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A Study of TAS0728 in Patients With Solid Tumors With HER2 or HER3 Abnormalities


ABSTRACT: This is a First-in-Human (FIH), 2-part, Phase 1/2, open-label, multicenter study design to evaluate the safety, tolerability, PK, pharmacodynamics, PGx, and efficacy of TAS0728. This study consists of Phase 1 and Phase 2 components in subjects with advanced solid tumors with HER2 or HER3 overexpression, amplification, or mutation who have progressed despite standard therapy or for which no standard therapy exists, particularly urothelial cancer, biliary tract cancer, metastatic breast cancer, non-small cell lung cancer and colorectal cancer.

DISEASE(S): Advanced Solid Tumors With Her3 Abnormalities,Congenital Abnormalities,Breast Cancer Female,Urothelial Cancer Of Renal Pelvis,Advanced Solid Tumors With Her2 Abnormalities,Urothelial Cancer With Her2 Or Her3 Mutationbiliary Tract Cancer With Her2 Or Her3 Mutationbreast Cancer With Her2 Or Her3 Mutationbreast Cancer With Her2 Amplification/overexpression As Per Asco-cap 2013 Guidelinesnon-small Cell Lung Cancer (nsclc) With Her2 Or Her3 Mutationcolorectal Cancer (crc) With Her2 Mutation Or Amplification Other Tumors With Her2 Or Her3 Mutation, Amplification, Or Overexpression (eg, Gastric Or Gastroesophageal Junction (gej), Endometrial),Colorectal Cancer,Bile Duct Cancer,Urothelial Cancer With Her2 Or Her3 Mutationbiliary Tract Cancer With Her2 Or Her3 Mutationbreast Cancer With Her2 Or Her3 Mutationbreast Cancer With Her2 Amplification/overexpression As Per As...,Non-squamous Non-small Cell Lung Cancer,Neoplasms,Solid Tumors

PROVIDER: 2264167 | ecrin-mdr-crc |

REPOSITORIES: ECRIN MDR

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