Mural Oncology Announces Upcoming Presentations at 2024 American Association for Cancer Research (AACR) Annual Meeting

On March 5, 2024 Mural Oncology plc (Nasdaq: MURA), a clinical-stage immuno-oncology company developing novel, investigational engineered cytokine therapies designed to address areas of unmet need for patients with a variety of cancers, reported two upcoming poster presentations at the American Association for Cancer Research (AACR) (Free AACR Whitepaper) annual meeting taking place April 5-10 in San Diego (Press release, Mural Oncology, MAR 5, 2024, View Source [SID1234640758]). The presentations will be the first time Mural will share preclinical data from its IL-18 and IL-12 programs.

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The details are as follows:

Interleukin-18 engineered for resistance to IL-18 binding protein (IL-18BP) and half-life extension to enhance its therapeutic potential
Session: Immune Modulation with Cytokines
Date and Time: Tuesday Apr 9, 2024, 9:00 a.m. – 12:30 p.m. PST
Location: Poster Section 4, Poster 20
Abstract #: 4076
Speaker/Lead Author: Mark Whitmore, Ph.D., Mural Oncology

Generation of tumor targeted self-assembling split IL-12 subunits for the treatment of cancer
Session: Immune Modulation with Cytokines
Date and Time: Tuesday Apr 9, 2024, 9:00 a.m. – 12:30 p.m. PST
Location: Poster Section 4, Poster 10
Abstract #: 4066
Speaker/Lead Author: Joshua Heiber, Ph.D., Mural Oncology

All posters will be made available at View Source following the presentations.

Transgene, NEC, and BostonGene Expand Collaboration for Phase I/II Clinical Trial of Neoantigen Cancer Vaccine TG4050

On March 5, 2024 Transgene (Euronext Paris: TNG), a biotech company that designs and develops virus-based immunotherapies for the treatment of cancer, NEC Corporation (NEC; TSE: 6701), a leader in IT, network and AI technologies and BostonGene Corporation (BostonGene), a leading company in AI-based molecular and immune profiling, reported the expansion of their collaboration for the randomized Phase I/II trial of TG4050, an individualized therapeutic vaccine for patients with head and neck cancers (Press release, NEC, MAR 5, 2024, View Source [SID1234640734]).

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BostonGene is partnering with NEC and Transgene to continue performing tumor molecular profiling and microenvironment analysis and provide high-throughput sequencing services. The partnership with BostonGene will enable fast turnaround of next-generation sequencing (NGS) data, and sophisticated analytics will enable comprehensive profiling of patient immune contexture.

TG4050, a personalized immunotherapy designed to stimulate the immune system of patients to induce a neoantigen specific T-cell response that can recognize and destroy tumor cells, is based on Transgene’s myvac platform and powered by NEC’s AI-driven Neoantigen Prediction System.

"Our collaboration with BostonGene has provided in-depth information on patient phenotypes in the Phase I trial. It has allowed us to understand the baseline status of our patients and how the tumor micro-environment (TME) might evolve following treatment," said Dr. Alessandro Riva, Chairman and CEO of Transgene.

"The combined expertise of Transgene, NEC and BostonGene will continue to provide a streamlined pipeline for the timely delivery of patient-tailored vaccines as well as data to guide the future development of new personalized treatment options, elevating the standard of care for head and neck cancer patients," said Masamitsu Kitase, Corporate SVP and Head of the Healthcare and Life Sciences Division at NEC Corporation.

"We are committed to supporting Transgene and NEC as they advance these clinical trials," said Nathan Fowler, MD, Chief Medical Officer at BostonGene. "Our molecular and immune profiling techniques comprehensively analyze the tumor, microenvironment, and immune system to identify key predictors of response to TG4050, ultimately improving treatment outcomes."

About myvac
myvac is a viral vector (MVA – Modified Vaccinia Ankara) based, individualized immunotherapy platform that has been developed by Transgene to target solid tumors. myvac-derived products are designed to stimulate the patient’s immune system to recognize and destroy tumors using their own cancer specific genetic mutations. Transgene has set up an innovative network that combines bioengineering, digital transformation, established vectorization know-how and unique manufacturing capabilities. Transgene has been awarded "Investment for the Future" funding from Bpifrance for the development of its platform myvac. TG4050 is the first myvac-derived product being evaluated in clinical trials.

