Sengenics, a Leading Precision Medicine Focused Company, to Present at the Annual BIO CEO and Investor Conference

On January 28, 2020 Sengenics, a leading precision medicine focused company, reported that Dr Arif Anwar, CEO of Sengenics, will present a company overview at the 2020 BIO CEO and Investor Conference (Press release, Sengenics, JAN 28, 2020, View Source [SID1234553629]). The presentation will take place at 3:15 PM EST on Monday, February 10, 2020 in the Wilder room at the New York Marriott Marquis.

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Dr Arif Anwar will present an overview of the commercialisation strategy of the company and applications of its patented KREXTM technology for autoimmune and cancer immunotherapy drug response and ADR prediction.

Sengenics is currently co-developing complementary and companion diagnostic tests for several autoimmune and cancer immunotherapy drugs through partnerships with top pharmaceutical companies. The company has commenced the process for obtaining FDA 510(k) approval for several of these tests and plans to launch them in 2020 and 2021.

Sengenics’ management team will also hold meetings with institutional investors and analysts from February 10 – 14 in New York. Accredited investors are invited to request a meeting during the conference through BIO’s One-on-One PartneringTM System.

Cerus Corporation Announces Public Offering of Common Stock

On January 28, 2020 Cerus Corporation (Nasdaq: CERS) reported that it has commenced a registered underwritten public offering of $50.0 million of its common stock (Press release, Cerus, JAN 28, 2020, View Source [SID1234553613]). In addition, Cerus expects to grant the underwriter a 30-day option to purchase up to an additional $7.5 million of its common stock. All of the shares to be sold in the offering are to be sold by Cerus.

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BTIG, LLC is acting as sole book-running manager for the offering.

A shelf registration statement on Form S-3 (File No. 333-219727) relating to the shares of common stock described above was previously filed by Cerus with the Securities and Exchange Commission ("SEC") and declared effective on January 8, 2018. A preliminary prospectus supplement related to the offering will be filed with the SEC. Prospective investors should read the preliminary prospectus supplement, when available, and the accompanying prospectus and other documents Cerus has filed with the SEC for more complete information about Cerus and the proposed offering. These documents are available at no charge by visiting the SEC’s website at View Source Alternatively, copies of the preliminary prospectus supplement, when available, and the accompanying prospectus may be obtained by contacting BTIG, LLC at 65 East 55th Street, New York, NY, 10022, by email at [email protected] or by telephone at (212) 593-7555.

This press release shall not constitute an offer to sell or the solicitation of an offer to buy, nor shall there be any sale of these securities in any state or jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification of these securities under the securities laws of any such state or jurisdiction.

European Medicines Agency Validates Kite’s Marketing Application for Company’s Second CAR T Cell Therapy

On January 28, 2020 Kite, a Gilead Company (Nasdaq: GILD), reported that the company’s Marketing Authorization Application (MAA) for KTE-X19, an investigational chimeric antigen receptor (CAR) T cell therapy for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (MCL), has been fully validated and is now under evaluation by the European Medicines Agency (EMA) (Press release, Kite Pharma, JAN 28, 2020, View Source [SID1234553630]).

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The MAA is supported by data from the single arm, open-label, Phase 2 ZUMA-2 trial, which demonstrated an overall response rate of 93 percent, including 67 percent with complete response, as assessed by an Independent Radiologic Review Committee (IRRC) following a single infusion of KTE-X19 (median follow-up of 12.3 months). In the safety analysis, Grade 3 or higher cytokine release syndrome (CRS) and neurologic events were seen in 15 percent and 31 percent of patients, respectively. No Grade 5 CRS or neurologic events occurred. Detailed findings from this trial were recently presented during an oral session at the 61st American Society of Hematology (ASH) (Free ASH Whitepaper) Annual Meeting & Exposition in Orlando.

"Relapse rates in mantle cell lymphoma remain overwhelmingly high and there is a significant need for new therapies that may improve patients’ prognosis," said Ken Takeshita, MD, Kite’s Global Head of Clinical Development. "The EMA validation of our marketing application brings us closer to delivering on the promise of our industry-leading cell therapy development program, with the hope that we can bring KTE-X19 to appropriate patients in Europe as quickly as possible."

