IGF-1/IGFBP3 Prevention of Retinopathy of Prematurity
Completed
Shire
Phase 2
2010-06-18
To compare the severity of retinopathy of prematurity (ROP) among treated infants with an
untreated control population, matched for gestational age at birth while confirming the dose
of rhIGF-1/rhIGFBP-3 is safe and efficacious.
Long-term Safety and Efficacy Outcome Study Comparing Children Previously Enrolled in Study ROP-2008-01 for the Prevention of Retinopathy of Prematurity (ROP)
Active, not recruiting
Shire
Phase 2
2015-03-26
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 (Section D) (NCT01096784).
A Clinical Efficacy and Safety Study of SHP607 in Preventing Chronic Lung Disease in Extremely Premature Infants
Active, not recruiting
Shire
Phase 2
2019-05-09
The purpose of this study is to determine if an investigational drug can reduce the burden of
chronic lung disease in extremely premature babies through 12 months corrected age (CA), as
compared to extremely premature babies receiving standard neonatal care alone.
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