TC BioPharm to Present at the H.C. Wainwright 24th Annual Global Investment Conference

On August 22, 2022 TC Biopharm (Holdings) PLC ("TC Biopharm" or the "Company") (NASDAQ: TCBP) (NASDAQ: TCBPW), a clinical stage biotechnology company developing platform allogeneic gamma-delta T cell therapies for cancer treatment, reported that Chief Executive Officer, Bryan Kobel will present a company overview at the H.C. Wainwright 24th Annual Global Investment Conference, on Monday, September 12th at 7:00 am (Press release, TC Biopharm, AUG 22, 2022, https://www.prnewswire.com/news-releases/tc-biopharm-to-present-at-the-hc-wainwright-24th-annual-global-investment-conference-301609516.html [SID1234618555]).

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A webcast of the presentation will be available on the Investor Relations page of TC BioPharm’s website. For more information or schedule a 1X1 meeting with management, please visit; View Source

Avenge Bio Announces Peer-Reviewed Publication on Preclinical Proof-of-Concept for LOCOcyte™ Platform Technology in Malignant Mesothelioma

On August 22, 2022 Avenge Bio, Inc., ("Avenge" or the "Company") a biotechnology company developing the LOCOcyte immunotherapy platform for the precision administration of potent immune effector molecules to treat solid tumors, reported a publication in the peer-reviewed journal Clinical Cancer Research describing the foundational, preclinical data establishing the efficacy and safety of pleural administered LOCOcyte for the treatment of pleural malignant mesothelioma (Press release, Avenge Bio, AUG 22, 2022, View Source [SID1234618554]). The manuscript, entitled "Activation of adaptive and innate immune cells via localized Interleukin-2 cytokine factories eradicates mesothelioma tumors," was published today and can be viewed on the Clinical Cancer Research website.

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Malignant mesothelioma and lung cancers which have metastasized to the pleural cavity remain particularly deadly with median survival times of less than a one year. Mesothelioma affects the organs that are lined by the mesothelium including the organs of the chest (pleura) and abdomen (peritoneum). It is a highly aggressive cancer and is essentially lethal in all cases. Despite recent advances in therapies to treat malignant mesothelioma, optimal and safe delivery remains a challenge. Current therapeutic options are of limited efficacy in both early and late-stage disease. Immunotherapies, including the use of PD-1 inhibitors, delivered systemically, have been shown to marginally extend patient survival. To overcome this challenge, a research team at Rice University led by Professor Omid Veiseh, Ph.D., has developed an innovative immunotherapy platform that enables engineered cells to produce immune-activating molecules, for a specified duration, within this fluid tumor microenvironment.

The Clinical Cancer Research manuscript details the LOCOcyte platform and its safety and efficacy in preclinical models. The human cells are engineered to produce murine immune cell signaling molecule interleukin-2 (IL2), a critical cytokine that initiates a robust localized immune response when administered into the pleural cavity of tumor-bearing mice that model advanced malignant mesothelioma. Overall, we observed a significant reduction of tumor burden in mice treated with IL2 monotherapy and complete eradication of tumor burden in mice treated with IL2 and an immune checkpoint inhibitor combination therapy.

"The continued occurrence of malignant mesothelioma necessitates the clinical assessment of new, effective treatments. Thus, the potential of the IL-2 cytokine factory for the treatment of malignant mesothelioma highlights the urgency of its evaluation in clinical trials," said Dr. Veiseh, Assistant Professor of Bioengineering at Rice University and a Founder of Avenge Bio.

Dr. Bryan Burt, Chief of the Division of Thoracic Surgery at Baylor College of Medicine, commented, "Pleural mesothelioma is a devastating malignancy that has traditionally defeated standard therapies. Whereas immune checkpoint blockade has recently demonstrated an encouraging signal in patients with unresectable disease, most patients still do not respond to therapy and systemic immune-related adverse events remain significant. Local delivery of a therapeutic can reduce toxicity by confining the immunostimulatory effects to local tumor microenvironment, highlighting a strong rationale for developing Avenge’s LOCOcyte platform."

Avenge Bio has an exclusive license from Rice University for this technology. In July 2022, Avenge announced that Food and Drug Administration ("FDA") cleared the Investigational New Drug ("IND") application for AVB-001 for the treatment of platinum resistance ovarian cancer. The Phase 1, multi-center clinical trial is expected to be initiated in the second half of 2022.