Kite submitted a Biologics License Application (BLA) for KTE-X19 to the U.S. Food and Drug Administration (FDA) on December 11, 2019 for the treatment of adult patients with relapsed or refractory MCL. KTE-X19 has been granted Breakthrough Therapy Designation (BTD) by the FDA and Priority Medicines (PRIME) by the EMA.

KTE-X19 is investigational and not approved anywhere globally. Its efficacy and safety have not been established. More information about clinical trials with KTE-X19 is available at www.clinicaltrials.gov.

About MCL

MCL is a rare form of non-Hodgkin lymphoma (NHL) that arises from cells originating in the "mantle zone" of the lymph node and typically affects men over the age of 60.

About ZUMA-2

ZUMA-2 is a single-arm, multicenter, open-label Phase 2 study involving 74 enrolled/leukapheresed adult patients (≥18 years old) with MCL whose disease is refractory to or has relapsed following up to five prior lines of therapy, including anthracycline or bendamustine-containing chemotherapy, anti-CD20 monoclonal antibody therapy and the BTK inhibitors ibrutinib or acalabrutinib. The objectives of the study are to evaluate the efficacy (60 patients) and safety (68 patients) after a single infusion of KTE-X19 in this patient population. The primary endpoint for the study is objective response rate (ORR). ORR in this trial is defined as the combined rate of complete responses and partial responses as assessed by an IRRC.

Secondary endpoints include duration of response, progression-free survival, overall survival, incidence of adverse events, incidence of anti-CD19 CAR antibodies, levels of anti-CD19 CAR T cells in blood, levels of cytokines in serum, and changes over time in the EQ-5D scale score and visual analogue scale score. The study is ongoing.

About KTE-X19

KTE-X19 is an investigational, autologous, anti-CD19 CAR T cell therapy. KTE-X19 uses the XLP manufacturing process that includes T-cell selection and lymphocyte enrichment. Lymphocyte enrichment is a necessary step in certain B-cell malignancies in which circulating lymphoblasts are a common feature. KTE-X19 is currently in Phase 1/2 trials in acute lymphoblastic leukemia (ALL), mantle cell lymphoma (MCL) and chronic lymphocytic leukemia (CLL).

Stem cells, CRISPR and gene sequencing technology are basis of new brain cancer model

On January 28, 2020 University of California reported that Using genetically engineered human pluripotent stem cells, University of California San Diego School of Medicine researchers created a new type of cancer model to study in vivo how glioblastoma, the most common and aggressive form of brain cancer, develops and changes over time (Press release, University of California at Los Angeles, JAN 28, 2020, View Source;scc012820.php [SID1234553647]).

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"We have developed stem cell models that are CRISPR-engineered to have tumor-associated driver mutations in glioblastoma, which harbor essentially all features of patient-derived tumors, including extrachromosomal DNA amplification," said co-senior author Frank B. Funari, PhD, professor in the Department of Pathology at UC San Diego School of Medicine and head of the Laboratory of Tumor Biology in the San Diego branch of the Ludwig Institute for Cancer Research.

"These models, or avatars as we call them, enable us to study human tumor development over long periods in vivo, which has not been feasible with patient-derived tissue samples which already harbor other genetic changes."

Reporting in the January 28, 2020 issue of Nature Communications, researchers used CRISPR editing to make precise mutations in an otherwise "normal" genome to create the genetic conditions that enable tumor development. The resulting avatars are unique in that they behave like a grade 4 glioma — a fast-growing type of tumor that starts in the glial cells of the brain — in their level of pathology, transcriptome signatures, engineered genetic alterations and evolution of genetic mutations, such as the emergence of extrachromosomal DNA and chromosomal rearrangements.

"The addition of single-cell RNA sequencing and computational tools enabled efficient analysis of big data to truly evaluate the surprising intra-tumor heterogeneity present in our avatars which replicates what is seen in patients samples," said co-senior author Gene W. Yeo, PhD, professor in the Department of Cellular and Molecular Medicine and the Institute for Genomic Medicine at UC San Diego and faculty member in the Sanford Consortium for Regenerative Medicine.

Existing mouse models work for testing drugs for specific mutations, but do not account for the diverse ways that tumors can develop. Human tissue samples do not allow for standardization in testing. This new avatar modeling system, said the authors, provides a platform for standardized studies on tumor biology and evolution.

