Anavex Life Sciences to Participate in the BTIG Virtual Biotechnology Conference 2021

On August 4, 2021 Anavex Life Sciences Corp. ("Anavex" or the "Company") (Nasdaq: AVXL), a clinical-stage biopharmaceutical company developing differentiated therapeutics for the treatment of neurodegenerative and neurodevelopmental disorders including Alzheimer’s disease, Parkinson’s disease, Rett syndrome and other central nervous system (CNS) disorders, reported that Christopher U. Missling, PhD, President and Chief Executive Officer of Anavex, will participate in a fireside chat in the BTIG Virtual Biotechnology Conference 2021 on Tuesday, August 10, 2021 at 9:30 a.m. EDT (Press release, Anavex Life Sciences, AUG 4, 2021, View Source [SID1234585724]).

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Webcast for the conference will be available in the Investors section under "Events" of the Anavex corporate website at www.anavex.com. To listen to the live event, please contact a BTIG representative with interest.

EQRx and AbCellera Announce Collaboration to Accelerate the Advancement of New Innovative Medicines

On August 4, 2021 EQRx, a company committed to developing and delivering important new medicines at radically lower prices, and AbCellera (Nasdaq: ABCL), a technology company with a centralized operating system for next-generation antibody discovery, reported a collaboration agreement for the discovery and development of therapeutic antibodies (Press release, EQRx, AUG 4, 2021, View Source [SID1234585740]). The collaboration will leverage AbCellera’s AI-powered antibody discovery technology to search and analyze natural immune responses to identify novel antibody drug candidates for multiple targets. The partnership, which spans several therapeutic areas, will help to rapidly expand EQRx’s early-stage pipeline of novel medicines. The deal also includes the option for additional investment from AbCellera at progressive stages of preclinical development, clinical development, and commercialization in exchange for an increased share of product sales. The initial programs will focus on targets in oncology and immunology.

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"This collaboration with AbCellera represents another important step to continue to expand our portfolio as we seek to lead the way in the future of affordable, accessible and high-impact medicines," said Carlos Garcia-Echeverria, Ph.D., chief of Rx creation at EQRx. "AbCellera’s operating system for antibody discovery addresses each step in the process to dramatically improve the cycle time, cost, and probability of success, and we look forward to working together to advance unique clinical candidates against key disease targets."

"AbCellera exists to create value by connecting technology with innovation of all kinds – innovation in biology, in new drug modalities, and in new commercial models. We’re proud to partner with EQRx on their bold mission to reimagine drug development and bring medicines to patients faster and at lower cost," said Carl Hansen, Ph.D., CEO of AbCellera. "This partnership is yet another example of how we can apply our business model, creating greater value and alignment through deals that include the option to invest in programs."

Immunovia, Inc. Receives Approval to Begin Testing Patients for Pancreatic Cancer with the IMMray™ PanCan-d Test

On August 4, 2021 Immunovia AB (publ) ("Immunovia"), a diagnostic company that develops highly accurate blood tests for the early detection of cancer and autoimmune diseases, reported that Immunovia, Inc. has received final approval to begin patient testing for the IMMray PanCan-d test – the first blood test on the market dedicated to the early detection of pancreatic cancer (Press release, Immunovia, AUG 4, 2021, View Source [SID1234585760]). This approval was received from the Massachusetts Department of Public Health on August 3, 2021. Immunovia, Inc. received its CLIA Certificate of Registration on June 21, 2021 (CLIA Number: 22D2227265). As a result, Immunovia, Inc. can immediately begin selling the IMMray PanCan-d test for early detection of pancreatic cancer in the US exclusively through their laboratory in Marlborough, Massachusetts.

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"We are extremely pleased to have achieved this important milestone and to be able to launch the first non-invasive, highly accurate blood test that can help detect pancreatic cancer in early stages. The IMMray PanCan-d test meets a huge clinical need and our ambition is to make the test available to individuals in all the high-risk groups for pancreatic cancer. As a first step, we will launch the test for the familial/hereditary high-risk group," said Patrik Dahlen, Immunovia’s CEO.

"With the Massachusetts State approval, we are excited to be the first to offer commercial testing for individuals at high risk for pancreatic cancer using the IMMray PanCan-d test," said Thomas King, MD, PhD, Medical Director of Immunovia, Inc.

The IMMray PanCan-d test is a laboratory developed test (LDT) that will be the first blood test on the market dedicated to the early detection of pancreatic cancer. By recognizing biomarker signatures, or signs of the disease in the blood, the IMMray PanCan-d test has the potential to significantly increase the survival of patients by detecting pancreatic cancer earlier, when surgical resection is possible.

Celyad Oncology Reports First Half 2021 Financial Results and Recent Business Highlights

On August 4, 2021 Celyad Oncology SA (Euronext & Nasdaq: CYAD) (the "Company"), a clinical-stage biotechnology company focused on the discovery and development of chimeric antigen receptor T cell (CAR T) therapies for cancer, reported an update on its financial results and recent business developments for the fiscal quarter ended June 30, 2021 (Press release, Celyad, AUG 4, 2021, View Source [SID1234585924]).

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"We continue to blaze a path forward by developing new technologies to advance allogeneic CAR T therapies, including our proprietary shRNA platform for allogeneic CAR T production and ‘armored’ CAR capabilities with co-expression of secreting cytokines, starting with IL-18. The innovations we are making through our clinical development pipeline and new technologies were the focus of our R&D day last month. This is an exciting time in our Company’s history as we plan for a steady stream of milestones in the second half of 2021," commented Filippo Petti, Chief Executive Officer of Celyad Oncology. "We plan on announcing multiple clinical updates in the next six months that are expected to help further the progress of our lead programs and proprietary shRNA platform for the development of next-generation allogeneic CAR Ts."

