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A bold new era in global cancer drug discovery

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All articles

iOnctura announces FDA clearance of IND application for roginolisib, a first-in-class allosteric modulator of PI3Kδ

New research highlights potential of iOnctura strategy combining autotaxin and TGF-β inhibitors in cancer

Autotaxin secretion is a stromal mechanism of adaptive resistance to TGFβ inhibition in pancreatic ductal adenocarcinoma

Drug Discovery World — Meet the researcher: Giusy Di Conza

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

pharmaphorum — Realising the potential of autotaxin inhibition in cancer

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

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

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

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

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

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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