Evozyne Announces Multi-Target Research Collaboration and License Agreement with Takeda to Develop Next-Generation Gene Therapies

On April 5, 2022 Evozyne, Inc., an adaptive biology company pioneering evolution-based design of proteins, founded by Paragon Biosciences, reported that it has entered into a strategic research collaboration and license agreement with Takeda to research and develop proteins that could be incorporated into next-generation gene therapies for up to four rare disease targets (Press release, Takeda, APR 5, 2022, View Source [SID1234611444]). This new agreement builds upon an earlier, separate agreement with Takeda and demonstrates the potential of Evozyne’s protein engineering platform.

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In partnership with Takeda, Evozyne will create novel protein sequences for advancement as gene therapies. At completion and review of certain research deliverables, Takeda has the option to obtain an exclusive license to develop and commercialize the novel protein sequences as part of its gene therapy program. Under the terms of the agreement, Evozyne will receive double-digit million dollars in upfront and research funding payments. The company is also eligible to receive future developmental, regulatory and commercial milestone payments of up to $400 million if all milestones are achieved in target indications over the course of the partnership plus tiered royalties on net sales of any commercial product resulting from the collaboration.

Under the agreement, Evozyne will receive double-digit million dollars in upfront and research funding payments.

"Our continued work with Takeda affirms Evozyne’s unique capability to provide advanced, targeted novel proteins that have remarkable potential in numerous applications," said Evozyne Co-founder and CEO Jeff Aronin. "Through these types of innovative collaborations, Evozyne plays a critical role in accelerating the development of gene therapies to potentially help people living with serious medical conditions."

"Producing highly differentiated transgenes is critical to advancing the next generation of gene therapies," said Madhu Natarajan, Head of the Rare Diseases Drug Discovery Unit at Takeda. "By expanding our collaboration with Evozyne, we have the opportunity to leverage their novel protein engineering platform across new disease targets with the hope of one day delivering functional cures to patients living with rare genetic diseases."

Evozyne’s platform harnesses AI and machine learning technologies with the principles of evolution to uncover nature’s rules. The company integrates its closed-loop learning, high throughput gene synthesis, and automated assays to mimic millions of years of natural evolution in the laboratory. This approach offers a new way to identify novel proteins and improve existing proteins to overcome barriers in disease treatment. By bringing together Takeda’s expertise in the rare disease space with Evozyne’s strength in protein engineering, this collaboration looks to bring meaningful treatments to patients suffering from serious and life-threatening genetic diseases.

"Takeda is helping us make a meaningful difference to the considerable challenges to be solved in rare genetic diseases," said Evozyne Co-founder and Chief Scientific Officer Rama Ranganathan, M.D., Ph.D. "This collaboration allows the continued development of next-generation gene therapies that have the potential to make a positive impact on patients suffering from serious and life-threatening genetic diseases."

AACR-2022 NI-3201 CD28 bispecific antibody platform

On April 5, 2022 The American Association for Cancer Research (AACR) (Free AACR Whitepaper) reported that it will host its Annual Meeting April 8-13, 2022 (Presentation, Light Chain Bioscience, APR 5, 2022, View Source [SID1234611443]). Light Chain Bioscience is very pleased to have Sara Majocchi attend in-person.

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Sara will be presenting a poster (#2884) describing Light Chain Bioscience’s CD28-bispecific antibody platform.

"Optimized CD28 bispecific antibodies for targeted activation of T cells within the tumor microenvironment" will be exposed and presented on April 12 between 9:00 a.m -12:30 p.m.

↠ Read poster – Poster section 37: Will be available on website from April 9th.

Ernest N. Morial Convention Center New Orleans, Louisiana

900 Convention Center Blvd, New Orleans, LA 70130, United States

Evotec SE to announce results for fiscal year 2021 on 12 April 2022

On April 5, 2022 Evotec SE (Frankfurt Stock Exchange: EVT, MDAX/TecDAX, ISIN: DE0005664809; NASDAQ: EVO) reported that it will announce its financial results for 2021 on Tuesday, 12 April 2022 (Press release, Evotec, APR 5, 2022, View Source [SID1234611442]).

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The Company is going to hold a conference call to discuss the results as well as to provide an update on its performance. The conference call will be held in English.

A simultaneous slide presentation for participants dialling in via phone is available at View Source

Webcast details

To join the audio webcast and to access the presentation slides you will find a link on our homepage shortly before the event.

