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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Kronos Bio Announces Discovery Collaboration with Genentech to Advance Novel Therapies Against Transcriptional Targets in Oncology

On January 09, 2023 Kronos Bio, Inc., a company dedicated to transforming the lives of those affected by cancer, reported that it has entered into a discovery collaboration in the field of oncology with Genentech, a member of the Roche Group, focused on discovering and developing small-molecule drugs that modulate transcription factor targets selected by Genentech (Press release, Genentech, JAN 9, 2023, View Source [SID1234629876]).

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The partnership will allow Genentech to leverage Kronos Bio’s expertise to identify protein-protein interactions, genetic dependencies and gene expression signatures to better understand and target the oncogenic activity of transcription factors in cancer types of interest. Under the collaboration, researchers at the two companies will collaborate using Kronos Bio’s proprietary drug discovery platform, including the small molecule microarray (SMM) for hit finding, to build upon research conducted to date by Genentech.

"This, our first collaboration, brings together expertise from both companies with the goal of answering fundamental scientific questions about the biology of cancer that we hope will one day lead to the advancement of new clinical candidates," said Norbert Bischofberger, Ph.D., president and chief executive officer of Kronos Bio. "We are pleased to be able to leverage our unique platform to collaborate with Genentech to further Kronos Bio’s understanding of transcription-driven oncogenesis and ability to identify novel targets involved."

Kronos Bio will lead discovery and research activities to a defined preclinical point when Genentech will have the exclusive right to pursue further preclinical and clinical development and commercialization. Under the terms of the agreement, Kronos Bio will receive an upfront payment of $20 million and be eligible for additional payments, which could total up to $554 million, based on reaching certain milestones, including discovery, preclinical, clinical and commercial milestones, as well as tiered royalties on any potential products that are commercialized as a result of the collaboration.

"We are excited about the possibilities that this collaboration with Kronos Bio brings to further our understanding of complex scientific networks with the goal of bringing highly effective medicines to patients," said James Sabry, Global Head of Roche Pharma Partnering.

About Kronos Bio’s Discovery Engine
Kronos Bio is focused on targeting the activity of oncogenic transcription factors that have a well-defined and central role in driving particular types of cancer. The company leverages its expertise to map transcription regulatory networks, enabling the identification of protein-protein interactions, genetic dependencies and gene expression signatures of specific oncogenic transcription factors in cancers of interest. Utilizing these transcription regulatory network maps, the company relies on a number of tools, including its proprietary Small Molecule Microarray (SMM) to screen for new drug starting points.

AmMax Bio Enters into an Exclusive Option Agreement with Evopoint Biosciences to License a Next Generation Antibody Drug Conjugate (ADC) for the Treatment of Solid Tumors

On January 9, 2023 AmMax Bio, Inc. ("AmMax"), a private clinical-stage biopharmaceutical company developing innovative therapeutics in oncology, and Evopoint Biosciences Co., Ltd ("Evopoint"), a leading biopharmaceutical company applying its cutting-edge platform technologies to discover and develop innovative medicines, reported that AmMax has entered into an exclusive option with Evopoint for a worldwide license, excluding Greater China, for the development and commercialization of a novel ADC for treating solid tumors (Press release, AmMax Bio, JAN 9, 2023, View Source [SID1234626210]).

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With its proprietary linker-payload system and monoclonal antibody, this technology has demonstrated robust antitumor activity in multiple preclinical models which presents significant opportunities to treat many different types of cancer. The animal efficacy and toxicity studies also support a significantly widened therapeutic index (TI) that is expected to provide a much-improved efficacy and safety profile.

"AmMax’s mission is to develop and commercialize oncology therapeutics that have the potential to become the new standard of care," said Larry Hsu, Ph.D., Chairman & Chief Executive Officer of AmMax, "Today’s agreement with Evopoint underscores this commitment by adding a potentially best-in-class ADC program to our portfolio. We are excited to partner with Evopoint and, upon exercising the option, to move this highly differentiated drug candidate into patient studies in the second half of 2023."

"We are very pleased to enter into this agreement with AmMax," said Jason Meijie Le, Chief Executive Officer of Evopoint Biosciences. "Evopoint is dedicated to develop and deliver innovative medicines to physicians and patients. We are very impressed with AmMax’s therapeutic area expertise and proven track record in drug development and commercialization. We look forward to partnering with AmMax to advance this transformative product worldwide. This collaboration evidences the superiority of our product pipeline."

Under the exclusive option agreement, the parties have pre-negotiated licensing terms and will work together to complete the upcoming IND filing and design subsequent dose-escalating clinical studies.