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Clinical Trials associated with DAT-1604 / Not yet recruitingPhase 1 Phase 1 Study to Evaluate the Safety, Tolerability and Pharmacokinetics of DAT-1604 Tablets as Monotherapy in the Advanced Solid Tumor
The primary objective of the study is to evaluate the safety, tolerability, PK, and preliminary efficacy of a Polθ Inhibitor DAT-1604 in patients with advanced/metastatic solid tumors, which is refractory to standard therapies, or for which no standard therapies exist.
100 Clinical Results associated with DAT-1604
100 Translational Medicine associated with DAT-1604
100 Patents (Medical) associated with DAT-1604
100 Deals associated with DAT-1604