MaaT Pharma Provides Third Quarter 2024 Business and Financial Results and Announces Management Changes

On November 5, 2024 MaaT Pharma (EURONEXT: MAAT – the "Company"), a clinical-stage biotechnology company and a leader in the development of Microbiome Ecosystem TherapiesTM (MET) dedicated to enhancing survival for patients with cancer through immune modulation, reported a business update and provided its cash position and revenue as of September 30, 2024 (Press release, MaaT Pharma, NOV 5, 2024, View Source [SID1234647689]).

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Pipeline highlights

MaaT013

In hemato-oncology:
In September 2024, MaaT Pharma announced that MaaT013 batches were ready for distribution for clinical supply in the US and that MaaT Pharma advanced the readiness phase for the initiation of clinical activities.
In October 2024, MaaT Pharma announced the completion of patient recruitment for ARES, its European Phase 3 clinical trial designed to evaluate the efficacy and safety of its lead asset MaaT013 in the treatment of steroid refractory and ruxolitinib refractory or intolerant acute Graft-versus-Host Disease (aGvHD) (NCT04769895).
MaaT033

In hemato-oncology:
In July 2024, the Company announced that the DSMB completed its first safety assessment of the Phase 2b trial PHOEBUS (NCT05762211) aiming at assessing MaaT033 impact in improving overall survival in patients receiving hematopoietic stem cell transplantation, and recommended continuation of the trial without modification. The trial is a European, multi-center, randomized, double-blind study, testing MaaT033, an oral freeze-dried formulation against placebo, set to be conducted in up to 56 clinical investigation sites and expected to enroll 387 patients.
Cash position1

As of September 30, 2024, total cash and cash equivalents were EUR 27 million, as compared to EUR 31.2 million as of June 30, 2024, and EUR 24.3 million as of December 31, 2023. The net decrease in cash position of EUR 4.2 million during the third quarter 2024 reflects continued investments in R&D activities across the pipeline, offset in part by the payment of a repayable advance of EUR 3.2 million in public funding the development of MaaT033 and the balance of the 2023 R&D tax credit of EUR 1.0 million.
The Company believes it has sufficient cash to cover its current operating needs and development programs into the second quarter of 2025.
Revenues in Q3 20241

MaaT Pharma reported revenues from its Early Access Program of EUR 0.6 million for the quarter ended September 30, 2024, an increase of EUR 0.2 million over the third quarter of 2023. Total revenues for the first nine months of 2024 amounted to EUR 2.3 million compared with EUR 1.8 million for the same period of 20231. This trend is a direct reflection of the continued demand from the medical community for MaaT Pharma’s drug candidate MaaT013.
Management Changes

Eric Soyer was appointed Chief Financial Officer of MaaT Pharma as of November 2024. As CFO, Eric will supervise all corporate functions, investor relations, legal affairs and human resources. Eric is a senior financial executive with extensive experience in the biotech industry with companies listed on Euronext Paris and on the U.S. Nasdaq market. Prior to joining MaaT Pharma, Eric successfully conducted as CFO & COO of Erytech Pharma, a French late-stage drug development company, its Nasdaq IPO and subsequent financial rounds amounting to over EUR 300 million and supervised the scale-up of the company’s operations from a single site based in France to a multi-site company of 240 employees in US and Europe and most recently its strategic merger. Throughout his 30-year career, Eric has developed a solid international experience across a variety of operational settings and will now leverage this experience to assist MaaT Pharma in its next stage of development.
Eric Soyer, CFO of MaaT Pharma stated: "I am thrilled to join the team of MaaT Pharma at this transformational moment for the Company. MaaT Pharma has developed a robust foundation and is now one of the oncology worldwide leaders for microbiome-based therapeutic innovations, as evidenced by the recent announcement of the completion of patient enrollment in its Phase 3 ARES European trial in aGvHD – a significant milestone in the goal of bringing life-saving therapeutic options for patients within this severe indication. I look forward to contributing to MaaT Pharma’s continued success and to fully realize the potential of its therapeutic platform globally."
After 8 years as CFO, Siân Crouzet will become Chief of Staff to fully support a smooth transition of functions to Eric over the coming months. In her tenure, Siân has successfully structured the financial and administrative functions of the Company, building a competent team across the various functions overseen and with strict discipline to support the corporate goals and progressive growth in a highly challenging economic context. Siân was instrumental in the numerous financing operations accomplished since 2016, totaling more than EUR 115 million, including the Company’s successful IPO on Euronext Paris in November 2021.
Siân Crouzet, CoStaff of MaaT Pharma stated: "I am proud of the Company we have built and developed as a team and the numerous accomplishments, not least the recent completion of enrolment of our Phase 3 clinical trial of MaaT013. It has been a real pleasure and honor to serve as CFO over the last 8 years. At this juncture, it is the right time from a professional and personal perspective for me to hand over the reins to take MaaT Pharma to the next stage of its development."
Hervé Affagard, CEO and co-founder of MaaT Pharma added: "I am delighted to welcome Eric Soyer as our new Chief Financial Officer. His extensive experience and strategic financial acumen will be invaluable as we continue to advance our mission to improve survival in patients with few therapeutic options. MaaT Pharma is at a turning point with the preparation of the filing of MaaT013, in Europe, for severe GvHD patients together with our goal to expand in the US. I am confident that Eric will bring the necessary skills to the team to navigate the next chapter of our growth. I also want to take a moment to extend my heartfelt thanks to Siân Crouzet for her invaluable contributions over the past 8 years. She has been instrumental in strengthening our financial foundation and steering us through important phases of development."
Upcoming investor and medical conferences participation

