drugset / Trial / NCT05508373

A Clinical Study to Evaluate the Safety, Tolerability,JS019 in Patients With Advanced Solid Tumors

NCT05508373 ↗

Phase 1 Unknown 72 enrolled Suzhou Kebo Ruijun Biotechnology Co., Ltd
NaSingle-groupOpen-labelTreatment

Summary

This is a phase 1 clinical study to evaluate the safety, tolerability, pharmacokinetics and preliminary efficacy of JS019 as monotherapy in patients with advanced malignant solid tumors The study includes JS019 monotherapy dose escalation, dose expansion stages to investigate the safety, tolerability, pharmacokinetics and preliminary anti-tumor efficacy of JS019 as monotherapy.

Timeline

Start
2022-03-29
Primary completion
2024-06-15
Completion
2024-08-10

Drugs

EvaluationDrugModalityDoseRoute
Subject JS019 Monoclonal antibody 0.3 mg/kg Intravenous
Subject JS019 Monoclonal antibody 1 mg/kg Intravenous
Subject JS019 Monoclonal antibody 3 mg/kg Intravenous
Subject JS019 Monoclonal antibody 10 mg/kg Intravenous

Indications