"We can now test which mutations predicted by cancer genome projects are truly tumor-driving, and how they become invasive," said Yeo. "More importantly, these cancer avatars provide systematic, well-controlled opportunities for drug discovery."

Glioblastoma is highly malignant. Standard treatment is aggressive: surgery, followed by chemotherapy and radiation. Yet most tumors recur within six months. The two-year survival rate is 30 percent.

This avatar mimics the intra-tumor heterogeneity observed in people, making it a good option for detailed examination of tumor evolution and searching for therapeutic vulnerabilities based on driver genetics, said Furnari.

"Next steps include screening drugs, testing other mutations in adult and pediatric brain tumors as well as to evaluate if these approaches can model tumors in other tissues, such as the pancreas and lung," said Furnari.

STAND UP TO CANCER AWARDS 2020 LAURA ZISKIN PRIZE IN TRANSLATIONAL RESEARCH TO DRS. LEISHA A. EMENS AND XIANG ZHANG

On January 28, 2020 Stand Up To Cancer (SU2C) reported that it has awarded the 2020 Laura Ziskin Prize in Translational Research to two highly respected clinical investigators who will come together in a novel collaboration between leaders in breast cancer immuno-oncology and tumor immunology for research to further the availability of immune checkpoint inhibitors for breast cancer patients (Press release, SU2C, JAN 28, 2020, View Source [SID1234553614]). Dr. Leisha A. Emens, MD, PhD of UPMC Hillman Cancer Center, and Dr. Xiang Zhang, PhD of Baylor College of Medicine will share a $250,000 grant for their year-long research project which was awarded today at the 2020 SU2C Scientific Summit in Santa Monica.

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The Ziskin Prize is named after legendary Hollywood producer and Stand Up To Cancer Co-Founder Laura Ziskin, who lived with breast cancer for seven years before it took her life in 2011. Inaugurated in 2012, the prize was created with $1.1 million for this purpose in Ziskin’s will and has been awarded in 2012, 2014, 2015, 2018 and 2019.

"With their diverse backgrounds and complementary expertise, we’re confident that these two investigators will make great contributions to further develop therapies that could provide improved outcomes for breast cancer patients – and potentially reduce mortality rates," said Selection Committee co-chair John Glaspy, MD, MPH, professor. In granting the award, Selection Committee members included: co-chair Stephen Baylin, PhD, Johns Hopkins School of Medicine; Lewis Cantley, PhD, Sandra and Edward Meyer Cancer Center at Weill Cornell Medical College/Ronald P. Stanton Clinical Cancer Program at New York-Presbyterian; Gordon Mills, MD, PhD, OHSU Knight Cancer Institute; Carlos Arteaga, MD, Harold C. Simmons Comprehensive Cancer Center at UT Southwestern Medical Center; Ingrid Mayer, MD, MSCI, Vanderbilt University; Nancy Davidson, MD, Fred Hutchinson Cancer Research Center; Dennis Slamon, MD, PhD, Chief of the Division of Hematology/Oncology and executive vice chair for research for UCLA’s Department of Medicine; and Matthew Ellis, MB, BChir, BSc, PhD, FRCP, Baylor College of Medicine.

Dr. Emens is a professor of medicine in hematology/oncology, co-leader of the Hillman Cancer Immunology and Immunotherapy Program, and director of translational immunotherapy for the Women’s Cancer Research Center (WCRC) at UPMC. She is internationally recognized for her work in breast cancer immunotherapy. Clinically, she has developed a vaccine for breast cancer patients, and most recently led the development of atezolizumab from preclinical evaluation in human breast tumors to Phase 1 and Phase 3 clinical trials, resulting in an FDA approval for advanced triple negative breast cancer.

Dr. Zhang is a professor at the Baylor College of Medicine Breast Center whose research focuses on metastatic breast cancer where he has made significant contributions to the field. In the area of bone metastasis, he discovered the osteogenic niche that promotes early-stage bone colonization and invented a series of pre-clinical models and technologies to accelerate anti-metastasis drug discovery. In the area of tumor immunology and immunotherapies, he has made significant discoveries regarding the tumor microenvironment and its responses to checkpoint blockade therapies and has given a new understanding of how these interactions can affect the therapies.