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Non-clinical toxicology evaluation of the novel non-ATP competitive oral PI3 kinase delta inhibitor roginolisib

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pharmaphorum — Realising the potential of autotaxin inhibition in cancer

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Autotaxin inhibitor IOA-289 reduces gastrointestinal cancer progression in preclinical models

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Autotaxin inhibition with IOA-289 decreases breast tumor growth in mice whereas knockout of autotaxin in adipocytes does not

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TLR-X (IOA-359) attenuates steatosis and fibrosis in a preclinical NASH model

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IOA-289, an orally available type IV autotaxin inhibitor, ameliorates steatosis and fibrosis in a progressive preclinical murine NASH model

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Patient derived tumor cells identify mechanistically rational combinations for the PI3Kδ inhibitor roginolisib in solid and hematologic malignancies

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Highly selective allosteric modulator of the phosphoinositide 3-kinase data (PI3Kδ) roginolisib (IOA-244) in a dose escalation study of patients with refractory/relapsed follicular lymphoma (FL)

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First-in-human (FIH) phase I dose escalation study (part A) of the first oral allosteric modulator of phosphoinositide 3-kinase inhibitor delta (PI3Kδ) roginolisib in patients with advanced cancer and dose confirmation in uveal melanoma (part B)

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Characterization and translational development of IOA-289, a novel autotaxin inhibitor for the treatment of solid tumors

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iOnctura to present research at leading scientific conferences in June 2023

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Peer-reviewed translational research paves the way for first-in-class autotaxin inhibitor IOA-289 in cancer

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