Viewing Study NCT05576792


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Study NCT ID: NCT05576792
Status: COMPLETED
Last Update Posted: 2025-03-25
First Post: 2022-10-10
Is Gene Therapy: True
Has Adverse Events: False

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

Study Type: OBSERVATIONAL
Expanded Access Type Individual: None
Expanded Access Type Intermediate: None
Expanded Access Type Treatment: None
Patient Registry: False
Target Duration: None
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Bio Spec Retention: None
Bio Spec Description: None
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