The on-demand version of the webcast will be available on our website: View Source

Redx Announces Collaboration with the Garvan Institute of Medical Research

On April 5, 2022 Redx (AIM: REDX), the clinical-stage biotechnology company focused on discovering and developing novel, small molecule, highly targeted therapeutics for the treatment of cancer and fibrotic disease, reported a collaboration with the Garvan Institute of Medical Research ("the Garvan"), a premier Australian medical research institute, which expands on preclinical work already underway (Press release, Redx Pharma, APR 5, 2022, View Source [SID1234611439]).

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The collaboration aims to better understand treatments that could lead to increased patient survival in currently very poorly treated highly fibrotic cancers, such as pancreatic cancer. Through this collaboration, Redx and the Garvan will develop an enhanced understanding of cancerassociated fibrosis through detailed scientific studies utilising patient-derived tumour tissue grown in mice, which is thereby able to mimic human disease as closely as possible. The research will bring together the Garvan’s research capabilities and leading preclinical cancer models with Redx’s proprietary molecules in development for novel targets potentially implicated in cancer-associated fibrosis, such as Porcupine, ROCK2 and Discoidin Domain Receptors (DDR).

The Garvan is globally renowned for its interest in pancreatic cancer and is currently leading the MoST-P clinical trial programme in conjunction with the University of New South Wales (UNSW) Sydney. The programme provides cancer patients with access to targeted therapies matched to the genomic and/or the fibrotic signature of their tumour or tumour environment. RXC004, a Porcupine inhibitor and Redx’s lead oncology product candidate, is being tested against RNF43 mutant pancreatic cancer and preclinical work is ongoing to determine if the patient population may be expanded beyond RNF43 loss of function patients to include a wider fibrotic signature in pancreatic cancer.

Initial data on proprietary Redx molecules in patient-derived preclinical cancer models from the collaboration are expected to be presented by Professor Marina Pajic, Strategic Program Lead for Precision Medicine for Cancer at the Garvan,at the Extracellular Matrix (ECM) Congress, which will take place in Copenhagen, Denmark on 23-25 June 2022. Further data on patient-derived pancreatic cancer models, expected to be published later in 2022, will enhance insight into Wnt-ligand driven tumours, the target patient group for RXC004, which is currently in Phase 2 development for the treatment of genetically selected pancreatic cancer, genetically selected metastatic colorectal cancer and unselected biliary cancer.

Professor Marina Pajic, Strategic Program Lead for Precision Medicine for Cancer at the Garvan Institute, commented: "We are very pleased to be expanding our partnership with Redx and to be benefitting from its medicinal chemistry expertise to work on a range of molecules under development for these novel targets to discover new therapeutic options for patients with fibrotic cancers, a core area of our research focus."

Dr Caroline Phillips, Head of Oncology at Redx, added: "We are thrilled to be combining the Garvan’s world-leading research in our key areas of focus, fibrotic cancers and cancer associated fibrosis, to explore the potential of Redx’s molecules and novel targets in this leading collaboration. With our focus on fibrosis and oncology and our world-class medicinal chemistry, we are able to contribute a range of molecules from Redx’s differentiated pipeline to further research and develop new targeted therapies for these hard-to-treat conditions."

Lupin Enters into Licensing Agreement with Alvion to market Cardiometabolic Drugs in the Southeast Asia region

On April 5, 2022 Global pharma major, Lupin Limited (Lupin) reported that they have entered into a licensing agreement with Alvion Pharmaceuticals P.C. (Alvion) to commercialize medicines for Cardiometabolic diseases in the Southeast Asia region (Press release, Lupin, APR 5, 2022, View Source [SID1234611438]).

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Lupin is committed to providing new affordable treatment options to healthcare providers and patients. By commercializing cardiometabolic drugs in the Southeast Asian region, Lupin will play a significant role in improving the quality of healthcare and access to medicines.

Commenting on the announcement, Gabriel Georgy, Regional Head Southeast Asia, Lupin said "Forming a long-term collaboration with Alvion to launch a range of therapies will allow Lupin to expand its footprint across Southeast Asia with quality cost effective alternatives for patients and the healthcare system. Both companies have a solid track record of developing and launching products and this agreement will further cement Lupin as a formidable pharmaceutical company in the region. We look forward to expanding our partnership with Alvion over the coming years."

John Bouros, CEO, Alvion said, "Alvion is delighted to partner with Lupin for its important proprietaries and looks forward to launching the products in the Southeast Asia region. Being a leader in value-added medicines, Alvion shall support Lupin’s activities aiming to position both companies at the forefront for both molecules."