drugset / Trial / NCT05423262

A Study of TRK-950 in Patients With Advanced Solid Tumors

NCT05423262

Phase 1/2 Recruiting 49 enrolled Toray Industries, Inc
Non-randomizedSingle-groupOpen-labelTreatment

Summary

Part 1 • To determine the safety and tolerability of TRK-950 in patients with advanced solid tumors Part 2 • To determine the safety and tolerability of TRK-950 in combination with nivolumab(NIVO) in patients with advanced solid tumors eligible for NIVO therapy Part 3 • To determine the efficacy of TRK-950 in patients with advanced/recurrent unresectable melanoma, who received prior chemotherapy with dacarbazine(DTIC) and for whom no standard therapy exists

Timeline

Start
2022-07-06
Primary completion
2027-12
Completion
2027-12

Drugs

EvaluationDrugModalityDoseRoute
Subject TRK-950 Monoclonal antibody 5 mg/kg Intravenous
Subject TRK-950 Monoclonal antibody 10 mg/kg Intravenous
Subject TRK-950 Monoclonal antibody 20 mg/kg Intravenous
Background Nivolumab Monoclonal antibody 240 mg Intravenous

Indications