Study of the Safety of HPN (Hyperion)-100 for the Long-Term Treatment of Urea Cycle Disorders (Treat UCD)
- Registration Number
- NCT00947297
- Lead Sponsor
- Amgen
- Brief Summary
This was a long-term safety study HPN-100 in urea cycle disorder (UCD) subjects. Subjects were assessed regularly for safety and control of their venous ammonia. Hyperammonemic events were characterized with respect to contributing factors, such as intercurrent illness, diet, and noncompliance with medication.
- Detailed Description
This was a one year long-term safety study of HPN-100 in UCD subjects. Subjects were assessed regularly for safety and control of their venous ammonia. Hyperammonemic events were characterized with respect to contributing factors, such as intercurrent illness, diet, and noncompliance with medication.
Forty subjects with a diagnosis of UCD who completed Study HPN-100-006 were enrolled.
Twenty additional UCD subjects ≥ 6 years of age were enrolled. These subjects included those who did not qualify for HPN-100-006 \[e.g., subjects between the ages of 6-17; subjects with other UCD subtypes or adult subjects who have not taken sodium phenylbutyrate (NaPBA) in the past 6 months, etc.\]. For adult subjects not receiving NaPBA in the past 6 months, subjects must, in the judgment of the investigator, be anticipated to benefit from the addition of a nitrogen-scavenging agent to their current treatment. See the inclusion criteria for examples of clinical evidence of potential benefit.
Monthly assessments included safety laboratory tests, amino acid panel, vital signs, electrocardiogram (ECG) monitoring, venous ammonia, and blood and urine metabolites. Adverse events (AEs) and concomitant medications were recorded on an ongoing basis.
Study acquired from Horizon in 2024.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 60
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Male and female subjects who completed HPN-100-006:
*Additionally, approximately 20 UCD subjects ≥ 6 years of age may be enrolled who have not participated in HPN-100-006. These subjects may include those who did not qualify HPN-100-006 (e.g., subjects between the ages of 6-17 years, subjects with other UCD subtypes, or adult subjects who have not taken sodium phenylbutyrate (NaPBA) in the past 6 months, etc.). For adult subjects not receiving NaPBA in the past 6 months, subjects must, in the judgment of the investigator, be anticipated to benefit from the addition of a nitrogen-scavenging agent to their current treatment. Clinical evidence of potential benefit from introduction of an ammonia-scavenging agent might include a recent history (in the past year) of clinically overt hyperammonemia accompanied by a venous ammonia ≥ 100 μmol/L, a recent history (within the past year) of protein intolerance, or a history of abnormally high venous ammonia levels accompanied by symptoms (e.g., headache) that might reasonably be attributed to hyperammonemia.
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Signed informed consent by subject and/or subject's legally acceptable representative.
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Diagnosis of urea cycle disorder (enzyme or transporter deficiency) confirmed via enzymatic, biochemical, or genetic testing.
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Able to perform and comply with study activities, including blood draws.
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Negative pregnancy test for all females of childbearing potential.
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All females of childbearing potential and all sexually active males must agree to use an acceptable method of contraception throughout the study.
- Screening venous ammonia level of ≥ 100 μmol/L or signs and symptoms indicative of hyperammonemia; subjects may be re-screened after their venous ammonia is controlled, at the discretion of the investigator.
- History of 4 or more hyperammonemic events as defined in Section 3.5.1 in the preceding 12 months.
- Active infection (viral or bacterial) or any other condition that may increase venous ammonia levels.
- Any clinical or laboratory abnormality or medical condition that, at the discretion of the investigator, may put the subject at increased risk by participating in this study.
- Use of any medication known to significantly affect renal clearance (e.g., probenecid) or to increase protein catabolism (e.g., corticosteroids), or other medication known to increase venous ammonia levels (e.g., valproate), within the 24 hours prior to Day 1 and throughout the study.
- History of QTc (QT interval corrected) prolongation, or a QTc interval ≥ 450 msec or an increase of ≥ 60 msec during the previous HPN-100 study if applicable.
- Known hypersensitivity to PAA or PBA.
- Liver transplant, including hepatocellular transplant.
- Breastfeeding or lactating females.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description HPN-100 HPN-100 Patients who were treated with HPN-100
- Primary Outcome Measures
Name Time Method Rate of Adverse Events (Number of Participants Who Experienced Any AE Considered Related to Study Drug) 1 year
- Secondary Outcome Measures
Name Time Method Blood Ammonia Levels 1 Year Venous Ammonia levels over time
Number and Causes of Hyperammonemic Events 1 year Number of hyperammonemic crises per patient
Patient Satisfaction With HPN-100 Month 1 post dose Drug preference will be noted at week 3
Trial Locations
- Locations (22)
SNBL-Clinical Pharmacology Center
🇺🇸Baltimore, Maryland, United States
Nationwide Children's Hospital
🇺🇸Columbus, Ohio, United States
University of Pittsburgh
🇺🇸Pittsburgh, Pennsylvania, United States
The Hospital for Sick Children
🇨🇦Toronto, Ontario, Canada
University Hospitals Case Medical Center
🇺🇸Cleveland, Ohio, United States
Maine Medical Center
🇺🇸Portland, Maine, United States
Tufts-New England Medical Center
🇺🇸Boston, Massachusetts, United States
Mount Sinai School of Medicine
🇺🇸New York, New York, United States
Univeristy of Iowa
🇺🇸Iowa City, Iowa, United States
Westchester Medical Center
🇺🇸Valhalla, New York, United States
University of Minnesota Medical Center
🇺🇸Minneapolis, Minnesota, United States
Oregon Health & Science University
🇺🇸Portland, Oregon, United States
University of Utah
🇺🇸Salt Lake City, Utah, United States
Medical College of Wisconsin
🇺🇸Milwaukee, Wisconsin, United States
UCLA
🇺🇸Los Angeles, California, United States
Stanford University
🇺🇸Stanford, California, United States
Children's Hospital Colorado
🇺🇸Aurora, Colorado, United States
Children's National Medical Center
🇺🇸Washington, District of Columbia, United States
Long Beach Memorial
🇺🇸Long Beach, California, United States
Baylor College of Medicine
🇺🇸Houston, Texas, United States
Yale School of Medicine
🇺🇸New Haven, Connecticut, United States
University of Florida
🇺🇸Gainesville, Florida, United States