Gilead Sciences has entered a strategic partnership with Terray Therapeutics for the discovery and development of small-molecule therapies across several targets.

The partnership leverages Terray’s AI-driven platform, tNova, designed to enhance drug discovery via high-throughput chemical experimentation and computational analysis.

Terray will leverage its platform to identify and develop compounds for targets chosen by Gilead.

If Gilead opts to license these compounds exclusively, it will assume responsibility for their subsequent development and commercialisation.

Terray is set to obtain an upfront payment and may also earn milestone payments upon reaching preclinical, clinical and sales targets. It will gain tiered royalties on net sales of any products that would be commercialised by Gilead as a result of the partnership.

Terray Therapeutics CEO Jacob Berlin stated: “We’re very excited to put tNova’s unique blend of experimentation and computation to work alongside the deep expertise of our collaborators at Gilead to find transformational small molecule therapeutics that bring relief to patients in need.”

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The deal will impact Gilead’s financials, with an expected reduction in both GAAP [generally accepted accounting principles] and non-GAAP 2024 EPS [earnings per share] by $0.01. The company includes acquired in-process research and development expenses in its non-GAAP financial measures.

Gilead Sciences Research executive vice-president Flavius Martin stated: “Next-generation, AI-driven platforms using custom-generated large, relevant data sets will serve as important tools in our efforts to shape the future of drug discovery in our ongoing pursuit of innovative treatments across our therapeutic areas of focus.

“We are excited to collaborate with Terray and explore how their integrated discovery platform will complement our own internal research capabilities and expertise.”

In a separate announcement, Gilead’s Trodelvy received breakthrough therapy designation from the US Food and Drug Administration (FDA) for treating adults with extensive-stage small cell lung cancer post-platinum-based chemotherapy. This designation stems from the Phase II TROPiCS-03 trial ES-SCLC cohort outcomes.

In September 2024, Gilead announced a strategic partnership with Genesis Therapeutics, focusing on AI to discover and develop new small molecule therapies.