Second Quarter 2021 and Recent Business Highlights

•Dr. Charles Morris was appointed as Chief Medical Officer in April 2021.
•Preliminary data from the Phase 1 IMMUNICY-1 trial of CYAD-211 for the treatment of r/r MM were announced at the European Hematology Association (EHA) (Free EHA Whitepaper) 2021 Virtual Congress.
•Research & Development Day held on July 20, 2021, during which the management team provided:
•Updates on the allogeneic CAR T clinical candidates CYAD-211 and CYAD-101.
•Highlights from the latest research from its proprietary shRNA platform, including the introduction of CYAD-203 – a novel allogeneic, IL-18-armored CAR T candidate for solid tumor now in IND-enabling studies.
•Acquisition of an exclusive license from the Moffitt Cancer Center for an antibody directed to Tumor-associated glycoprotein (TAG-72), which will form the basis of a T cell engager to be used with our shRNA platform technology.
Pipeline Update

CYAD-101 – Allogeneic TIM-based NKG2D CAR T for mCRC

CYAD-101 is the Company’s first-in-class, allogeneic CAR T candidate engineered to co-express a chimeric antigen receptor (CAR) based on the NKG2D receptor and the novel inhibitory peptide TCR Inhibitory Molecule (TIM).

•To the Company’s knowledge, CYAD-101 is the first investigational allogeneic CAR T candidate to generate evidence of clinical activity for the treatment of a solid tumor indication. This is based on data reported from the dose-escalation segment of the alloSHRINK Phase 1 trial evaluating CYAD-101 following FOLFOX (combination of 5-fluorouracil, leucovorin and oxaliplatin) preconditioning chemotherapy for the treatment of advanced metastatic colorectal cancer (mCRC).
•CYAD-101 following FOLFOX preconditioning chemotherapy was observed to be well-tolerated with no evidence of Graft-versus-Host Disease (GvHD). In addition, two of 15 patients from the dose-escalation segment of the alloSHRINK trial achieved a confirmed partial response (PR). Median progression-free survival (mPFS) and median overall survival (mOS) from the dose-escalation segment was 3.9 months and 10.6 months, respectively

Biotech Company Looking to Detect HCC Early With Liquid Biopsy Based on Microbiome

On August 4, 2021 Micronoma, a San Diego company, reported its technology picks up signs of very early cancer from disrupted microbiome (Press release, Micronoma, AUG 4, 2021, View Source [SID1234585674]).

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Many researchers and companies are chasing the dream of detecting biomarkers of solid tumors in the blood, either to guide treatment, discover the cancer at an earlier, more treatable phase, or both. Liquid biopsies, as they are called, typically depend on finding a molecular signature of the cancer or some fragment of its DNA. Some liquid biopsy products are already approved and on the market.

Micronoma, a San Diego biotech company, is taking a different approach. The company is developing a technology designed to detect disruptions in the body’s microbiome — that vast array of bacteria and other organisms that inhabit the human body — caused by cancer. Micronomoa says its microbiome-based strategy will detect cancer at an earlier stage than other liquid biopsies.

The company announced recently that it is collaborating with researchers at the University of New South Wales in Australia on an effort to adapt its approach to early detection of liver. The collaboration is getting a boost from the Australian government in the form of a $4 million grant. Micronoma had previously focused on lung cancer, and its website talks about the advantages its technology has over low-dose CT scans for lung cancer screening.

Micronoma says its technology, which uses machine learning, can examine thousands of microbiome plasma features to discover, validate, and translate microbial-derived biomarkers for the early detection of hepatocellular carcinoma (HCC), the most common type of liver cancer, Micronoma said in a news release.

"The process is designed to improve the chances of survival of HCC patients and make effective risk disease stratification possible by discovering the disease in its earliest stages," Micronoma CEO Sandrine Miller-Montgomery told Managed Healthcare Executive.

HCC has a low overall 5-year survival rate (below 20%), primarily because themajority of patients are diagnosed at a late stage of the disease, Miller-Montgomery noted. "While HCC is still very deadly at stage 1 (the five-year survival rate is 34%) detection in stage 1 would still enable saving a significant number of lives," she said.

The cost savings to the overall healthcare system when the novel liquid biopsy detection method is implemented "will be huge, because early-stage treatment is significantly cheaper and more efficient than later stage treatment," Miller-Montgomery added.

The liquid biopsy diagnostic field is developing rapidly. Earlier this year, the FDA granted a Breakthrough Device designation for Bluestar Genomic’s proprietary noninvasive pancreatic cancer detection test in patients with new-onset diabetes.

Meanwhile, using a 400ul plasma sample, Micronoma’s initial preliminary test can detect next generation sequencing (NGS) microbial signatures that are a telltale sign of HCC, even in the earliest stages of the disease, Miller-Montgomery explained.

Micronoma’s method investigates signals from microbial signatures in the blood, which come from multiple sources, including the tumor itself and other locations, such as the GI tract.

After its research with UNSW is completed, it should take around two years for the technology to be commercially available. Micronoma is first prioritizing commercialization in the U.S. "but will work hard to expand our reach internationally, with Australia being top of the list.," Miller-Montgomery said