Published UCLA and Spectrum Solutions Saliva Liquid Biopsy Research Highlights Signal Amplifying Ability and Clear Detection of Cancer Biomarkers

On July 26, 2022 Spectrum Solutions, LLC reported the publishing of findings from their research collaboration with the University of California at Los Angeles (UCLA) and Dr. David Wong, UCLA School of Dentistry (Press release, Spectrum Solutions, JUL 26, 2022, View Source [SID1234616965]). The project has successfully demonstrated a superior ability to detect circulating tumor DNA (ctDNA) from saliva. Specifically, amplified EGFR mutations associated with non-small cell lung cancer (NSCLC) using Spectrum’s saliva collection and preservation system with the Electric Field–Induced Release and Measurement (EFRIM) electrostatic platform.

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The BIO Journal is the first journal to provide comprehensive peer-reviewed coverage of biospecimen procurement, processing, preservation, and banking, including ethical, legal, and societal considerations. The published research, "Proficiency Testing of Epidermal Growth Factor Receptor Mutations Detection in Saliva Using Spectrum Saliva Collector (SDNA-1000) and Preservative Solution Detected by Electric Field-Induced Release and Measurement," Feng Li et al, can be found in the Ahead of Print section online and Manuscript ID: BIO-2022-0093 – VOLUME 20, ISSUE 4 / AUGUST 2022.

Most lung cancers (85 percent) fall into the category called non-small cell lung cancer (NSCLC). Though this form of lung cancer progresses more slowly than small cell lung cancer (SCLC), 40 percent of those living with NSCLC will have it spread beyond the lungs by the time it is diagnosed. Many advances in targeted treatments for lung cancer are based on the evaluation of three EGFR gene mutations. Current methods for diagnosis and monitoring include invasive tissue biopsies, which create clinical obstacles for ongoing mutation analysis and cancer treatment. The less invasive liquid biopsy options using free floating cell-free DNA (cfDNA) or circulating tumor DNA (ctDNA) in solid tumor cancers, have quickly become an important part of the screening, diagnosis and monitoring process for cancer patients.

"The ability to detect EGFR mutations using ctDNA enables a broad range of clinical applications for laboratory medicine such as the early detection of disease, practical applications of personalized treatments, predicting treatment response and monitoring resistance," said Rohit Gupta, Chief Medical Officer for Spectrum Solutions. "Proving it can be done using saliva is groundbreaking."

The ctDNA associated with NSCLC, termed ‘ultra-short’ ctDNA (usctDNA), is a third smaller in size than the average fragment. This has made it extremely hard to detect using current liquid biopsy technology, especially without additional amplification. Prior to this study, Wong’s team published on the successful detection of the same usctDNA EGFR mutations from both early and late-stage patients living with NSCLC in both blood and saliva. When paired with new technology developed at UCLA by Dr. Wong, known as EFIRM, study findings have demonstrated an impressive 14-fold amplification of detectable usctDNA from saliva collected and stabilized using Spectrum’s SDNA-1000 compared to raw or neat saliva. Additionally, after diluting the signal down to 10 percent of the original concentration, the team continued to see enhanced amplification benefits from the Spectrum device, leading scientists to believe detection of a single ctDNA fragment may now be possible.

"Achieving detectable concentrations of ctDNA in body fluids is not an easy task. The significance of successfully demonstrating this capability with saliva is the holy grail of liquid biopsy research," said Dr. David Wong, UCLA School of Dentistry. "The discovery delivers, for the first time, a noninvasive opportunity for detection and the ongoing ‘real-time’ understanding of somatic mutation activity to direct and redirect successful treatment strategies."

"Understanding how many face the likelihood of treatment resistance, it is actually life changing to know the results from this research collaboration with Dr. Wong and UCLA has real power to positively impact patient outcomes," said Steve Fanning, CEO of Spectrum Solutions. "For patients, the ability to use the self-collection of saliva empowers a new, safer, easier and pain-free era of detection and treatment innovation with real at-home remote care possibilities."

Affini-T Therapeutics Appoints Pioneering T Cell Therapy and KRAS Developer Dirk Nagorsen, M.D., as Chief Medical Officer

On July 26, 2022 Affini-T Therapeutics, Inc., a biotechnology company unlocking the power of T cells against oncogenic driver mutations, reported the appointment of Dirk Nagorsen, M.D., as the company’s Chief Medical Officer (Press release, Affini-T Therapeutics, JUL 26, 2022, View Source [SID1234616963]). Dr. Nagorsen previously served as Vice President Early Development and Therapeutic Area Head, Hematology & Oncology Early Development at Amgen, where he oversaw multiple groundbreaking programs including the first approved KRAS targeted treatment, Lumakras (sotorasib) and multiple T cell-based agents.

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"We are seeing rapid advances in both cell therapy and our ability to target oncogenic driver mutations commonly found in hard-to-treat solid tumors," said Dr. Nagorsen. "By combining the potency of T cells with synthetic biology and the specificity of T cell receptors, Affini-T’s team of world-class researchers and drug developers can fully realize the potential of oncogenic driver mutations as the solution to potentially cure patients with solid tumors. With this, I see the company at the forefront of a new chapter in precision immunotherapy, and I am proud to join as Chief Medical Officer."

"Having overseen development of the first approved KRAS targeting agent, Dirk’s pioneering work in the space and passion for discovering new cancer treatments will fuel Affini-T’s development of novel therapies for intractable solid tumors with oncogenic driver mutations," said Arjun Goyal, M.D., M.Phil., Co-founder and Managing Director Vida Ventures and Co-founder of Affini-T. "We look forward to Dirk’s leadership and contributions as we work together to efficiently advance Affini-T’s development strategy and bring impactful medicines to patients globally."

