drugset / Trial / NCT07557446

A Dose REgimen-Finding Study of AGA2115 in Chinese Patients With Osteogenesis ImpeRfecta (EIR)

NCT07557446 ↗

Phase 2 Recruiting 48 enrolled Angitia Biopharmaceuticals Guangzhou Limited
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is to evaluate the safety and efficacy of AGA2115 at three different dose regimens in Chinese adults and adolescents with Type I, III, or IV Osteogenesis imperfecta (OI).

Timeline

Start
2026-06
Primary completion
2028-04
Completion
2029-07

Drugs

EvaluationDrugModalityDoseRoute
Subject AGA2115 Unknown — Subcutaneous