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A pipeline of first-in-class therapeutics for intractable targets

We’re advancing multiple small molecule candidates with novel condensate modulating mechanisms for targets that have long proved hard to drug with traditional approaches, like beta-catenin, MYC, and TDP43. Our pipeline of small molecule c-mods have the potential to transform treatment in high unmet need diseases like cancer and ALS.

Our lead beta-catenin program is currently in Phase 1 development for gastric cancer, with fast-track and orphan drug designations. Our TDP43 and MYC programs are in IND-enabling studies, while partnerships with Bayer, Novo Nordisk, and the Gates Foundation are in pre-clinical discovery for a range of diseases.

Leveraging condensates to address previously intractable targets

Explore our platform and how we are unlocking previously hard-to-target drivers of disease.
Condensates organize key molecules into specialized compartments that regulate essential cellular processes like transcription, signaling, and stress response. Many diseases are caused by abnormal condensate behavior that disrupts these functions. Because condensate properties differ between healthy and diseased states, they create an opportunity to selectively modulate disease-driving biology while leaving normal function in-tact.

Our platform is designed to identify and selectively target these pathological condensates using novel mechanisms that restore healthy function. Because condensates are enriched in disordered proteins that are hard to target with traditional approaches, this includes targets that were previously intractable with small molecules like beta-catenin, MYC, and TDP-43.

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