Aptevo Therapeutics Files Provisional Patent for Fifth Bispecific Antibody APVO711, Intended for the Treatment of Solid Tumors

On January 9, 2023 Aptevo Therapeutics Inc. ("Aptevo" or the "Company") (NASDAQ:APVO), a clinical-stage biotechnology company focused on developing novel immuno-oncology therapeutics based on its proprietary ADAPTIR and ADAPTIR-FLEX platform technologies, reported that the Company has filed a provisional patent with the U.S. Patent and Trademark Office (USPTO) pertaining to an anti-PD-L1 x anti-CD40 compound, APVO711, with the potential to fight a range of solid malignancies such as head and neck squamous cell carcinoma, melanoma, and carcinomas of the lung, gastrointestinal tract and colon (Press release, Aptevo Therapeutics, JAN 9, 2023, View Source [SID1234642041]). The Company plans to initiate pre-clinical studies this year.

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"Identifying new approaches to address the unmet needs of cancer patients is critical and APVO711 represents just such a new approach. This bispecific molecule targeting PD-L1 and CD40 is designed to function with new mechanisms of action and to synergistically induce a biological response. This is achieved by simultaneously engaging in two validated T cell activating mechanisms: 1) by blocking of PD-L1/PD-1 inhibitory pathway and 2) by enhancing T cell priming through activation of the stimulatory receptor CD40 on antigen presenting cells. APVO711 is designed to activate CD40 only in the presence of PD-L1 for an ideal safety profile." said Michelle Nelson, PhD, Director, Immunobiology at Aptevo. "Our goal in pre-clinical studies will be to continue to evaluate that APVO711 has the desired anti-tumor efficacy, mechanisms of action and safety profile we are looking for in our latest pipeline candidate."

"We are very pleased to announce that APVO711 is entering pre-clinical studies. This new compound expands our anti-cancer portfolio to five molecules and provides potential for another novel pathway to more effective cancer therapies in solid tumors," said Marvin L. White, President, and CEO of Aptevo Therapeutics. "As evidenced by clinical performance to date for APVO436, which has delivered compelling efficacy and safety data, we believe our additional ADAPTIR candidates, such as APVO711, have the potential to deliver similar outcomes."

Awarded: Innovate UK funding to design a new generation of cancer drugs

On January 9, 2023 Kuano Ltd reported grant funding from Innovate UK for a £540,000 Project toward Streamlined and Targeted Design of NOTUM Inhibitors as Colorectal Cancer Drugs (Press release, Kuano, JAN 9, 2023, View Source [SID1234639049]).

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Bowel cancer is a leading cause of death worldwide, with 17,000 deaths each year in the UK alone. Existing therapies suffer from the development of resistance. Kuano is looking to apply an innovative combination of quantum simulation and AI to produce a new generation of drugs targeting an enzyme (NOTUM) recently discovered to play a key role in cancer development. Like many diseases, a major cause of bowel cancer is malfunctioning or overactive enzymes – the chemical machines that accelerate chemistry within all living things.
Kuano demonstrated their platform can successfully reproduce existing drugs and have verified in the laboratory it can develop novel starting compounds for drug design. With this InnovateUK "Biomedical Catalyst 2022 Round 1: Industry-led R&D" grant Kuano will produce new cancer drug candidates that could represent a huge breakthrough in medical science and, ultimately, to society.

Kuano CEO, Vid Stojevic "The goal of Kuano is to develop a revolutionary quantum-led approach to drug discovery. I am very proud of the progress Kuano has made so far to validate our vision. It is exciting to have received InnovateUK support which will enable us to further develop our approach specifically for the colorectal cancer therapeutic area, paving the way to enable real world impact for colorectal cancer sufferers in the years to come."

Head of Health Technologies at Innovate UK, Samana Brannigan "Biomedical Catalyst funding will enable Kuano to implement an innovative combination of quantum simulation and AI to produce a new generation of drug with the potential to improve cancer treatment for colorectal cancer patients. The funding will deliver further growth for the UK Life Sciences Sector and lead to significant global opportunities for the company.

GNS Rebrands as Aitia to Focus on AI-Enabled Drug Discovery

On January, 2023 GNS, the leader in the application of causal AI and "Digital Twins" to discover and develop new drugs, announced today its rebranding as Aitia (pronounced "ay-tee-ah") (Press release, GNS Healthcare, JAN 9, 2023, View Source [SID1234638790]). Aitia, derived from the Greek word for causality, will focus on further leveraging its Gemini Digital Twins to discover the next generation of breakthrough drugs to improve outcomes for patients. Gemini Digital Twins are being used today to discover novel therapies and accelerate R&D in multiple myeloma, prostate cancer, Alzheimer’s Disease, Parkinson’s Disease, and Huntington’s Disease, with several more in development across oncology, neurodegeneration, and immunology.

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Aitia will partner with biopharma companies from the earliest stages of the discovery process through pre-IND. Aitia will also continue partnering with leading biopharma companies to simulate their drug candidates in patient cohorts derived from the Gemini Digital Twins.

"We are taking this important step in our evolution to leverage the exciting discoveries that are emerging from our Digital Twins" said Colin Hill, CEO and co-founder of Aitia. "These discoveries are now coming at an accelerated rate because of the power of our causal AI technology used to create the Digital Twins and the availability of rich multi-omic patient data. We are excited to continue to work with our current partners and with new partners to advance our discoveries further along the drug discovery process and eventually see these discoveries move into the clinic and to patients."