About LOCOcyte Platform
Our LOCOcyte allogeneic cell-based immunotherapy platform enables potent localized modulation of the immune system which also precipitates a systemic immune response, allowing us to treat previously intractable cancers. The technology leverage three unique advantages:

(1)Potent immune effector molecules are generated by synthetically engineering allogeneic cells creating a ready-to-use therapy,

(2) Therapy is localized in proximity to the primary tumor site and generates innate and adaptive immune response, and

(3) The immunomodulator trains the patient’s immune system generating a robust immune response that seeks and eradicates distal metastasis without systemic toxicity.

Pillar Biosciences Receives China National Medical Products Administration (NMPA) Approval for oncoRevealTM Dx Colon Cancer Assay

On August 22, 2022 Pillar Biosciences, the leader in Decision Medicine, developers and distributors of next-generation sequencing (NGS) tests which localize testing and reduce time to treatment initiation and overall testing costs, reported that its oncoRevealTM Dx Colon Cancer Assay has received approval from the China National Medical Products Administration (NMPA) (Press release, Pillar Biosciences, AUG 22, 2022, View Source [SID1234618553]). The IVD assay is now commercially available in China, the U.S., and Europe as a companion diagnostic (CDx) to identify patients with colorectal cancer whose tumors express wild-type KRAS status and may benefit from treatment with specific targeted therapies.

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"The oncoReveal Dx Colon Cancer Assay localizes NGS testing and efficiently provides a highly accurate genetic profile of KRAS mutations in metastatic colorectal cancer patients," said Randy Pritchard, Chief Executive Officer of Pillar Biosciences. "This approval is important for oncologists across China who need a more streamlined, efficient and accurate means of identifying the right therapy for their individual patients. By making testing more widely available, and enabling faster results, we can significantly reduce the amount of time it takes to initiate treatment and enable patients to more confidently continue along their life journey."

The oncoReveal Dx Colon Cancer Assay is a companion diagnostic test that identifies patients with metastatic colorectal cancer who have KRAS wild-type tumor status and may benefit from treatment with approved therapies, Erbitux (cetuximab) or Vectibix (panitumumab). The assay utilizes Pillar’s highly accurate and sensitive SLIMamp NGS testing technology to generate data that optimizes selection of precision therapies for cancer patients. This is the Company’s first NMPA approved diagnostic product. Pillar’s oncoReveal Dx Lung & Colon Cancer Assay previously received CE-IVD certification in Europe in April 2020 and U.S. Food and Drug Administration (FDA) Premarket Approval (PMA) in July 2021.

Bruker Introduces Enabling New Scientific Capabilities for Cell Biology and Pathobiology Research with High-Field NMR Innovations

On August 22, 2022 Bruker reported a new 8 mm 15N TROSY Cryoprobe for enabling novel NMR functional structural biology investigations into larger globular proteins and protein complexes (Press release, Bruker, AUG 22, 2022, View Source [SID1234618552]). The new technology also facilitates cell biology research into highly dynamic intrinsically disordered proteins (IDPs) or protein regions that often play key roles in signaling pathways via phosphorylation, e.g. in cancer. The new 8 mm 15N TROSY Cryoprobe provides twice the sensitivity of previous 5 mm detection, and 50% greater 13C sensitivity at 800 MHz. It allows researchers to obtain essential information in crowded IDP spectral regions for the unambiguous assignment of IDP backbone resonances.

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Dr. Haribabu (‘Hari’) Arthanari, Associate Professor in the Department of Biological Chemistry and Molecular Pharmacology at Harvard Medical School, and in the Department of Cancer Biology at the Dana-Farber Cancer Institute, stated: "We can now greatly expand the scientific scope of functional structural biology by high-field NMR with 15N-detected experiments to study non-deuterated protein systems, like disordered proteins or globular proteins, which can now be made in flexible eukaryotic expression systems. The new 8mm 15N TXO Cryoprobe holds promise to unleash the power of 15N-detection at high fields. I am very excited to see which previously inaccessible but important scientific and pathobiology questions this innovative NMR technology can address."

Bruker also announces the technology introduction of a novel 160 kHz Ultra-fast spinning Magic Angle Spinning (MAS) NMR probe for advancements in solid-state membrane protein, prion, and aggregates research. This new probe, which mechanically spins 160,000 times per second, provides a further significant resolution increase, and can record solids HCN NMR spectra in just tens of minutes. The significantly increased new capabilities of this 160 kHz 0.4mm MAS probe at high NMR fields may enable novel insights and discoveries in neurodegenerative diseases, like Parkinson’s and Alzheimer’s, and in other cell and disease biology fields.

Dr. Guido Pintacuda, CNRS Research Director and Director of the Lyon High-field NMR Center explained: "The new Bruker 160 kHz MAS HCN probe will push structural, cellular and disease biology research into the next phase of the solid-state NMR scientific evolution. Not only will this expand the diversity and molecular size range of biological systems such as membrane proteins, amyloid fibrils, prions, and aggregates amenable for analysis by solid-state NMR, but it will accelerate their investigation and increase the amount of information that can be extracted from these important biological systems."

