New CLTX CAR Technology Patent Protection in India and Israel

On April 27, 2023 Chimeric Therapeutics (ASX:CHM, "Chimeric" or the "Company"), the only ASX-listed clinical stage cell therapy company, reported that the Indian Patent Office has issued a patent covering certain applications of chimeric antigen receptor (CAR) technology using chlorotoxin (CLTX), including Chimeric’s clinical-stage CAR T asset CHM 1101 and preclinicalstage CAR NK asset CHM 1301 (Press release, Chimeric Therapeutics, APR 28, 2023, View Source [SID1234630605]).

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The India patent has been granted under patent number IN 424963, entitled "Chimeric antigen receptors containing a chlorotoxin domain."

In addition, the Israel Patent Office has issued an Official Notification Prior to Acceptance, a notice of allowance, for application IL 258670.

Chimeric holds the exclusive worldwide license to develop and commercialize IN 424963, IL 258670, and related patent applications filed in other global territories. Chimeric’s CEO and Managing Director Jennifer Chow said: "We are delighted to have patent protection granted for CLTX CAR therapies in India and shortly in Israel as we continue to expand the robust intellectual property portfolio underpinning our CLTX CAR pipeline assets."

About CHM 1101:

CHM 1101 (CLTX CAR T) is a first in class CAR T therapy that has the potential to address the high unmet medical need of patients with recurrent or progressive glioblastoma, patients who have a poor prognosis, with limited treatment options and a median survival of less than 1 year (Gallego. Curr Oncol, 2015).

CHM 1101 cells uniquely utilize chlorotoxin (CLTX), a 36-amino acid peptide derived from deathstalkerscorpion venom, as the tumour-targeting component of the chimeric antigen receptor (CAR). In preclinical models, CHM 1101 CAR T cells have been shown to bind more broadly and specifically to GBM cells than other targeting domains like EGFR, HER-2 or IL-13. CHM 1101 cells also demonstrated potent antitumor activity against glioblastoma while not exhibiting any off-tumor recognition of normal human cells and tissues, indicating a potentially optimal safety and efficacy profile.

CHM 1101 is currently being studied in an ongoing phase 1A clinical trial in recurrent / progressive glioblastoma at City of Hope Cancer Centre in California. Outcomes from the initial two dose levels of the Phase 1A trial have been previously presented and demonstrated patient safety with a disease stability rate of approximately 70%.

Generate:Biomedicines and MD Anderson Enter Co-Development and Commercialization Agreement to Accelerate Novel Protein Therapeutics for Oncology Using Generative AI

On April 27, 2023 Generate:Biomedicines and The University of Texas MD Anderson Cancer Center reported a strategic collaboration to jointly discover and co-develop protein therapeutics for up to five oncology targets in advanced cancers, including small-cell and non-small-cell lung cancer (Press release, Generate Biomedicines, APR 27, 2023, View Source [SID1234649864]).

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Under the co-development and commercialization agreement, MD Anderson and Generate:Biomedicines will each contribute toward creating optimized, potentially best-in-class therapeutics that can rapidly advance into proof-of-concept clinical trials. The agreement combines Generate:Biomedicines’ integrated machine-learning capabilities and experimental/​wet lab capabilities – which are powered by The Generate Platform – with MD Anderson’s clinical research expertise and the translational research and drug development capabilities of the Translational Research to AdvanCe Therapeutics and Innovation in Oncology (TRACTION) platform.

"Together with Generate:Biomedicines, we aim to leverage rapid advancements in generative AI to develop new medicines that are purpose-built for those who do not benefit from existing treatments or who have drug-resistant cancers requiring new options," said Timothy Heffernan, Ph.D., vice president of Oncology Research for TRACTION at MD Anderson. ​"By joining The Generate Platform with our integrated translational research and drug development approach, we hope to successfully scale drug discovery and development in a way that has eluded traditional trial-and-error methods."

By tapping into the programmability and scalability of The Generate Platform, researchers within TRACTION and across the MD Anderson research enterprise will accelerate the pace of drug development and inform clinical translation. TRACTION is a core component of MD Anderson’s Therapeutics Discovery division that deploys a fully integrated translational biology engine to overcome traditional challenges in oncology drug discovery.

"Our collaboration with MD Anderson is an embodiment of innovative and cooperative research purposed to maximize the clinical impact of new therapeutics in oncology," said Generate:Biomedicines’ Chief Medical Officer, Alex Snyder, M.D. ​"Together, we aim to deploy disruptive technology that will enable us to completely reimagine how we identify and pursue therapeutic targets, with the goal of creating new therapies for patients faster than ever before."

Under the agreement terms, Generate:Biomedicines and MD Anderson will share research and development expenses as well as funds generated through commercialization of products that emerge from the collaboration. The organizations also anticipate that MD Anderson will serve as a site and recommend lead investigators for Phase I and II clinical trials of any jointly developed therapeutic product candidates.

About Generative Biology

Generative biology represents a fundamental shift in therapeutic development driven by generative artificial intelligence (AI). This approach creates never-before-seen therapeutic molecules targeted to specific biological processes involved in disease that can be modulated with a wide range of protein modalities—from short peptides to complex antibodies, enzymes, and cytokines. But the promise of generative biology goes beyond existing proteins found in nature and can create novel proteins that are purpose-built to address an existing or emerging therapeutic need. As a result, generative biology promises to leave trial-and-error drug discovery methods behind to usher in a new era of programmable drug generation that’s faster, cheaper, and better tailored to specific conditions.

Orion Group Interim Report

On April 27, 2023 Orion reported its interim report (Press release, Orion, APR 27, 2023, View Source [SID1234632997]).

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Consolidated Financial Results for Year Ended March 31, 2023 (Fiscal 2022)

On April 27, 2023 Daiichi Sankyo reported its Consolidated Financial Results for Year Ended March 31, 2023 (Press release, Daiichi Sankyo, APR 27, 2023, View Source [SID1234632949]).

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First Quarter 2023

On April 27, 2023 Merck & Co reported its first quarter 2023 results (Presentation, Merck & Co, APR 27, 2023, View Source [SID1234632867]).

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