Puma Biotechnology to Present at Cowen’s Annual Health Care Conference

On February 28, 2020 Puma Biotechnology, Inc. (NASDAQ: PBYI), a biopharmaceutical company, reported that Alan H. Auerbach, Chairman, Chief Executive Officer, President and Founder of Puma, will provide an overview of the Company at 9:20 a.m. EST on Wednesday, March 4 at the Cowen and Company 40th Annual Health Care Conference (Press release, Puma Biotechnology, FEB 28, 2020, View Source [SID1234555003]). The conference will be held at the Boston Marriott Copley Place.

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A live webcast of the presentation will be available on the Company’s website at www.pumabiotechnology.com. The presentation will be archived on the website and available for 30 days.

Harbour BioMed Announces U.S. FDA Approval of IND for Its Next Generation anti-CTLA-4 Antibody, HBM4003, to Treat Cancer

On February 28, 2020 Harbour BioMed (HBM) reported U.S. Food and Drug Administration (FDA) approval of its Investigational New Drug (IND) application to begin clinical studies with HBM4003, its next generation anti-CTLA-4 antibody for the treatment of cancer (Press release, Harbour BioMed, FEB 28, 2020, View Source [SID1234555002]). The U.S. study builds on an initial ongoing trial in Australia. The trial will evaluate the safety, tolerability, pharmacokinetics, and anti-tumor activity of HBM4003 as a single agent in subjects with advanced solid tumors.

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"The IND approval is an important next step in our global program to develop this exciting molecule," said Dr. Jingsong Wang, Founder, Chairman and CEO of Harbour BioMed. "In preclinical studies, HBM4003 demonstrated potent anti-tumor activity based on a differentiated mechanism of action and a favorable safety profile. HBM4003 is the first in a portfolio of mono- and bi-specific antibodies based on our patented, heavy chain only (HCAb) technology against various immuno-oncology and immunology targets that are advancing toward clinical trials."

About HBM4003
HBM4003 is the fully human anti-CTLA-4 monoclonal heavy chain only antibody (HCAb) generated from Harbour Mice. HBM4003 shows enhanced antibody-dependent cell cytotoxicity (ADCC) killing activity and is extremely specific to CTLA-4High Treg cells in tumor tissues. The potent anti-tumor efficacy and differentiated pharmacokinetics with durable pharmacodynamic effect presents a favorable product profile. This novel and differentiated mechanism of action has the potential to improve efficacy while significantly reducing the toxicity of the drug.

Zimmer Biomet Holdings to Present at Raymond James & Associates’ 41st Annual Institutional Investors Conference

On February 28, 2020 Zimmer Biomet Holdings, Inc. (NYSE and SIX: ZBH), a global leader in musculoskeletal healthcare, reported that it will participate in Raymond James & Associates’ 41st Annual Institutional Investors Conference at the JW Marriott Grande Lakes in Orlando (Press release, Zimmer Holdings, FEB 28, 2020, View Source;associates-41st-annual-institutional-investors-conference-301013383.html [SID1234554997]). Suky Upadhyay, Executive Vice President and Chief Financial Officer and Keri Mattox, Senior Vice President, Investor Relations and Chief Communications Officer, will present for the Company on Monday, March 2, 2020, at 9:50 a.m. Eastern Time.

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A live webcast of the presentation can be accessed via Zimmer Biomet’s Investor Relations website at https://investor.zimmerbiomet.com.

John Theurer Cancer Center Launches Clinical Trial of Personalized Cancer Vaccine Using New Gene-Based Technology for High-Risk Melanoma

On February 28, 2020 John Theurer Cancer Center at Hackensack University Medical Center is the only site in New Jersey and one of just 17 in the country participating in a multicenter international Phase II study of an innovative personalized cancer vaccine being evaluated in combination with pembrolizumab immunotherapy in patients with melanoma that has been surgically removed but has a high risk of coming back (Press release, John Theurer Cancer Center, FEB 28, 2020, View Source [SID1234554996]). The hope is that the vaccine can prime a patient’s immune system to be more responsive to immunotherapy and reduce the risk of cancer recurrence. Utilizing a novel and potentially revolutionary gene-based technology, the vaccine is created by comparing the patient’s normal cell DNA sequence to that of their tumor and identifying tumor specific changes to the DNA. Once identified, the patient-specific, tumor-specific changes are turned into a messenger RNA construct to be used as a vaccine.

