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Pfizer, Triana Launch Up-to-$1.5B+ Molecular Glue Collaboration

Pfizer will apply Triana Biomedicines’ target-first and proximity-first discovery platform to discover molecular glue degraders for unspecified “multiple” targets in oncology and several other disease areas, through a collaboration that could generate more tha

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Pfizer will apply Triana Biomedicines’ target-first and proximity-first discovery platform to discover molecular glue degraders for unspecified “multiple” targets in oncology and several other disease areas, through a collaboration that could generate more than $1.5 billion for the Lexington, MA, biotech.

Privately held Triana focuses on building a molecular glue pipeline developed through its platform, which is designed to identify small molecules that induce protein:protein interactions between disease targets and a component of the cell’s ubiquitin-proteasome system (UPS), thus altering the fate or function of the disease target protein.

Triana applies its protein:protein pairing engine to identify E3 ligases that are potential matches, then launches a comprehensive glue discovery campaign covering diverse chemical spaces to identify new molecular glues.

The resulting molecular glue degraders eliminate disease-causing proteins by promoting their interaction with the cell’s UPS—namely enhancing binding between a disease-causing protein and an E3 ligase enzyme. According to Triana, the small molecules can effectively promote the formation of a complex between two proteins even with low binding affinity of the molecular glue to either protein partner.

Triana says it applies genomic, functional, and translational data to prioritize disease targets and candidate E3 ligases for molecular glue discovery, creating a short list from the universe of more than 600 E3 ligases. The company’s technologies are designed to identify preferred E3 ligases for a specific disease target, then discover small molecules that directly promote the interaction of the disease target:E3 ligase pair.

Under their strategic collaboration and licensing agreement, Pfizer has agreed to pay Triana $49 million upfront and potentially more than $1.5 billion in payments tied to achieving milestones, plus tiered royalties.

“This collaboration with Triana Biomedicines on molecular glue discovery reflects our commitment to exploring cutting-edge technologies to drive the next wave of potential breakthroughs,” Jeff Settleman, PhD, CSO of Pfizer Oncology.

Growing interest

Pfizer is the latest biopharma giant over the past couple of years to launch a collaboration focused on molecular glues, reflecting a growing interest in the space.

“It has become clear lately that molecular glue type binding can be considered as a new modality option, specifically for otherwise poorly druggable protein targets,” Angela Zhou, PhD, manager of scientific analysis and insights with CAS, a Division of the American Chemical Society, and colleagues concluded in a 2023 paper reviewing developments in molecular glue development.

Takeda Pharma in May inked an up-to-$1.2 billion, plus royalties, partnership with Degron Therapeutics to develop molecular glue-based therapies for unspecified “multiple” indications in glue candidates in oncology, neuroscience, and inflammation, using Degron’s GlueXplorer® platform. Candidates discovered through Degron’s platform would be shifted to Takeda for further development and commercialization.

Additional targets could be added if the companies exercise their option to expand their collaboration. Takeda also agreed at the time to make an equity investment of an unspecified amount in Degron, which will retain full ownership of its pipeline programs. Degron is based in San Diego and Shanghai, China.

Novo Nordisk launched an up-to-$1.46 billion partnership in February with San Diego-based Neomorph to discover, develop, and commercialize molecular glue degraders for unspecified targets in cardiometabolic and rare diseases, tapping into Novo Nordisk’s expertise in both therapeutic areas.

“This collaboration will enable the expansion of our platform into new therapeutic areas, complementing our ongoing efforts in oncology,” Phil Chamberlain, DPhil, co-founder, president, and CEO of Neomorph, stated at the time.

And in September 2023, Genentech, a Member of the Roche Group, committed $47 million upfront, and potentially up-to-$2 billion-plus in milestone payments toward developing small molecule molecular glue therapies for “major disease areas” that include oncology and neurodegeneration, using Orionis’s Allo-Glue™ platform. Orionis agreed to oversee the discovery and optimization of molecular glues for Genentech’s designated targets, while Genentech is taking responsibility for later-stage preclinical, clinical development, regulatory filing, and commercialization.

Bristol Myers Squibb and Merck & Co. have also initiated molecular glue alliances with smaller partners.

“This collaboration agreement signifies an important milestone in the evolution of Triana, as the company advances toward delivering on its product-focused strategy,” added Patrick Trojer, PhD, Triana’s president and CEO.

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Related questions

01How stable is the antibody?

A crucial question often addressed during preclinical development focuses on the in vivo stability of therapeutic antibodies. Increasing the half-life of a therapeutic antibody has several benefits ranging from higher treatment efficacy to increased advantages for the patients who will have a fewer number of therapy sessions and a reduced cost. Given these compelling benefits, following the identification of therapeutic antibodies with the desired specificity, developers usually subject them to a refinement step to increase their stability. This process is often hindered by the lack of reliable experimental tools to predict the half-life of antibodies in patients. The major hurdle of using mouse models to predict antibody stability in the serum lies in the way immunoglobulin proteins are processed by the organism. In mammals, most proteins circulating in the serum undergo constant uptake by endothelial cells and are routed through the endosomes to the lysosomal compartment for degradation. In the endosomes, immunoglobulin G (IgG) proteins are recognized and bound by a transmembrane protein, called the neonatal Fc receptor (FcRn), which mediates their recycling to the plasma membrane and subsequent release back into the serum. As a result, the half-life of IgGs are significantly extended by this mechanism. Since most therapeutic antibodies belong to the IgG class, this recycling system is very relevant for their relative stability in the body. Remarkably, the relative affinity between IgGs and FcRn is extremely disparate between different species, with the mouse receptor showing a much higher affinity than its human counterpart.

Source: www.genengnews.com ↗
02Undruggable or unscreenable?

Another obstacle to discovering new PPI inhibitors is the lack of libraries designed to hunt for them, points out Philippe Roche, PhD, senior scientist at the Integrative Structural and Chemical Biology team at the Cancer Research Center of Marseilles, France. “If you screen PPIs using libraries that were designed for kinases or GPCRs, that’s why you don’t get a lot of good results,” he says. To that end, his group began assembling a library focused on orthosteric inhibitors of PPIs. The result was 2P2Idb, a hand-curated, structural database cataloguing orthosteric inhibitors of PPIs for which the interface had been 3D characterized. From analyzing these known PPI inhibitors, and what structures they had in common, Roche and his colleagues developed a model to predict whether compounds would likely inhibit PPIs. Using this method, 2P2Idb creates an enriched screening library that dramatically increases the hit rate compared to standard libraries. Having proven their success with a small library of 1600 compounds, they are in the process of expanding the library to 10,000 compounds. Once that’s published, “the idea is to make this library available to labs around the world,” Roche says. “We will provide the library free of charge for people to be able to screen PPI targets.”

Source: www.genengnews.com ↗
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Peptide Therapy Guide Editorial Team

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