Dr. Nagorsen has contributed more than 20 years to the hematology and oncology fields, both in academia and industry. During the course of his 10 plus years at Amgen, he oversaw more than 30 oncology programs spanning from IND filings through drug approvals. He also served as the Global Development Leader for Blincyto (blinatumomab), the first CD3 bispecific T cell engager targeting CD19, and led his team to secure Amgen’s first breakthrough designation and first accelerated approval in 2014. Before joining Amgen, he served as a Senior Medical Director at Micromet, a German biotech, through its acquisition by Amgen in 2012. Dr. Nagorsen’s groundbreaking research has resulted in over 60 peer-reviewed manuscripts, including papers published in New England Journal of Medicine, Journal of Clinical Oncology and Lancet Oncology. Dr. Nagorsen earned his medical doctorate and his habilitation (second scientific degree, equivalent of a Ph.D.) in experimental medicine and tumor immunology from Charité University Medicine Berlin. He trained in internal medicine, hematology and oncology at the Free University Berlin Medical School, at the NIH Clinical Center Bethesda, Maryland and at Charité University Medicine Berlin.

"Dirk played a foundational role in the development of the first KRAS-targeted therapy that not only received FDA approval but did so within three years of the start of its Phase I trial," said Jak Knowles, M.D., Co-founder, President and Chief Executive Officer, Affini-T Therapeutics. "As we look to leverage our platform to make a meaningful impact for patients with solid tumors, we believe that Dirk is uniquely positioned to drive the development of our clinical programs. We are delighted to have Dirk join our team and look forward to advancing potentially curative therapies."

causaLens Partners With Mayo Clinic to Discover Biomarkers of Cancer Using Causal AI

On July 26, 2022 causaLens, the London deep tech company reported that delivering the future of AI, has utilized its Causal AI technology in an important step towards adopting non-invasive methods for screening and understanding cancer (Press release, causaLens, JUL 26, 2022, View Source [SID1234616962]). New research demonstrates that Causal AI enables reliable early detection of cancers based on easy-to-administer and cost-effective blood tests.

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Using a strictly data-driven approach, causaLens, which this year received investment from Dorilton Capital and Molten Ventures, discovered possible causal connections between the expression of genes and proteins and the manifestation and stage of colorectal cancer.

Colorectal cancer is the fourth most common cancer – with 147,950 cases annually – and one of the most lethal cancers – with 53,000 deaths per year.

At present, the only screening method used for colorectal cancer is colonoscopy, to identify and remove precursor lesions. However, this procedure is expensive and invasive, limiting reach for a type of cancer that is increasing by 2% a year among the under 50s, and requires ever-shorter screening intervals to prevent disease in higher-risk patients.

For these reasons, there is an urgent clinical need for techniques that can reliably detect early-stage colorectal cancers via non-invasive methods. The potential impact of causaLens’ research — undertaken in collaboration with academics from the Mayo Clinic, the prominent US medical research center — would be a significant improvement in the long-term prospects of patients with colorectal cancer.

causaLens is the pioneer of Causal AI — the only AI technology that is capable of discovering and reasoning with cause-and-effect relationships. Causal AI can root out spurious correlations in which two or more variables are associated but not causally related, due to either coincidence or the presence of a third, unseen factor.

The company has successfully delivered transformational outcomes across many sectors, from improving investment portfolio returns to mitigating supply chain disruptions and navigating public health crises.

Commenting on the company’s work in cancer research, Nicholas Chia, Assistant Professor of Biophysics, Mayo Clinic said:

"Causal AI is a fundamental scientific breakthrough and causaLens’ vision for Causal AI extends far beyond enterprise decision making. causaLens has the potential to disrupt a vast range of sectors and industries and has already demonstrated the value of its Causal AI technology in biological applications such as the discovery of cancer biomarkers"

Halozyme to Report Second Quarter 2022 Financial and Operating Results

On July 26, 2022 Halozyme Therapeutics, Inc. (NASDAQ: HALO) ("Halozyme") reported it will release its second quarter 2022 financial and operating results on Tuesday, August 9, 2022, following the close of trading (Press release, Halozyme, JUL 26, 2022, View Source [SID1234616961]).

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Halozyme will host a conference call on Tuesday, August 9, 2022 at 4:30 p.m. ET to discuss the results. The dial-in numbers are (888) 330-2408 for domestic callers and (240) 789-2703 for international callers. The conference ID number is 89853. A live webcast and replay of the conference call will be available online on the investor relations section of the Halozyme Therapeutics corporate website at www.halozyme.com.

Sarepta Therapeutics to Announce Second Quarter 2022 Financial Results and Recent Corporate Developments on August 2, 2022

On July 26, 2022 Sarepta Therapeutics, Inc. (NASDAQ:SRPT), the leader in precision genetic medicine for rare diseases, reported that it will report second quarter 2022 financial results after the Nasdaq Global Market closes on Tuesday, August 2, 2022 (Press release, Sarepta Therapeutics, JUL 26, 2022, View Source [SID1234616960]). Subsequently, at 4:30 p.m. E.T., the Company will host a conference call to discuss its second quarter 2022 financial results and to provide a corporate update.

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The event will be webcast live under the investor relations section of Sarepta’s website at View Source and following the event a replay will be archived there for one year. Interested parties participating by phone will need to register using this online form. After registering for dial-in details, all phone participants will receive an auto-generated e-mail containing a link to the dial-in number along with a personal PIN number to use to access the event by phone.