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Unfolding The Next Generation Of Allosteric Small Molecule Therapies To Meet Patient Needs
Combining physics-based methods with artificial intelligence, Gain is developing best-in-class small molecules for disorders with high unmet medical need.
Lead Program

Gain’s lead drug candidate GT-02287 is a best-in-class small molecule, for the treatment of GBA-Parkinson’s disease and other neurodegenerative diseases. GT-02287 is currently being evaluated in a Phase I clinical study.

OUR DRUG DISCOVERY PLATFORM MAGELLANâ„¢

By leveraging AI-supported 3D structural biology and supercomputer-powered proprietary physics-based models, Gain’s Magellan™ platform is able to identify novel allosteric binding sites on disease-implicated proteins and exploit their untapped opportunities, by pinpointing pockets that cannot be found or drugged with current technologies.

ALLOSTERIC PROTEIN REGULATION

Our next generation allosteric small molecule therapeutics can modulate a protein to restore or disrupt function, not just through inhibition or activation, but also through stabilization, destabilization and degradation, based on disease pathology.

Corporate Presentation
December 2024
Corporate Presentation