About TG4050
TG4050 is an individualized immunotherapy being developed for solid tumors that is based on Transgene’s myvac technology and powered by NEC’s longstanding artificial intelligence (AI) and machine learning (ML) expertise. This virus-based therapeutic vaccine encodes neoantigens (patient-specific mutations) identified and selected by NEC’s Neoantigen Prediction System. The prediction system is based on more than two decades of expertise in AI and has been trained on proprietary data allowing it to accurately prioritize and select the most immunogenic sequences.

TG4050 is designed to stimulate the immune system of patients in order to induce a T-cell response that is able to recognize and destroy tumor cells based on their own neoantigens. This individualized immunotherapy is developed and produced for each patient.

Initial immunological and clinical data from the ongoing Phase I trial in the adjuvant treatment of HPV-negative head and neck cancers were presented at several conferences in 2023 and are very encouraging.

BetaGlue® Secures €10m EIC Accelerator Award

On March 4, 2024 BetaGlue Technologies S.p.A. ("BetaGlue" or the "Company") a clinical stage company developing novel medical device products in the field of loco-regional radiotherapy to treat solid tumour cancers called ‘BAT-90’, reported that it has been successful in its application for a €10m EIC Accelerator award.

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The European Innovation Council (EIC) Accelerator program is the most competitive of its kind in Europe.
For the November 2023 cut-off just 42 of 1,083 (~4%) applicants were successful.
The application process includes a detailed written submission, and then if short-listed, face-to-face cross-examination by a highly experienced jury panel.
The €10m award consists of a €2.5m grant component and a €7.5m equity component. The capital will be used to further advance the clinical development of the BAT-90 platform in multiple solid tumour cancer indications.

"The rigorous EIC Accelerator review process involves a high degree of technical and commercial scrutiny. Our success is testament to the clinical and commercial impact potential of our platform technology, and moreover, to the world-class executive team that have made this tremendous accomplishment" said Dr Colin Story, CEO.

(Press release, BetaGlue Technologies, MAR 4, 2024, View Source [SID1234661235])

Proen Therapeutics Attracts Strategic Investment from Korea Kolmar Holdings

On March 4, 2024 Proen Therapeutics, a company specializing in the development of new anticancer drugs, reported that it has completed a strategic investment from global beauty and bio-healthcare company Korea Kolmar Holdings (Press release, ProEn Therapeutics, MAR 4, 2024, View Source;bmode=view&idx=19525174&t=board [SID1234649258]). Both parties agreed not to disclose the investment amount.

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This investment was conducted in an open innovation program jointly hosted by Korea Kolmar Holdings and the Hongneung Gangseo Special Zone Business Group to support the discovery of promising companies and investment activation by evaluating their technological prowess, marketability, and potential for follow-up collaboration, and Proen Therapeutics was selected as a result.

Proen Therapeutics is a company that has competitiveness in the development of antibody functional parts among antibody-drug conjugate (ADC) new drug development companies that have recently been receiving increasing attention worldwide.

The company’s ‘ArtBodyTM’ technology, a platform technology that develops cancer antigen-specific binding proteins optimized for ADCs, is a technology that can significantly improve toxicity to normal cells and tissues, which is a limitation of existing antibody-based ADCs. It is Proen Therapeutics’ exclusive platform technology that maximizes the selective binding characteristics of cancer cells.

As part of its strategic investment and open innovation cooperation, Korea Kolmar Holdings will continue to pursue joint development projects between its affiliates HK inno.N and Proen Therapeutics. As a top priority, it signed a joint development contract for a CAR-T new drug for the treatment of solid cancer.

Proen Therapeutics CEO Lee Il-han said, "Through this strategic investment and joint research agreement, we expect to discover competitive candidate substances and accelerate R&D through the synergy effects of the technologies owned by both companies."

DB007 enters animal efficacy studies

On March 4, 2024 DotBio reported its lead candidate, DB007, has begun animal efficacy studies (Press release, DotBio, MAR 4, 2024, View Source [SID1234646740]). DB007 is a tri-specific antibody designed to reinvigorate exhausted immune cells to fight cancer more effectively. This study was conducted in the Agency for Science, Technology and Research (A*STAR).

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