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Servier Standardizes Data Across 80+ Countries With Veeva OpenData

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Servier Standardizes Data Across 80+ Countries With Veeva OpenData

Barcelona – September 30, 2026 -- Servier is standardizing customer reference data across more than 80 countries using Veeva OpenData, part of a global push to build an AI-ready data foundation for its commercial and medical teams.

Servier scales AI infrastructure after prior success with Veeva Link Key People

The French pharmaceutical company, governed by a Foundation, is harmonizing customer reference data globally to create a unified semantic layer that connects with Veeva Link. Liam Hanrahan, director of world operations excellence at Servier, said the move goes beyond process improvement, calling it the construction of a global data foundation designed to redefine how the company operates and scale AI across its affiliates.

Insilico Medicine Nominates AI-Designed GIPR Antagonist ISM1354

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Insilico Medicine Nominates AI-Designed GIPR Antagonist ISM1354

Cambridge, Mass. – September 30, 2026 -- Insilico Medicine (HKEX: 3696) has nominated ISM1354, an AI-designed small molecule GIPR antagonist, as a preclinical candidate for obesity, type 2 diabetes and potential cardiovascular applications tied to obesity-associated heart failure.

ISM1354 improves on Insilico's earlier GIPR candidate ISM0676
The company nominated ISM0676, a prior GIPR antagonist, in January, which showed up to 31.3% weight loss in combination with Semaglutide in humanized mouse models. ISM1354 retains comparable weight-loss efficacy while delivering improved pharmacokinetic and safety profiles, addressing tolerability issues that have derailed rival GIPR programs industry-wide.

IDEAYA, Servier Dose First Patient in Phase 3 Uveal Melanoma Trial

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IDEAYA, Servier Dose First Patient in Phase 3 Uveal Melanoma Trial

South San Francisco, Calif. – September 12, 2026 -- IDEAYA Biosciences and Servier have dosed the first patient in OptimUM-11, a global Phase 3 trial testing darovasertib combined with crizotinib as adjuvant therapy for primary uveal melanoma, targeting a disease segment with no approved systemic treatment options.

Trial design pairs oral PKC and cMET inhibitors for high-risk patients post-local therapy

OptimUM-11 will enroll approximately 450 patients who have completed local therapy for primary uveal melanoma and face elevated risk of metastatic recurrence. Patients will be randomized 1:1 to receive darovasertib plus crizotinib for 12 months or to observation, regardless of HLA status. The primary endpoint is relapse-free survival.