Athenex, Inc. to Report Fourth Quarter and Full Year 2019 Earnings Results on February 27, 2020

On February 6, 2020 Athenex, Inc. (Nasdaq: ATNX), a global biopharmaceutical company dedicated to the discovery, development, and commercialization of novel therapies for the treatment of cancer, reported that it will release fourth quarter and full year 2019 financial results on Thursday, February 27, 2020, before the market opens, and host a conference call and live audio webcast 8:00am Eastern Time to discuss the financial results and provide a business update (Press release, Athenex, FEB 6, 2020, View Source [SID1234573883]).

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To participate in the call, dial 877-407-0784 (domestic) or 201-689-8560 (international) fifteen minutes before the conference call begins and reference the conference passcode 13698005. The live conference call and replay can also be accessed via audio webcast at the Investor Relations section of the Company’s website, located at View Source

MD Anderson Announces New Approach to CAR-T Using Natural Killer Cells

On February 6, 2020 The University of Texas MD Anderson Cancer Center reported that it has developed a slightly different approach using a different type of immune cell called Natural Killer (NK) cells (Press release, MD Anderson, FEB 6, 2020, View Source [SID1234554065]). These cells target the cell-surface antigen CD19 and in a Phase I/IIa clinical trial, showed eight of 11 had a therapeutic response, with seven showing complete responses.

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The research was published in the New England Journal of Medicine. The seven patients showed no evidence of disease at a median follow-up of 13.8 months. There were no major toxicities observed.

"We are encouraged by the results of the clinical trial, which will launch further clinical studies to investigate allogeneic cord blood-derived CAR NK cells as a potential treatment option for patients in need," said Katy Rezvani, professor of Stem Cell Transplant & Cellular Therapy at MD Anderson and corresponding author of the study.

The new approach was led by Rezvani with MD Anderson’s CAR NK platform, support of the adoptive cell therapy (ACT) platform, Chronic Lymphocytic Leukemia Moon Shot and B-Cell Lymphoma Moon Shot, which are all part of MD Anderson’s Moon Shots Program.

CAR NK cells are allogeneic, which means they can be drawn from healthy patients rather than the cancer patient. This would be an off-the-shelf approach that would allow CAR NK cells to be manufactured and stored for immediate use. The current CAR-T therapies are individualized and take several weeks from drawing the patient’s T-cells to when they are prepared to be reinfused.

The NK cells in their technique are cultured from donated umbilical cord blood, then genetically engineered to express the appropriate CAR, which recognizes the specific cancers. They say these particular cells are "armored" with IL-15, a type of immune signaling molecule that is engineered to improve growth and survival of the cells. In this case, they were designed to target B-cell cancers.

In the trial, 11 patients received a single dose of the CD19 CAR NK cells, one of three different dose levels. Five patients had CLL and six had NHL. All the patients in the trial and received at least three previous therapies, with the maximum being 11 previous therapies. The first nine patients treated were partially matched by human leukocyte antigen (HLA), but the final two patients were treated with no HLA match.

"Due to the nature of the therapy, we’ve actually been able to administer it in an outpatient said," Rezvani said. "We look forward to building upon these results in larger multi-center trials as we work with Takeda to make this therapy available more broadly."

The CAR NK platform was licensed to Takeda Pharmaceutical Company in 2019. Takeda has exclusive rights to develop and commercialize up to four of the programs, including the CDK19 CAR NK cell therapy (TAK-007) and B-cell maturation antigen (BCMA)-targeted CAR NK cells.

MD Anderson and Takeda are now collaborating on launching a pivotal clinical trial for TAK-007 in 2021.

Botanical drug is shown to help patients with head and neck cancers

On February 6, 2020 UCLA reported phase I clinical trial, a new plant-based drug called APG-157 showed signs of helping patients fight oral and oropharyngeal cancers (Press release, University of California at Los Angeles, FEB 6, 2020, View Source;bdi020620.php [SID1234554063]). These cancers are located in the head and the neck.

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APG-157 is made up of multiple compounds produced by plants, including curcumin. UCLA Jonsson Comprehensive Cancer Center researchers found that treatment with this botanical drug resulted in high concentrations of curcumin and its byproducts circulating in the blood and absorbed by tumor tissues within three hours after being taken orally.

APG-157 reduced the concentration of cytokines — proteins involved in inflammation — in the saliva when administered to cancer patients. The therapy also reduced the relative abundance of Bacteroides species, a group of gram-negative bacteria. Gram negative refers to a group of dangerous bacteria that have an outer layer which hides them from the immune system. The relative abundance of gram-negative bacteria compared to the presence of other types of bacteria is correlated with oral cancer.

APG-157 also resulted in the expression of genes that are associated with attracting immune system T cells to the tumor area. This therapy could have a beneficial effect when used in combination with immunotherapy drugs that help immune system T cells recognize and kill tumors.

The treatment did not have any adverse effects on the study’s participants.

BACKGROUND

Cancers of the head and neck account for 4% of all cancers. About 650,000 new cases are reported each year around the world. People with advanced head and neck cancers have a low survival rate and current treatment options such as surgery, radiation and chemotherapy can have adverse effects. Therefore, more effective and less toxic therapies are needed to help improve the quality of life and outcome for those with these cancers.