November 6-8, 2024 – 39th SITC (Free SITC Whitepaper) annual meeting in Houston, USA
November 20-22, 2024 – SFGM-TC annual meeting in Toulouse, France
November 25-27, 2024 – Deutsches Eigenkapitalforum annual meeting​​ in Frankfurt, Germany
November 26, 2024 – Investir Day event in Paris, France.
December 5, 2024 – CF&B Midcap Events in Geneva, Switzerland
December 7-10, 2024 – 66th ASH (Free ASH Whitepaper) annual meeting in San Diego, USA, followed by a webinar on the updated dataset from the EAP of MaaT013 in aGvHD.

PharmaMar receives a $10 million payment from Janssen as a commercial milestone

On November 5, 2024 PharmaMar Group (MSE: PHM) has received a $10 million payment from Janssen Products LP (Janssen), a subsidiary of Johnson & Johnson, upon reaching a commercial milestone established in the licensing agreement for Yondelis (trabectedin) in the United States (Press release, PharmaMar, NOV 5, 2024, View Source [SID1234647674]).

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In August 2019, PharmaMar signed a new licensing agreement with Johnson & Johnson that replaced the 2001 agreement under which Johnson & Johnson reserved the right to exclusively sell and distribute trabectedin in the United States.

Currently, trabectedin is approved in more than 70 countries for the treatment of soft tissue sarcoma and also in some of these countries for ovarian cancer.

Transgene and ProBioGen Join Forces
to Advance Individualized Cancer Vaccine Development

On November 5, 2024 Transgene (Euronext Paris: TNG), a biotech company that designs and develops virus-based immunotherapies for the treatment of cancer, and ProBioGen, a leading CDMO in biologics, vaccines and viral vectors, reported that the companies have entered into a license agreement for ProBioGen’s AGE1.CR.pIX suspension cell line (Press release, Transgene, NOV 5, 2024, View Source [SID1234647673]). This partnership aims to add value by combining ProBioGen’s specific production technology with the manufacturing capabilities of Transgene’s individualized cancer vaccine program and its myvac platform.

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ProBioGen’s AGE1.CR.pIX suspension cell line showcases innovation and reliability in bioprocessing with a proven track record and is currently in use for multiple late-stage clinical trials. Renowned for its high yield and scalability, this platform enables efficient industrial manufacturing processes, translating into cost-effectiveness and increased productivity in manufacturing. Additionally, the AGE1.CR.pIX cell line offers robust growth and excellent genetic stability to ensure consistent and reliable production.

"We are delighted to embark on this collaborative journey with ProBioGen," said Dr. Alessandro Riva, CEO of Transgene. "The AGE1.CR.pIX suspension cell line represents a significant addition to further expand the manufacturing processes for our individualized cancer vaccines while we work towards providing patients with tailored patient-specific therapies against cancer on a larger scale."

The partnership between Transgene and ProBioGen underscores a shared commitment to advancing the field of individualized medicine and to support manufacturing scalability and optimization.

"We are thrilled to partner with Transgene in advancing the frontier of personalized cancer vaccines," said Dr. Volker Sandig, CSO of ProBioGen. "Our collaboration holds immense potential to impact the personalized vaccine space and to offer new treatments and hope to cancer patients."

Ring Therapeutics Announces New Strategic Partnerships with A*STAR and SERI to Establish Gene Therapy R&D Efforts in Singapore, a Growing Global Biotech Hub

On November 4, 2024 Ring Therapeutics, a life sciences company founded by Flagship Pioneering to revolutionize gene therapy with its commensal virome platform, reported new strategic partnerships with the Agency for Science, Technology, and Research (A*STAR), Singapore’s lead public sector R&D agency; and the Singapore Eye Research Institute (SERI) to advance innovative R&D efforts and support the continued development of the biomedical science ecosystem in the region (Press release, Ring Therapeutics, NOV 4, 2024, View Source [SID1234656557]).

