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Clinical Trial Summary

The main purpose of this study is to evaluate the long-term efficacy and safety outcomes following short-term exposure to rhIGF-1/rhIGFBP-3 versus standard neonatal care in Study ROPP-2008-01 (NCT01096784).


Clinical Trial Description

Long-term Safety and Efficacy Outcome Study Comparing Children Previously Enrolled in Study ROPP-2008-01 for the Prevention of Retinopathy of Prematurity (ROP) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02386839
Study type Interventional
Source Takeda
Contact
Status Completed
Phase Phase 2
Start date March 26, 2015
Completion date September 28, 2021

See also
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