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To provide Omegaven® as a compassionate treatment for critically ill infants with parenteral nutrition associated cholestasis
An intermediate population, Investigational New Drug study, to provide an alternate intravenous fat nutrition, Omegaven®, to help improve liver function while providing adequate nutrition for critically ill infants with parenteral nutrition associated cholestasis
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Drug - Omegaven® | Experimental | Therapy with Omegaven® will be initiated at the goal dose of 0.5-1/kg/day. The default is over 24 hours, but shorter intervals may be considered if a program of total parenteral nutrition cycling is recommended. Omegaven® will be infused intravenously through either a central or peripheral catheter. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Omegaven | Drug | Omegaven® fat emulsion will be used as a compassionate use treatment for critically ill infants with parenteral nutrition associated liver injury |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participant With Decrease in Direct Bilirubin Level | Number of participant with decrease in direct bilirubin levels within 30 days of treatment | First month of treatment |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participant With Resolution of Direct Hyperbilirubinemia | Number of participant with Direct bilirubin level of <2mg/dL at discontinuation of treatment | 2 months |
| Number of Participant With Preservation of Length |
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Inclusion Criteria:
Exclusion Criteria:
Known causes of cholestasis other than parenteral nutrition-associated liver disease including but not limited to Hepatitis C, Cystic fibrosis, biliary atresia, and alpha 1 antitrypsin deficiency are present, prior to Omegaven® initiation
Known fish or egg allergy
Any of the contraindications to use of Omegaven®:
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| Name | Affiliation | Role |
|---|---|---|
| Thao Ho, DO | University of South Florida | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| USF Health | Tampa | Florida | 33606 | United States |
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Infants were screened based on inclusion and exclusion criteria. When there was a potential candidate, an IND application is submitted to FDA.
Infants were recruited from a single NICU for compassionate use of Omegaven for cholestasis.
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| ID | Title | Description |
|---|---|---|
| FG000 | Drug - Omegaven® | Participants were screened based on inclusion and exclusion criteria. If and when a participant was qualified for Omegaven treatment, we sent FDA and application for IND approval. After the approval, the participant received Omegaven daily per protocol until cholestatsis resolved. |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Drug - Omegaven® | These infants were more than one month old with history of long-term TPN dependence due to intestinal problem. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Number of Participant With Decrease in Direct Bilirubin Level | Number of participant with decrease in direct bilirubin levels within 30 days of treatment | Posted | Count of Participants | Participants | First month of treatment |
|
|
2 months
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Drug - Omegaven® | Omegaven treatment group | 0 |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Thao Ho | University of South Florida | 813-844-3437 | tho1@usf.edu |
| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | May 1, 2018 | Jul 6, 2020 | Prot_001.pdf |
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| ID | Term |
|---|---|
| D002779 | Cholestasis |
| D006963 | Hyperphagia |
| D008107 | Liver Diseases |
| ID | Term |
|---|---|
| D001649 | Bile Duct Diseases |
| D001660 | Biliary Tract Diseases |
| D004066 | Digestive System Diseases |
| D012817 | Signs and Symptoms, Digestive |
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| ID | Term |
|---|---|
| C568345 | fish oil triglycerides |
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Monitoring of weekly length while the patient is receiving Omegaven® treatment
| Weekly measurement during treatment. Evaluation every 30 days from treatment initiation until discontinuation of treatment, patient hospital discharge, whichever comes first, or up to 6 months following initiation of treatment |
| Number of Participant With Preservation of Head Circumference | Monitoring of weekly head circumference while the patient is receiving Omegaven® treatment | Weekly measurement during treatment. Evaluation every 30 days from treatment initiation until discontinuation of treatment, patient hospital discharge, whichever comes first, or up to 6 months following initiation of treatment |
| Number of Participant With Preservation of Normal Weight Gain | Monitoring of daily weight gain while the patient is on Omegaven® | Weekly measurement during treatment. Evaluation every 30 days from treatment initiation until discontinuation of treatment, patient hospital discharge, whichever comes first, or up to 6 months following initiation of treatment |
| days |
|
| Sex: Female, Male | Count of Participants | Participants | No |
|
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Region of Enrollment | Count of Participants | Participants |
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| Secondary | Number of Participant With Resolution of Direct Hyperbilirubinemia | Number of participant with Direct bilirubin level of <2mg/dL at discontinuation of treatment | Posted | Count of Participants | Participants | 2 months |
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|
|
| Secondary | Number of Participant With Preservation of Length | Monitoring of weekly length while the patient is receiving Omegaven® treatment | Posted | Count of Participants | Participants | Weekly measurement during treatment. Evaluation every 30 days from treatment initiation until discontinuation of treatment, patient hospital discharge, whichever comes first, or up to 6 months following initiation of treatment |
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|
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| Secondary | Number of Participant With Preservation of Head Circumference | Monitoring of weekly head circumference while the patient is receiving Omegaven® treatment | Posted | Count of Participants | Participants | Weekly measurement during treatment. Evaluation every 30 days from treatment initiation until discontinuation of treatment, patient hospital discharge, whichever comes first, or up to 6 months following initiation of treatment |
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| Secondary | Number of Participant With Preservation of Normal Weight Gain | Monitoring of daily weight gain while the patient is on Omegaven® | Posted | Count of Participants | Participants | Weekly measurement during treatment. Evaluation every 30 days from treatment initiation until discontinuation of treatment, patient hospital discharge, whichever comes first, or up to 6 months following initiation of treatment |
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| 2 |
| 0 |
| 2 |
| 0 |
| 2 |
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| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |