Atlas Trials

A 24-week Study Evaluating the Effectiveness and Safety of Lucentis® 0.2mg in Retinopathy of Prematurity Participants in China

Clinical trial NCT05576792 · COMPLETED

Trial details

NCT number
NCT05576792
Sponsor
Novartis Pharmaceuticals
Status
COMPLETED
Study type
OBSERVATIONAL
Retinopathy of Prematurity
Start date
2023-01-13
Primary completion
2024-07-10
Enrollment
62

View on ClinicalTrials.gov

Track trials programmatically

Sponsors, conditions and status changes through the Atlas API.