Quest Diagnostics To Speak At The 2020 Wells Fargo Virtual Healthcare Conference

On September 2, 2020 Quest Diagnostics Incorporated (NYSE: DGX), the world’s leading provider of diagnostic information services, reported that it is scheduled to speak at the Wells Fargo Virtual Healthcare Conference (Press release, Quest Diagnostics, SEP 2, 2020, View Source [SID1234564289]). Mark Guinan, Executive Vice President and CFO will discuss the company’s vision, goals and two-point strategy to accelerate growth and drive operational excellence, and the company’s current perspective on the impact of the COVID-19 pandemic. The presentation is scheduled for Thursday, September 10, 2020 at 1:20 p.m. Eastern Time.

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The presentation will be webcast live during the conference and will be available on the company’s investor relations page which can be accessed at ir.QuestDiagnostics.com. In addition, the archived webcast will be available within 24 hours after the conclusion of the live event and will remain available until October 10, 2020.

Sunesis Pharmaceuticals Announces 1-for-10 Reverse Stock Split

On September 2, 2020 Sunesis Pharmaceuticals, Inc. (Nasdaq: SNSS) reported that it has filed a Certificate of Amendment to its Amended and Restated Certificate of Incorporation to effect a 1-for-10 reverse stock split, effective as of 5:00 p.m. Eastern Time today (Press release, Sunesis, SEP 2, 2020, View Source [SID1234564288]). The reverse stock split was effected by Sunesis in accordance with the authorization, and within the split ratio range, adopted by Sunesis stockholders at the 2020 Annual Meeting of Stockholders held on June 16, 2020.

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The reverse stock split is intended to enable Sunesis to regain compliance with the $1.00 minimum bid price required for continued listing on the Nasdaq Stock Market LLC.

Sunesis is focused on the IND-enabling program for its first-in-class PDK1 inhibitor SNS-510 and is continuing to review strategic alternatives for the Company to maximize shareholder value.

At the effective time of the reverse stock split, every issued and outstanding ten shares of Sunesis’ pre-split common stock, par value $0.0001 per share, including shares subject to outstanding stock options and warrants and shares available for grant under Sunesis’ equity benefit plans, will automatically be combined into one share of Sunesis’ post-split common stock. The reverse stock split will affect all stockholders uniformly and will not affect any stockholder’s ownership percentage of Sunesis’ shares (except to the extent that the reverse stock split would result in some of the stockholders receiving cash in lieu of fractional shares). Stockholders will receive cash in lieu of fractional shares based on today’s closing sales price of Sunesis’ common stock as quoted on the Nasdaq Stock Market LLC. American Stock Transfer and Trust Company, Sunesis’ transfer agent, will provide instructions to stockholders regarding the process for exchanging their shares and stock certificates. Upon completion of the reverse stock split, there will be approximately 18.1 million shares of Sunesis’ common stock outstanding, excluding outstanding and unexercised stock options and warrants, subject to adjustment for fractional shares. In addition, Sunesis has convertible preferred shares outstanding which will be convertible into approximately 1.0 million post-split shares of common stock.

Additional information regarding the reverse stock split approved by stockholders can be found in Sunesis’ definitive proxy statement filed with the Securities and Exchange Commission on April 28, 2020.

RGENIX to Present at H.C. Wainwright 22nd Annual Global Investment Conference

On September 2, 2020 RGENIX, Inc., a clinical stage biopharmaceutical company developing first-in-class small molecule and antibody cancer therapeutics, reported that it has been selected to present at the H.C. Wainwright 22nd Annual Global Investment Conference (Press release, Rgenix, SEP 2, 2020, https://rgenix.com/rgenix-to-present-at-h-c-wainwright-22nd-annual-global-investment-conference/ [SID1234564287]). Rgenix will present at 12 P.M. EDT on September 16, 2020.

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To view this virtual presentation live, register for the event here.

Links to the live and archived versions of these presentations will also be available on Rgenix’s website within the News section.

City of Hope scientists use two powerful immunotherapies to eradicate solid tumors

On September 2, 2020 City of Hope scientists reported that have combined two potent immunotherapies — an oncolytic virus and chimeric antigen receptor (CAR) T cell therapy — to target and eradicate solid tumors that are otherwise difficult to treat with CAR T therapy alone, according to a new Science Translational Medicine study (Press release, City of Hope, SEP 2, 2020, View Source [SID1234564286]).

In preclinical research that could lead to a clinical trial for patients with intractable solid tumors, City of Hope scientists genetically engineered an oncolytic virus to enter tumor cells and force their expression of CD19 protein on their cell surface. Scientists were then able to use CD19-directed CAR T cells to recognize and attack these solid tumors.

CD19-CAR T cell therapy is approved by the U.S. Food and Drug Administration to treat certain types of blood cancers, namely B cell lymphomas and acute lymphoblastic leukemia. This new research may expand the use of CD19-CAR T cells for the treatment of patients with potentially any solid tumor.

"Our research demonstrates that oncolytic viruses are a powerful and promising approach that can be combined strategically with CAR T cell therapy to more effectively target solid tumors" said Saul Priceman, Ph.D., the study’s senior author and an assistant professor in City of Hope’s Department of Hematology & Hematopoietic Cell Transplantation.

"In addition, this therapeutic platform addresses two major challenges that make solid tumors so difficult to treat with immunotherapy. There are limited, established solid tumor targets that T cells can be redirected against with CARs," Priceman added. "Furthermore, solid tumors are surrounded by a brick wall — a so-called immunosuppressive tumor microenvironment. When a CAR T cell attempts to enter the tumor, survive, and kill cancer cells, it can’t effectively because of this barrier."

