrants, half exercisable at twenty-five cents and half at seventy-five cents per share. Investors include Company Board Members and other qualified institutional and individual investors.

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As a condition of these investments, the Company also needed to achieve significant debt reduction and capitalization restructuring which eliminated variable price convertible debt without floor pricing similar to the new investments. To these ends, the Company has executed agreements to pay off a significant portion of its debt and exchange variable pricing instruments for a combination of cash, common shares and warrants at fixed exercise pricing. The net effect of these transactions, after the last tranche of the Auctus investment is received, is a reduction of debt by over $7 million. Over the past year, including the transactions reported in this announcement, the Company’s debt has been reduced by over $10 million.

"The nearly $3.2 million in near term financing will allow the company to expand international sales and restart its FDA approval process, while at the same time significantly reduces debt and exposure to excessive dilution", said CEO Gene Cartwright. "The net effect has been to place the company on much firmer footing as it eyes new regulatory approvals and sales orders from China, Russia, the Middle East and the EU in 2020."