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Pembrolizumab belongs to a class of drugs called "checkpoint inhibitors," which have transformed the treatment of melanoma. It works by blocking a protein called PD-1 which normally shuts down the immune response. Cancer cells use PD-1 to hide from the immune system. Inhibiting PD-1 enables the immune system to find and kill cancer cells.

"Pembrolizumab and other checkpoint inhibitors have been shown to reduce disease recurrence among patients with high-risk melanoma that was surgically removed. However, in many patients, the cancer eventually comes back," explained Andrew L. Pecora, M.D., FACP, CPE, a nationally recognized hematologist/oncologist at John Theurer Cancer Center and associate dean, Technology and Innovation, Hackensack Meridian School of Medicine at Seton Hall University, who is a principle investigator (PI) of the study. "Reducing the rate of relapse would address a significant unmet medical need for these patients."

The study, "A Phase II Randomized Study of Adjuvant Immunotherapy with the Personalized Cancer Vaccine mRNA-4157 and Pembrolizumab versus Pembrolizumab Alone after Complete Resection of High-Risk Melanoma," is assessing a vaccine made by ModernaTX, Inc. called mRNA-4157. A personalized vaccine is made and given back to the patient to trigger the immune response.

John Theurer Cancer Center was also a study site for the Phase I clinical trial of the vaccine, which was assessed alone and in combination with pembrolizumab in patients with a variety of solid tumors. The results, which were presented at the 2019 Annual Meeting of the American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper), were promising — showing that mRMA-4157 was well tolerated, provoked an immune response, and resulted in clinical responses when given with pembrolizumab.

"Immunotherapy is revolutionizing cancer care, but challenges remain. This is a very exciting customized anticancer vaccine using a novel technology," noted Martin E. Gutierrez, M.D., director of Drug Discovery and the Phase I Unit, chief of Thoracic Oncology at John Theurer Cancer Center, and a PI of the Phase I study. "We are encouraged by the Phase I findings and are hopeful that the Phase II study results will show a similar positive outcome for these patients."

"Participation in groundbreaking studies such as these demonstrates John Theurer Cancer Center’s leadership in clinical research," added Andre Goy, M.D., MS, chair and executive director of John Theurer Cancer Center. "We are committed to offering our patients the latest medical advances and furthering progress in cancer care through clinical investigation."

"Hackensack University Medical Center is delivering cutting-edge cancer treatments options for our patients," said Ihor Sawczuk, M.D., FACS, president, Northern Region, chief research officer, Hackensack Meridian Health. "By utilizing gene-based technology, we are offering patients hope with a personalized cancer vaccine that can boost immune responses and reduce the risk of relapse for melanoma patients."

"Hackensack University Medical Center is advancing research and innovation to discover new treatment options for our patients," said Mark D. Sparta, FACHE, president and chief hospital executive, Hackensack University Medical Center and executive vice president of Population Health, Hackensack Meridian Health. "We look forward to seeing how this innovative vaccine and advances in immunotherapy will help us expand treatment options for patients with melanoma."

Carisma Therapeutics to Present at March Scientific and Investor Conferences

On February 28, 2020 Carisma Therapeutics Inc., a biopharmaceutical company focused on discovering and developing innovative immunotherapies, reported that the company will present at two conferences in March, 2020 (Press release, Carisma Therapeutics, FEB 28, 2020, View Source [SID1234554995]).

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Festival of Biologics USA, March 2-4, 2020: Steve Kelly, Chief Executive Officer, will present at the World Immunotherapy Congress on Monday, March 2, 2020, at 3:00 p.m. PST. The congress will be held at the Loews Resort Coronado in San Diego, CA.
Cowen and Company 40th Annual Healthcare Conference, March 2-4, 2020: Tom Wilton, Chief Business Officer, will present on Tuesday, March 3, 2020, at 5:00 p.m. EST. The conference will be held at the Marriott Copley Place in Boston, MA.
Immuno-Oncology Summit Europe, March 9-12, 2020: Michael Klichinsky, PhD, Co-Founder and VP, Discovery Research, will deliver a presentation entitled "CAR Macrophage Immunotherapy: A New Frontier for Innate Immunity" on Tuesday, March 10, 2020 at 1:55 p.m. GMT. The summit will be held at the Hilton London Canary Wharf in London, UK.