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"The strategic benefits for the company are profound and span the entirety of the platform, from early discovery work where we plan to characterize novel anellovirus genomes to enable ophthalmology and oncology applications, to indication portfolio expansion via the testing of novel payloads across multiple therapeutic areas, to enhancing process performance for our next-generation manufacturing platform," said Tuyen Ong, MD, MBA, Chief Executive Officer at Ring Therapeutics and CEO-Partner at Flagship Pioneering. "Through engaging a global ecosystem of R&D experts, these partnerships will further expand the potential of our Anellogy platform and aim to accelerate the clinical translation of our AnelloVector therapeutics."

The A*STAR and SERI partnership will accelerate the creation of new potential treatments for eye diseases (ophthalmology) and cancer (oncology), while also improving the methods and technologies needed to produce these treatments. The collaboration will bring together synergistic expertise in scale-up manufacturing and capabilities for continued advancements of scientific breakthroughs and technological development in the region.

Professor Tan Sze Wee, Assistant Chief Executive, Biomedical Research Council, A*STAR, added, "We are excited to partner with Ring Therapeutics, whose pioneering platform technology complements our mission to advance innovative medicines. By bringing together our technologies and premier research capabilities, this collaboration holds great promise for translating groundbreaking discoveries into impactful therapeutic solutions for patients. We believe this strategic fit will foster continued scientific collaboration and inspire advanced R&D development within the Singapore biotech ecosystem, ultimately bringing impact and benefiting those in need."

Professor Jodhbir Mehta, Executive Director, SERI, added, "Gene therapy presents an exciting opportunity to treat ophthalmic diseases that previously had no effective treatments. This partnership will allow SERI to further develop Ring’s novel class of viral vector that has higher tropism and is potentially redosable. We look forward to making significant strides in developing groundbreaking therapies that will reduce vision impairment."

Caszyme and Integra Therapeutics sign licensing agreement for novel CRISPR Cas12l nucleases

On November 4, 2024 Caszyme, a pioneer in the development and application of CRISPR gene editing technology, and Integra Therapeutics, a company leading the way in creating advanced therapies based on next-generation gene-writing tools, reported a licensing agreement for the use of Caszyme’s novel Cas12l nucleases to develop safer and more efficient gene and cell therapies (Press release, Integra Therapeutics, NOV 4, 2024, View Source [SID1234654539]).

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The agreement was unveiled at this year’s BIO Europe, which is the largest partnering event for the biomedical industry in Europe, taking place this week in Stockholm. Over 2,800 companies attended from 60 countries, with more than 5,000 biopharma professionals in attendance.

Under the agreement, Integra Therapeutics will incorporate the genome editor Cas12l into its FiCAT 2.0 (Find and Cut-And-Transfer) gene-writing platform, following successful in vivo and ex vivo studies, which yielded highly positive results in terms of safety and functionality in human cells. Caszyme will receive milestone payments up to 40 million. euros in addition to royalties on sales.

Cas12l is a unique CRISPR nuclease family with an effector size of approximately 850 amino acids that stands out for its small size and versatility. As the demand for efficient and safe gene-editing tools in therapeutic contexts continues to grow, these small nucleases represent a promising solution, combining efficacy with the practical advantages of reduced size. Caszyme-developed Cas12l shows great activity in human cells across multiple targets.

Compared to other nucleases, Caszyme’s Cas12l offers additional delivery possibilities, especially when combined with other effector domains. Moreover, smaller nucleases from non-pathogenic bacteria may be less immunogenic compared to their larger counterparts, further highlighting their therapeutic potential. The nucleases discovered by Caszyme exhibit different characteristics from Cas9 nucleases, which formed the foundation of the find module in FiCAT 1.0, expanding their potential applications in advanced therapies.

"Caszyme’s goal is to enable therapeutic companies to develop novel, efficient and affordable gene editing modalities. This collaboration with Integra Therapeutics is a perfect alignment between two highly innovative European companies, and when successful, will help bring advanced gene editing based therapies to the market." said Dr Monika Paulė, CEO and Co-Founder of Caszyme.

Adding, Dr Giedrius Gasiunas, CSO and Co-Founder of Caszyme, said "the partnership will further Caszyme’s core scientific aims – which are to develop novel, safer and smaller Cas12l nucleases that are more compatible with diverse delivery technologies, such as AAVs, mRNA and LNPs."

Dr Avencia Sánchez-Mejías, CEO and Co-Founder of Integra Therapeutics, added, "This agreement with Caszyme reaffirms our commitment with the excellence in technology development to delivery therapeutic solutions for patients with our gene-writing technology in the preclinical regulatory phase and highlights the success of the transnational project funded by the European Commission, which we launched in 2022 through Eurostars, in support of Europe’s most innovative SMEs."

"The integration of Caszyme nucleases into our FiCAT 2.0 platform strengthens Integra Therapeutics’ mission to develop the highest-quality gene and cell therapy products for the treatment of a wide range of genetic and oncological diseases. FiCAT 2.0 will set itself apart in the market by offering enhanced precision and efficiency," explained Dr Marc Güell, CSO and Co-Founder of Integra Therapeutics.