On July 11, 2019 Physicians’ Education Resource, LLC (PER), a worldwide leading resource for continuing medical education, reported that it has released the agenda for the 37th Annual Chemotherapy Foundation Symposium: Innovative Cancer Therapy for Tomorrow (Press release, Physicians’ Education Resource, JUL 11, 2019, View Source [SID1234537487]). The conference will take place Nov. 6-8 at the New York Marriott Marquis in New York City.

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"This fall we look forward to having oncology professionals from around the world attend our three-day marquee oncology CME conference in New York City," said Phil Talamo, president of PER. "Oncology data is evolving at an unprecedented rate, and the opportunities to share clinical experience across tumors, particularly with novel targeted agents and immunotherapies, are needed for the cancer team to provide state-of-the-art treatments. This year’s meeting will focus on the cutting edge of medicine, and how new treatments are trailblazing contemporary oncology care."

Each year, the Chemotherapy Foundation Symposium: Innovative Cancer Therapy for Tomorrow brings together more than 1,000 health care professionals for three days to network with the top minds in oncology. At this year’s meeting, activity co-chairs — Drs. Adam M. Brufsky, Benjamin P. Levy and William K. Oh — will be joined by 100 internationally world-renowned experts who will provide attendees with expert insights on the latest developments in cancer therapeutics, offering an unparalleled opportunity to learn how innovative approaches fit into existing treatment paradigms to optimize care and outcomes for their patients with cancer.

Additionally, the PER Educator of the Year award, which highlights the accomplishments of oncology leaders and honors their contributions and efforts to propel the field of medical oncology through innovative and collaborative education will also be presented at this year’s conference.

For more information and to view the agenda or register, click here.

On July 11, 2019 Sengenics, the functional proteomics company, reported that it has joined the Foundation for the National Institutes of Health (FNIH) Biomarkers Consortium (Press release, Sengenics, JUL 11, 2019, View Source [SID1234537486]). As a member of the consortium, Sengenics aims to further accelerate the identification and commercialisation of autoantibody biomarkers for early diagnosis of cancer and autoimmune diseases as well as development of new companion diagnostics tests.

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The FNIH Biomarkers Consortium was co-founded by the U.S. National Institutes of Health (NIH), the U.S. Food and Drug Administration (FDA), the Pharmaceutical Research and Manufacturers of America (PhRMA), the Centers for Medicare & Medicaid Services (CMS) and BIO. It counts amongst its list of contributing members, major pharmaceutical companies such as Novartis, GSK and Merck; as well as not-for-profit organisations such as the Alzheimer’s Drug Discovery Foundation and the American Heart Association.

Sengenics will work with the FNIH Biomarkers Consortium to provide expertise about the discovery of autoantibodies for diagnostics, companion diagnostics and therapeutics applications, particularly through its proprietary KREX technology. As KREX-based protein arrays use antigens that are correctly folded and functional, autoantibodies are detected with very high specificity and sensitivity. The technology has already been applied to discover autoantibody biomarkers with both diagnostic and protective potential for cancers, autoimmune diseases and neurodegenerative disorders. KREX protein arrays have also been used for stratification of patients into responders, non-responders and those exhibiting immune-related adverse events (irAEs). This has been achieved with very high positive predictive values (PPV) and negative predictive values (NPV) for patients on autoimmune or immune checkpoint inhibitor drugs.

Joseph P. Menetski, Ph.D., Associate Vice President for Research Partnerships, FNIH said, "Autoantibodies are fundamental biomarkers for cancer and autoimmune disease diagnostics. We believe that Sengenics’ expertise will be complementary to the FNIH Biomarker Consortium’s key focus areas in terms of the rapid identification, development and qualification of potential high-impact biomarkers for improvements in drug development, clinical care and regulatory decision-making. We are looking forward to Sengenics making a positive contribution in terms of advancing medical diagnostics and research within the consortium."

Speaking on the collaboration, Chief Scientific Officer of Sengenics, Jonathan Blackburn, D.Phil., said, "We are delighted to join the FNIH Biomarkers Consortium. We see this as an important vehicle to collaborate with industry experts and partners across the biomarker discovery and commercialisation chain. In the last year, we have seen our technology becoming established as the benchmark for high specificity and sensitivity autoantibody detection by both the pharmaceutical industry as well as leading academic institutions. Our fundamental aim going forward is to apply our technology to patient-centric, autoantibody-based, translational diagnostics tests for both precision medicine and early disease detection applications."

On July 11, 2019 The Ivy Brain Tumor Center at the Barrow Neurological Institute has reported a partnership with Karyopharm Therapeutics (Nasdaq:KPTI) to accelerate the treatment of brain cancer (Press release, The Ivy Brain Tumor Center, JUL 11, 2019, View Source [SID1234537485]). The Ivy Brain Tumor Center will employ Karyopharm’s first-in-class oral Selective Inhibitor of Nuclear Export (SINE) compound, selinexor, in combination with other new-in-class drugs, as a dual-drug experimental therapy for adult glioblastoma.

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"We are highly motivated to study novel drug combination strategies with selinexor to potentially advance the available treatment options for patients with glioblastoma, one of the most aggressive forms of brain cancer"

This academic-private partnership will begin with a preclinical study targeting the protein XP01 in glioblastoma patients and testing several new drug cocktails involving selinexor. Based on detailed pharmacodynamic and pharmacokinetic analyses, the lead drug cocktail will then be pursued as a combined-drug trial within the Ivy Brain Tumor Center’s Phase 0 clinical trial portfolio. This unique trial format will enable researchers to understand if the experimental therapy is impacting an individual patient’s brain tumor in as little as seven days, therefore saving valuable patient time.

