drugset / Trial / NCT06125171

Tucidinostat Plus Apatinib for Advanced Osteosarcoma

NCT06125171 ↗

NaSingle-groupOpen-labelTreatment

Summary

This phase II study was designed to assess the efficacy and safety of the combination of Apatinib, Tucidinostat (chidamide), a histone deacetylase inhibitor in relapsed or refractory osteosarcoma patients.

Timeline

Start
2024-01
Primary completion
2024-12
Completion
2025-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Rivoceranib Small molecule 250 mg —
Subject Rivoceranib Small molecule 500 mg —
Subject Tucidinostat Small molecule 0.5 mg/kg Oral
Subject Tucidinostat Small molecule 30 mg Oral

Indications