Secondary identifiers
interventional
N/A
3 countries
3
To establish the effective dose of losartan in patients aged 16 years and above with Osteogenisis Imperfecta, based on maximal reduction in the bone resorption marker carboxy-terminal crosslink of type I collagen telopeptide (CTX)
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
Not reported
Date not reportedClick on a node to explore related trials.
Some registry-reported names shown below are not yet linked in this graph.
Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
November 4, 2024
Actual (reported)Percentage change in CTX from baseline to week 24
Percentage change in CTX from baseline to week 8
Percentage change in TGFβ & P1NP from baseline to week 8 and w24
Change in DXA LSaBMD from baseline to w24
Change in radial and tibial total vBMD by HRpQCT from baseline to w24
Change in Timed Up and Go test from baseline to w24
Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.
Istituto Ortopedico Rizzoli
Bologna, 40136, Italy
Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico
Milan, 20122, Italy
Isala Klinieken Stichting
Zwolle, 8025 AB, Netherlands
Arianna Ferretti Cherkes Zade
First Submitted
November 4, 2024
Download the complete CTIS (EMA) record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.
Source: European Medicines Agency (EMA), Clinical Trials Information System (CTIS). Original record and public documents are available on CTIS.
JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.
Source retrieved:
A Dose REgimen-Finding Study of AGA2115 in Chinese Patients With Osteogenesis ImpeRfecta (EIR)
Contact the study team to confirm eligibility.