drugset / Trial / NCT03519074

Cisplatin Combined with Oral TS-1 in Patients with Advanced Solid Tumors with Different Degrees of Liver Dysfunction

NCT03519074 ↗

Phase 2 Active not recruiting 48 enrolled National University Hospital, Singapore
NaSingle-groupOpen-labelBasic science

Summary

The purpose of this study is to formally characterize the pharmacokinetics (PK), safety, and tolerability of TS-1 in combination with cisplatin in adult patients with advanced solid tumors who have mild, moderate or severe hepatic impairment relative to patients with normal hepatic function, as categorized by the United States National Cancer Institute organ dysfunction working group \[NCI-ODWG\] criteria for hepatic dysfunction.

Timeline

Start
2016-07-22
Primary completion
2024-09-01
Completion
2025-12-20

Drugs

EvaluationDrugModalityDoseRoute
Subject TS-1 Small molecule 30 mg/m2 Oral
Background Cisplatin Other / unclassified 60 mg/m2 —

Indications