Compassionate Use of Omegaven in the Treatment of Parenteral Nutrition Induced Hepatic Injury



Status:Completed
Conditions:Gastrointestinal
Therapuetic Areas:Gastroenterology
Healthy:No
Age Range:Any - 10
Updated:2/8/2019
Start Date:August 2013
End Date:February 5, 2019

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This study is being done to determine if an investigational study drug called Omegaven can
help to improve liver disease thought to be caused by Total Parenteral Nutrition (TPN). TPN
is intravenous feeding (IV feeding tube) that provides patients the nutrients when they are
unable to drink fluid or eat food by mouth.

PAtients with direct bilirubin >2gm/dL and short bowel syndrome are eligible for enrollment.
Omegaven at 1gm/kg/day will be administered via central venous line instead of standard lipid
preparations.

Inclusion Criteria:

1. Patients must be 2 months -10 years of age

2. Patients who are PN dependent (unable to meet nutritional needs solely by enteral
nutrition) and are expected to require PN for at least another 30 days

3. Patients considered eligible for study participation must have parenteral nutrition
associated liver disease (PNALD) as defined by a direct bilirubin of >2.0mg/dL. Other
causes of liver disease should be excluded. A liver biopsy is not necessary for
treatment

4. 2 consecutive direct bilirubin test results >2.0mg/dl

5. The patient must have failed standard therapies to prevent the progression of liver
disease such as surgical treatment, cyclic TPN, avoiding overfeeding,
reduction/removal of copper and manganese from TPN, advancement of enteral feeding,
and use of ursodiol (Actigall)

6. Subjects who are currently under treatment for PNALD with Compassionate Use Omegaven
and have a direct Bilirubin of< 2, but who remain TPN dependent and require continued
therapy with Omegaven

Exclusion Criteria:

1. Other known causes of chronic liver disease (hepatitis C, cystic fibrosis, biliary
atresia and alpha 1 anti-trypsin deficiency)

2. Enrollment in any other clinical trial involving an investigational agent (unless
approved by the designated physicians on the multidisciplinary team)

3. The parent, guardian, or child is unwilling to provide consent or assent

4. Allergy to any fish product, egg protein, and/or previous allergy to Omegaven

5. Active coagulopathies characterized by on-going bleeding or by a requirement for
clotting factor replacement such as fresh frozen plasma or cryoprecipitate to maintain
homeostasis

6. Impaired lipid metabolism or severe hyperlipidemia with or without pancreatitis

7. Unstable diabetes mellitus

8. Stroke/embolism

9. Collapse and shock

10. Undefined coma status

11. Active infection at time of initiation of Omegaven® up until such time as child is
afebrile with stable vital signs and one negative 48 hour culture
We found this trial at
1
site
1935 Medical District Dr
Dallas, Texas 75235
(214) 456-7000
Children's Medical Center of Dallas Children's Medical Center is private, not-for-profit, and is the fifth-largest...
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mi
from
Dallas, TX
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