Official Title
A Phase 1 Study of S-3304 in Patients With Solid Tumors
Phase
Phase 1Lead Sponsor
ShionogiStudy Type
InterventionalStatus
Completed No Results PostedIndication/Condition
Solid TumorsIntervention/Treatment
s-3304 ...Study Participants
32To determine the maximum tolerated dose and safety profile of S-3304 in patients with biopsy accessible cancer who have failed previous therapy or to whom no standard therapies are available. To determine the pharmacokinetic profile of S-3304 in this patient population
Inclusion criteria: Biopsy proven diagnosis of solid tumor(s) with biopsy accessible lesion(s) Must be able to tolerate oral medication Exclusion criteria Patients with other serious illnesses Patients who are receiving treatments