drugset / Trial / NCT06739213

A Phase II Study of SYHA1813 for Recurrent or Progressive High-Grade Meningioma

NCT06739213

Phase 2 Not yet recruiting 56 enrolled Shanghai Runshi Pharmaceutical Technology Co., Ltd
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a randomized, controlled, open-label, multicenter, Phase II clinical study designed to evaluate the efficacy and safety of SYHA1813 compared to investigators' choice in participants with recurrent or progressive high-grade meningioma.

Timeline

Start
2025-01-31
Primary completion
2027-01-31
Completion
2028-01-13

Drugs

EvaluationDrugModalityDoseRoute
Subject SYHA1813 Unknown 20 mg

Indications