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Contemporary design of small-molecule kinase modulators: orthosteric, allosteric and induced-proximity strategies

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Targeting PI3Kδ suppresses pancreatic cancer by dual disruption of fibrosis and immune evasion

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Roginolisib stabilizes inactive PI3Kδ to deliver specific target blockade with reduced immune toxicity

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A renaissance in targeting the PI3K/AKT/mTOR pathway

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IOA-244, a novel p110δ PI3K inhibitor, blocks breast tumour progression on either mono- or combined-therapy

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The PULMO-01 phase I/IIa Study of Roginolisib in combination with dostarlimab, with or without docetaxel, in patients with advanced non-squamous NSCLC who have progressed on standard of care therapy

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The PI3Kδ inhibitor roginolisib (IOA-244) preserves T-cell function and activity

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iOnctura CEO to present at the 2026 J.P. Morgan Healthcare Conference

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Drug Discovery World – Autotaxin inhibition: unlocking new frontiers in cancers and beyond

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Novel PI3kδ inhibitor roginolisib synergizes with venetoclax in hematologic malignancies

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The selective PI3Kδ inhibitor roginolisib synergizes with ruxolitinib against progenitor cells from naïve and JAKi-refractory/resistant patients with myelofibrosis

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Roginolisib (IOA-244), an orally bioavailable, selective PI3Kδ inhibitor, in combination with venetoclax and rituximab in patients with relapsed chronic lymphocytic leukemia (CLL)

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