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).

Applied DNA to Present at H.C. Wainwright 22nd Annual Global Investment Conference on September 15

On September 2, 2020 Applied DNA Sciences, Inc. (NASDAQ: APDN) ("Applied DNA" or the "Company"), a leader in Polymerase Chain Reaction (PCR)-based DNA manufacturing that enables in vitro diagnostics, pre-clinical nucleic acid-based therapeutic drug candidates, supply chain security, anti-counterfeiting and anti-theft technology, reported that Dr. James A. Hayward, Chief Executive Officer, will participate virtually in the H.C Wainwright 22nd Annual Global Investment Conference on September 15 at 2:30 p.m. ET (Press release, Applied DNA Sciences, SEP 2, 2020, https://adnas.com/applied-dna-to-present-at-h-c-wainwright-22nd-annual-global-investment-conference-on-september-15/ [SID1234564282]).

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A live webcast of Dr. Hayward’s presentation will be available in the "IR Calendar" section on the Investor Relations page of the Applied DNA website at adnas.com.

Rain Therapeutics Announces Exclusive License to the Clinical-Stage MDM2 Inhibitor, DS-3032 (Milademetan) from Daiichi Sankyo

On September 2, 2020 Rain Therapeutics Inc. ("Rain"), a privately-held, clinical stage biotechnology company focused on targeted therapies for patients with cancer, reported it has licensed worldwide rights to a clinical stage, small molecule, oral MDM2 inhibitor, DS-3032 (milademetan) from Daiichi Sankyo Company, Limited (Press release, Rain Therapeutics, SEP 2, 2020, https://www.rainthera.com/rain-therapeutics-announces-exclusive-license-to-the-clinical-stage-mdm2-inhibitor-ds-3032-milademetan-from-daiichi-sankyo/ [SID1234564281]). Rain will re-designate the program as RAIN-32 .

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RAIN-32 is a potent and selective MDM2 inhibitor that has been evaluated in clinical trials for solid tumors and hematologic malignancies. The profile and dosing schedule of RAIN-32 may lend a differentiated tolerability profile, enabling longer-term therapy as compared to other MDM2 programs in development.

"We’re excited to add RAIN-32, a clinical program with the potential to significantly impact cancers characterized by MDM2 amplification or overexpression, to Rain’s pipeline of targeted cancer therapies," said Avanish Vellanki, cofounder and chief executive officer of Rain Therapeutics. "Daiichi Sankyo has done extensive work that we intend to build upon as we implement a biomarker-driven strategy to complete RAIN-32’s development."

MDM2 has emerged as a potentially valuable target for cancer therapies due to its inhibitory effects on p53, a critical tumor suppressor. Rain intends to evaluate RAIN-32 in multiple indications where patients demonstrate MDM2 gene amplification or overexpression, with an initial focus on liposarcoma, where two-thirds of patients display MDM2 amplification.

Robert Doebele, MD, PhD, cofounder of Rain Therapeutics, added, "We hope to pursue a rapid registrational path for RAIN-32 in a challenging tumor type that lacks effective therapies, and look forward to rationally developing RAIN-32 for additional oncology indications where MDM2 activity plays a central role."

Rain anticipates the presentation of clinical data from the ongoing Daiichi Sankyo clinical trial in patients with advanced solid tumors at an upcoming medical conference.

Rain has licensed global rights for all indications of RAIN-32. Deal terms from the license agreement were not disclosed.

About RAIN-32
RAIN-32 has been evaluated in patients with various solid tumors, acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). RAIN-32 also has been evaluated in continuous and intermittent dose schedules that may offer a differentiated tolerability profile as compared to other MDM2 programs.

Two clinical studies for RAIN-32 are ongoing, including a study evaluating the safety and efficacy of RAIN-32 in patients with liposarcoma and in patients with FLT3-ITD AML treated with RAIN-32 and the FLT3 inhibitor, quizartinib. In addition, multiple investigator sponsored studies are being conducted by MD Anderson Cancer Center (MDACC) as well as National Cancer Center Hospital (NCCH) in Tokyo, Japan.