Boan Biotech’s First Investigational ADC, BA1301 for Injection, Approved for Clinical Trials in China

On January 09, 2023 Luye Pharma Group reported that BA1301 for injection, an innovative antibody-drug conjugate (ADC) candidate developed by its subsidiary Boan Biotech, has been approved for clinical trials by the Center for Drug Evaluation (CDE) of China’s National Medical Products Administration (NMPA) (Press release, Luye Pharma, JAN 9, 2023, View Source [SID1234638772]). This drug is intended for treating advanced solid tumors expressing Claudin 18.2, including advanced gastric cancer, gastroesophageal junction adenocarcinoma, and pancreatic cancer.

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Boan Biotech is committed to building a diverse portfolio of biologics developed on its innovative platforms for monoclonal antibodies, bispecific antibodies, and ADCs. The BA1301 for injection is Boan Biotech’s first novel ADC candidate to undergo clinical trials soon. The company employs C-Lock a site-specific conjugation technique from its partner Levena Biopharma, to conjugate a cytotoxic payload with a monoclonal antibody targeting Claudin 18.2. This directs the cytotoxic payload towards tumors by leveraging the targeting capability of the antibody. Such a design reduces the side effects of the cytotoxic payload and improves the therapeutic window while being able to kill cancer cells.

Preclinical efficacy studies show that the BA1301 for injection has an excellent internalization activity and a strong bystander killing effect, and that it has also demonstrated an exceptional inhibitory effect on tumor growth in tumor models with different levels of Claudin18.2 expression both in vitro and in vivo. The results of preclinical pharmacokinetic and toxicological studies show that the BA1301 for injection has a good safety profile, tolerability and stability in animals with no significant free cytotoxic payload released in plasma.

Binding to Claudin18.2, a high-potential anticancer target, BA1301 for injection aims to fulfill the huge unmet needs of cancer patients

According to the World Health Organization’s International Agency for Research on Cancer (IARC), China had about 4.57 million new cases of cancer in 2020, and the situation of gastrointestinal tumors was particularly concerning: the number of new cases and deaths of gastric cancer was around 480,000 and 370,000 respectively, with both numbers being nearly half of the global total for this disease, and for pancreatic cancer, the deadliest one among all cancers, both the number of new cases and the number of deaths were over 120,000 in China1.

The heavy disease burden is in contrast with the concerning status quo of treatment. The main treatment for advanced gastric and pancreatic cancer is palliative systemic chemotherapy, of which both the efficacy and the prognosis are very poor in general. In addition, available second-line treatments for advanced gastric and pancreatic cancer are limited, systemic chemotherapy is less specific, and the outcomes for patients are not as good as expected.

Claudin18.2 is a highly selective biomarker with limited expression in normal tissues but highly selective and stable expression in specific cancer tissues, especially gastrointestinal cancers such as gastric cancer and pancreatic cancer, and is involved in the proliferation, differentiation and migration of cancer cells. Research shows that Claudin18.2 is expressed in 70% of gastric cancer patients, 50% of pancreatic cancer patients, and 30% of esophageal cancer patients, making it a high-potential molecular target for anticancer drugs. Today, no drug targeting Claudin18.2 has been approved for marketing in the world. However, the recent success of a Phase III clinical trial for an investigational drug with the same target reinforced the industry’s confidence in developing drugs targeting Claudin 18.2. The BA1301 for injection is expected to improve the treatment outcomes for Claudin18.2-positive patients with gastric adenocarcinoma/gastroesophageal junction adenocarcinoma, pancreatic cancer or other cancers, and to provide a new treatment option for them.

With breakthroughs on its ADC platform, Boan Biotech has demonstrated the ability to innovate efficiently

ADCs are a new category of drugs. Known as "biological missiles", they direct small-molecule toxins towards tumors to kill their cells by leveraging the targeting capability of antibodies. And different drugs can be administered in combination to generate a synergy among different systems to attack target cancer cells precisely and effectively. Today, Boan Biotech has put into place an ADC platform covering the entire discovery and development process of ADCs. The BA1301 for injection is the first candidate developed by the company on its ADC platform. Employing the site-specific conjugation technique, the drug has demonstrated a good safety profile, as it is more homogeneous, and its small-molecule toxin isn’t easy to fall off.

Dr. Dou Changlin, R&D President and Chief Operating Officer of Boan Biotech, said: "Drugs targeting Claudin 18.2 have the potential to become novel anticancer therapies. Boan Biotech has developed candidates with different mechanisms of action in this field, to address a wide range of unmet needs for patients. The approval of the BA1301 for injection as our first ADC candidate for clinical trials has demonstrated the strength of our platform and our ability to innovate through efficient collaboration thanks to our multiple years of hard work. This has also paved way for us to develop more ADC products in the future. I believe our unique ADC platform will help to drive the development of more candidates in the future, to make our platform matrix and product portfolio more diverse, and to increase the company’s potential value."

Q2 2023 Quarter Ended Nov 30, 2022

On January 9, 2023 CytoDyn reported its second quarter for the fiscal year ended May 31, 2023 (Filing, 3 mnth, DEC 31, CytoDyn, 2022, JAN 9, 2023, View Source [SID1234630420]).

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