Bruker is also very pleased to announce the installation and acceptance of the 1.2 GHz Avance NMR at University of Lille in France, which will be a part of the national infrastructure INFRANALYTICS. This first 1.2 GHz NMR in France will allow researchers in Lille, and from all over France, to advance their understanding of functional structural biology and advanced materials.

Professor Jean-Pierre Simorre, Research Director, and Deputy Director INC at CNRS, commented: "We are thrilled to have received our 1.2 GHz NMR system. The power and resolution of 1.2 GHz will provide the unique ability to study proteins in their natural state and examine their structural details, including binding and dynamics of molecular structures and complexes, for our fundamental cell biology and pathobiology research."

Professor Olivier Lafon at the University of Lille, and Director of Lille High-Field NMR Facility, expanded: "The 1.2 GHz NMR spectrometer will strongly improve the sensitivity and resolution for quadrupolar isotopes, such as 14N, 17O, 25Mg, 33S, 63Cu, and 67Zn, in materials and solid-state biomolecules. This will notably open new avenues for the study of dynamics, hydrogen bonds, disulfide bonds and metal centers of many metalloproteins, nucleic acids and carbohydrates."

Moreover, as announced at Euromar 2022, Bruker has received three orders for compact 1.0 GHz NMR systems from the RIKEN Center for Biosystems Dynamics Research in Yokohama, Japan, the Precision Medicine and Metabolism Lab at CIC bioGUNE, and the BioNMR Group at Universitat de Barcelona, both in Spain. The Ascend Evo 1.0 GHz NMR magnet utilizes hybrid high temperature superconductor (HTS) technology for operation at 4.2 Kelvin in single-story labs. The significantly reduced footprint, weight, and ceiling height, along with a 65% reduction in helium consumption, provides more structural biology principal investigators, universities, and research centers, as well as biopharma companies access to the sensitivity and resolution of GHz NMR. The 1.0 GHz system complements Bruker’s well-established Avance Neo 1.1 GHz and 1.2 GHz two-story 2 Kelvin NMR systems.

Bruker now offers combined bioTop and DynamicsCenter software to simplify and automate experimental setup, measurements, and processing for protein dynamics analysis. DynamicsCenter combines NMR assignments with 3D protein structures imported from crystallography or cryo-EM.

PanTher Therapeutics Awarded $14.2M from CPRIT to Advance Targeted, Localized and Sustained Cancer Treatment

On August 22, 2022 PanTher Therapeutics ("PanTher" or the "Company"), a clinical-stage oncology company developing next-generation targeted therapies for solid tumors, reported that received a $14.2 million grant from the Cancer Prevention and Research Institute of Texas (CPRIT) (Press release, PanTher Therapeutics, AUG 22, 2022, View Source [SID1234618551]). The funding will be used to expand clinical development through Phase 2 of PanTher’s lead investigational therapy, PTM-101, a minimally invasive, implantable treatment for non-metastatic pancreatic cancer that provides direct, sustained release of a known therapeutic agent at the tumor site.

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"Being selected for this highly competitive grant after thorough scientific, medical, regulatory and commercial due diligence, validates the clinical progress achieved so far as well as our mission. This award emphasizes the potential of PTM-101 to significantly benefit individuals with pancreatic cancer, while underscoring the urgent need for safe and effective options for hard-to-treat solid tumors," said Laura Indolfi, PhD, Chief Executive Officer and co-founder of PanTher Therapeutics.

PTM-101 is the first product to emerge from the company’s proprietary Sagittari platform, and it is currently being tested as a first-line treatment in a Phase 1 trial for locally advanced pancreatic cancer.

The Sagittari️ platform leverages interventional oncology procedures to design superior localized cancer treatments with adaptability to multiple solid tumor indications. The enabled customizable products are engineered for precisely transporting proven and novel therapeutic agents on target to attack cancer at the source.

"We are extremely grateful for the support from CPRIT and excited to build deeper collaborations with the local oncology and entrepreneurial communities with the establishment of our operations in Texas," continued Indolfi. "The funding will not only bring PTM-101 through the next phase of clinical development but will also allow us to accelerate the advancement of our novel Sagittari platform technology by expending internal resources to broaden our pipeline."

PanTher was one of nine companies working in the oncology space that received product development funding from CPRIT, with the grants totaling $64 million. The CPRIT also awarded nine prevention grants focused on increasing cancer-prevention and three recruitment grants aimed at enhancing cancer research efforts across Texas.