Yuman Fong, M.D., the Sangiacomo Family Chair in Surgical Oncology at City of Hope and a leading scientist who is developing oncolytic viruses for cancer treatment, added that the virus was able to break through that barrier.

"We designed this oncolytic virus to do what it does so well," Fong said. "It entered the cancer cell and used the cell’s own machinery to replicate itself, and engineer the cancer cells to express a truncated form of the well-known CAR T cell target, CD19."

Researchers first created an oncolytic virus (OV19t) in Fong’s lab to get into tumor cells and start producing truncated CD19 (CD19t). They did this successfully in triple-negative breast cancer lines, as well as in pancreatic, prostate, ovarian, and head and neck cancer, as well as brain tumor cells. CD19-CAR T cells were then combined with OV19t in vitro and in therapeutic studies in mice.
Researchers found several key findings.

"When we infected tumor cells with the virus, we observed the first signal that this may work. CD19t was being expressed by tumor cells much sooner than the virus was able to kill them, giving us a window of opportunity to be targeted by CD19-CAR T cells," said Anthony Park, Ph.D., the study’s lead author and a postdoctoral fellow in Priceman’s lab . "The combination of the two had a powerful, synergistic effect."

Researchers also showed that mice already cured of their cancer with the oncolytic virus and CAR T cell combination demonstrated prolonged protective anti-tumor immunity.

"The immune system built a memory response to the tumor," Park added. "Once it eradicated tumors, following the initial combination treatment, the mice were shielded against tumor recurrences."

Solid tumors are often immunologically cold, which means they are not typically responsive to therapies that use the body’s own immune system to fight cancer, Park said. Introducing the virus reversed the tumor’s harsh microenvironment, making it more receptive to receiving CAR T cell therapy.

The research demonstrates City of Hope’s collaborative approach to finding better immunotherapy cancer treatments. A few years ago, Priceman, Fong and Stephen J. Forman, M.D., leader of City of Hope’s Hematologic Malignancies Research Institute, met to brainstorm how they might combine their expertise, namely oncolytic virus and CAR T cell therapies, to target solid tumors.

"It was a simple concept but one that took many steps to get us to where we are today — we are now designing a clinical trial to test this combination in patients," said Priceman.

The trial would first test the safety of OV19t in patients with solid tumors. If that is found to be safe and effective, the oncolytic virus and CAR T cell therapy could then be tested in sequence. The trial is anticipated to start in 2022.

City of Hope, a recognized leader in CAR T cell therapies for blood cancers and solid tumors, has treated more than 500 patients since its CAR T program started in the late 1990s. The institution continues to have one of the most comprehensive CAR T cell clinical research programs in the world. It currently has 30 ongoing CAR T clinical trials, including CAR T trials for blood cancers and multiple solid tumor types such as primary and metastatic brain tumors, metastatic castration resistant prostate cancer, and more.

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Moffitt Researchers Identify Driver of Further Metastasis in BRAF Inhibitor Resistant Melanoma

On September 2, 2020 Moffitt Cancer Ctr reported that Targeted therapy with BRAF-MEK inhibitors is an effective treatment for patients with advanced melanoma that cannot be surgically removed or has spread to other areas of the body (Press release, Moffitt Cancer Ctr, SEP 2, 2020, View Source [SID1234564285]). However, many patients become resistant to the therapy, and this can often lead to further metastasis. Moffitt Cancer Center researchers who helped develop this type of combination therapy are now working to better understand what leads to this resistance in hopes of developing ways to overcome it.

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In a new article published in the Journal of Investigative Dermatology, Moffitt researchers identify erythropoietin-producing hepatocellular receptor A2 (EphA2) as a driver of metastasis and BRAF-MEK inhibitor resistance in melanoma.

EphA2 is a tyrosine kinase receptor that helps maintain a stable environment in normal cells. However, EphA2 is often overexpressed in many cancers and plays a critical role in its growth. Its exact function depends upon the signaling pathway: canonical and noncanonical. The canonical pathway inhibits cancer cell proliferation and acts as a tumor suppressor. The noncanonical pathway has the opposite effect, promoting tumor survival and metastasis.

The Moffitt team, in collaboration with scientists at Sanford Burnham Prebys Medical Discovery Institute, focused on the noncanonical pathway of EphA2. Using comprehensive mass spectrometry-based phosphoproteomics, the researchers mapped the signaling network driven by noncanonical EphA2 and found that it induces an amoeboid phenotype that enhances metastatic potential.

"This is important because an amoeboid phenotype enhances metastatic potential by helping to protect melanoma cells that have entered the blood stream from shear stress and allowing the cells to adhere to endothelial cells in other areas of the body," said Inna Smalley, Ph.D., study author and assistant member in the Cancer Physiology Department at Moffitt.

The research team further confirmed the findings by developing a mouse model using melanoma cells transduced with EphA2-S897E, the noncanonical pathway, and found a significantly higher number of metastases to the lungs.

"We hope that having a better understanding on what drives resistance to BRAF and BRAF-MEK inhibitor therapy and further metastasis will allow us to better understand the process of therapy escape and develop new treatment strategies for melanoma patients," said Keiran Smalley, Ph.D., lead study author and director of the Donald A. Adam Melanoma and Skin Cancer Center of Excellence at Moffitt.

This study was supported by the National Cancer Institute (K99 CA226679, R01 GM131374, P30 CA076292) and a Bankhead-Coley grant from the State of Florida (8BC03).