Phase 3 Study to Compare Safety and Efficacy of Smoflipid 20% to Intralipid 20% in Hospitalized Neonates and Infants

What is the purpose of this trial?

To show the superiority in safety of Smoflipid over Intralipid® as measured by the number of study patients in each treatment group with conjugated bilirubin exceeding 2 mg/dL during the first 28 days of study treatment, confirmed by a second sample collected 7 days after the first sample.

Gender: Both

Fresenius Kabi DEutschland GmbH

Start Date: 07/07/2017

End Date: 10/31/2017

Last Updated: 02/22/2018

Study HIC#: 1510016597

Get Involved

For more information about this study, contact:
Christine H Mulvey
+1 203-688-2320

If you would prefer to contact a member of the Help us Discover team about this trial and other similar trials, please email or call 1-877-978-8348.

Trial Image


Orly Levit

Principal Investigator