Japanese drugmaker Takeda will present data on both its investigational and marketed assets at the upcoming annual meeting of the American Society of Clinical Oncology.
Results from a Phase I/II first-in-human, open-label, multicenter study of TAK-788 will be presented orally. The ongoing study is investigating the antitumor activity and safety of TAK-788 in patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) whose tumors harbor EGFR exon 20 insertion mutations.
Takeda also will present three posters on the treatment of patients with ALK+ NSCLC with Alunbrig (brigatinib), and there will be further presentations in blood cancers, including from the Phase III PhALLCON trial – an ongoing efficacy study of Iclusig (ponatinib) in combination with reduced-intensity chemotherapy in newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia.
Additional data from the ECHELON-1 and ECHELON-2 trials evaluating Adcetris (brentuximab vedotin) as a frontline treatment option in newly-diagnosed Stage III and IV Hodgkin lymphoma and in CD30+ peripheral T-cell lymphoma, respectively, will also be shared in partnership with Seattle Genetics.
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