Drug development for glioblastoma has remained stagnant for decades, with the latest FDA-approved therapy associated with a survival benefit occurring in 1999. The Ivy Brain Tumor Center, a nonprofit clinical trials program funded by the largest grant in the history of brain tumor research, is challenging the status quo of conventional drug development by streamlining early-phase identification of promising agents through tissue-based Phase 0 trialing.

"Selinexor exploits a compelling target in glioblastoma patients, which is why we have selected it as the backbone of a new experimental drug cocktail," said Dr. Nader Sanai, director of the Ivy Brain Tumor Center. "Our scientific partnership with Karyopharm Therapeutics will arrive at a new therapeutic strategy that can be accelerated into the clinic and patients in need."

Developed by Karyopharm Therapeutics, selinexor is the first in a new family of investigational therapies known as Selective Inhibitor of Nuclear Export (SINE) compounds and is currently being evaluated in Phase 2 and 3 clinical trials for multiple myeloma, diffuse large B-cell lymphoma (DLBCL), and a variety of solid tumors. It functions by blocking the nuclear export protein XPO1, forcing accumulation and activation of tumor suppressor proteins.

"We are highly motivated to study novel drug combination strategies with selinexor to potentially advance the available treatment options for patients with glioblastoma, one of the most aggressive forms of brain cancer," said Sharon Shacham, PhD, MBA, president and chief scientific officer of Karyopharm. "We share the Ivy Brain Tumor Center’s sense of urgency and commitment to pursuing future breakthroughs in glioblastoma treatment and look forward to our partnership in this important and innovative research endeavor."

On July 11, 2019 Schrödinger reported receipt of a preclinical milestone payment from Sanofi in a drug discovery program advancing as part of a multi-year, multi-target collaboration between the two companies (Press release, Schrodinger, JUL 11, 2019, View Source [SID1234537484]).

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Under the terms of the collaboration, Schrödinger provides advanced molecular simulation and computational design expertise to Sanofi across multiple stages of drug discovery, from target analysis and lead optimization to identification of a development candidate. Earlier this spring, Schrödinger announced the advancement of a separate program in autoimmune disease into clinical trials.

"This is an especially exciting moment in our collaboration with Sanofi as it marks another program advanced," said Karen Akinsanya, Ph.D., Schrödinger’s chief biomedical scientist. "Achieving this milestone is a testament to the value of our ongoing collaboration with partners and our ability to efficiently identify promising therapeutic compounds."

The work with Sanofi is one of several collaborations Schrödinger has established with leading biotech and pharmaceutical companies around the world. These collaborations leverage Schrödinger’s physics-based computational platform to enable rapid iterations of design and analysis of potential therapeutic compounds. Such collaborations have already led to several clinical-stage assets and two FDA-approved oncology drugs. More than two dozen additional programs are moving through discovery and development in indications including oncology, diabetes, metabolic disorders, schizophrenia, and neurodegenerative diseases.

On July 11, 2019 SOTIO and Cytune Pharma, members of the PPF Group, reported the first dosing of cancer patients with SO-C101, a superagonist fusion protein of interleukin IL-15 (Press release, SOTIO, JUL 11, 2019, View Source [SID1234537483]). The phase I/Ib study (SC103) will evaluate the safety and preliminary efficacy of SO-C101 in patients with selected advanced/metastatic solid tumors.

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The first patient was treated with SO-C101 at the Institute Gustave Roussy (France). The SC103 clinical trial will also enrol patients in the Vall d’Hebron cancer center (Spain) and, subject to obtaining all the necessary approvals, at the Yale Cancer Center in New Haven, CT and MD Anderson Cancer Center in Houston, TX. Cytune Pharma is responsible for the clinical development of SO-C101, SOTIO is sponsor of the SC103 clinical trial.

Aurélien Marabelle, M.D., Ph.D., coordinating investigator of the phase I/Ib trial said: "I am very pleased that our medical center has enrolled the first patient in this important clinical trial. We believe that SO-C101 has the potential to make a life-changing difference to many patients with difficult-to-treat forms of cancer. I am looking forward to further advancing this innovative therapy."

"SO-C101 is a very innovative approach which has been validated for its efficacy and safety in preclinical experiments. Since SO-C101 is an ideal combination partner for checkpoint inhibitors, monoclonal antibodies and other well established therapies, the planning for additional combination trials is already ongoing," said Radek Spisek, M.D., Ph.D., CEO of SOTIO.

"I’m excited that after 12 years of research and development at Cytune Pharma, which was based on previous research from INSERM and the University of Nantes and supported by Bpifrance and Atlanpole Biotherapies, our invention has now entered the clinical development phase. I hope that SO-C101 will become a treatment for cancer patients in the future," adds David Bechard, Ph.D., President and COO of Cytune Pharma.

Description of clinical trial
SC103 (Eudra CT: 2012-002814-38): A multicenter open-label phase 1/1b study to evaluate the safety and preliminary efficacy of SO-C101 as monotherapy and in combination with pembrolizumab in selected patients with advanced/metastatic solid tumors. SOTIO received a positive decision allowing launch of SC103 clinical trial within the EU Voluntary Harmonisation Procedure (VHP) in February 2019.