A PHASE 2, MULTI-CENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, DOSERANGING STUDY TO EVALUATE THE SAFETY AND EFFICACY OF AGA2115 IN ADULTS WITH TYPE I, III, OR IV OSTEOGENESIS IMPERFECTA (OI)

Registry ID

ACT24-001

Source registry

HEALTH_CANADA

Status

Ongoing

Phase

PHASE2

Study type

INTERVENTIONAL

Sponsor

ANGITIA INCORPORATED LIMITED

Start date

2026-04-14

Last update

2025-09-23

Conditions

• OSTEOGENESIS IMPERFECTA

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