APG-157 is a botanical drug developed under the FDA’s Botanical Drug Guidance, which includes requirements for production of plant-based therapies that are marketed as prescription medications. The drug is made up of botanical compounds including curcumin from the Curcuma longa plant, which is commonly referred to as turmeric and is a member of the ginger family.

Curcumin is one of the medicinally active or therapeutic molecules that has been tested as a possible treatment to help fight multiple cancers because it is an antioxidant that reduces swelling and inflammation. However, there is poor absorption into the bloodstream when curcumin is taken orally. In this study, UCLA researchers found that when APG-157 is taken through oral mucosal absorption, patients have high levels of curcumin circulating in their blood and absorbed by cancer tissues.

METHOD

UCLA researchers conducted the study of APG-157 comparing 12 people who had oral and oropharyngeal cancer with a control group of 13 people who did not have cancer. The reason both the people with cancer and without cancer were part of the study was to show that the drug was not toxic to either people with cancer or those without cancer.

The medication was given each hour for three hours and was delivered as a lozenge that slowly dissolved in the mouth. Blood and saliva samples were collected beforehand — each of the three hours the medication was administered — and 24 hours after the last dosage. The medication was given to 12 people (some who had cancer and some who did not) and a placebo was given to 13 people. Blood and electrocardiogram tests did not show increased toxicity in the people who took the active medication in comparison with the people who took the placebo, regardless of whether they had cancer or not.

For the cancer patients who took the medication, there was a decrease in Bacteroides and an increase in T cells in the tumor tissue as compared to cancer patients who took the placebo. Neither the subjects nor the investigators knew whether the drug or a placebo was given when reviewing the blood and saliva test results of the blinded study.

IMPACT

APG-157 is a botanical drug that has low toxicity. It works effectively to reduce inflammation that contributes to the growth of cancer cells. It also attracts T cells to the tumor micro-environment. When used in combination with immunotherapy drugs, APG-157 might have the ability to make the immune system more effective in attacking head and neck cancers. With potential to inhibit the growth of Bacteroides species, APG-157 could also improve cancer therapy through oral microbial changes.

AkesoBio Files for $300 Million Hong Kong IPO to Develop Antibody Portfolio

On February 6, 2020 AkesoBio, a Zhongshan novel drug discovery and development biopharma, reported that it filed for a $300 million Hong Kong IPO to develop its portfolio of novel mono- and bi-specific antibodies (Press release, Akeso Biopharma, FEB 6, 2020, View Source [SID1234553999]). The company has built a portfolio of 18 mAbs that are in either CMC or clinical stages of development for oncology, inflammation, autoimmune and cardiovascular diseases. In general, Akeso develops bispecific antibodies using a PD-1 antibody as a backbone. Late last year, Akeso Biopharma closed a $150 million Series D round of financing led by Loyal Valley Capital and Sino Biopharm.

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PENTIXAPHARM Secures € 15 Million Series A Financing to Develop CXCR4-Targeted Theranostics

On February 6, 2020 PentixaPharm reported to have secured € 15 million in a series A financing round led by ELSA Eckert Life Science Accelerator (Press release, PentixaPharm, FEB 6, 2020, View Source [SID1234553988]).

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PentixaPharm GmbH, a joint venture of Scintomics GmbH and 1717 Life Science Ventures GmbH, is committed to develop PentixaFor and PentixaTher as a theranostic radiopharmaceutical pair, specifically targeting the CXCR4-receptor expressed in most fast progressing diseases, particularly malignant cancers. Funding is dedicated for a phase II trial of the imaging compound PentixaFor and for a phase I trial of the therapeutic compound PentixaTher in Central Nervous System (CNS) Lymphoma while supporting proof-of-concept studies in various other indications.

Interviews:
"With the renowned expertise of the PentixaPharm team, the company is well positioned to bring the lead-compounds PentixaFor and PentixaTher with an effective clinical development program to the next level. We are thrilled to accompany this venture.", says Phillip Eckert, Responsible Programme Manager and Partner at ELSA.

"Scintomics is very excited about this new partnership marking another important milestone towards a strong positioning of PentixaPharm as radiopharmaceutical development specialist", comments Saskia Kropf, CEO of Scintomics. Prof. Hans-Jürgen Wester, founder of Scintomics, adds: "We are enthusiastic by this round A financing to advance the CXCR4 program. Preclinical and clinical data so far have demonstrated encouraging evidence and good potential for targeted cancer therapies. Now with the experienced development team of PentixaPharm, we are sure to quickly establish this theranostic approach towards meaningful clinical trials."

"We are delighted that in ELSA we have found a strong financing partner with an outstanding expertise in the radiopharmaceutical field. The proceeds of the series A financing will enable us to bring a new treatment for CNS Lymphoma, up to today a disease with limited treatment options, a little closer to patients in need", adds Anna Steeger, Co-founder of 1717 LSV GmbH and CEO of PentixaPharm.