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Phase 4 N=16 Randomized Treatment

Study of Glycerol Phenylbutyrate & Sodium Phenylbutyrate in Phenylbutyrate Naïve Patients With Urea Cycle Disorders (UCDs)

Urea Cycle Disorder

Enrolled (actual)
16
Serious AEs
16.2%
Results posted
Jul 2023
Primary outcome: Primary: Rate of Treatment Success (Percentage of Participants Defined as Treatment Success at Week 4) During the Initial Treatment Period — 81.8; 80.0 percentage of participants — p=1.0000

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
RAVICTI (Drug); NaPBA (Drug)
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
Amgen
Primary completion
Jul 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Rate of Treatment Success (Percentage of Participants Defined as Treatment Success at Week 4) During the Initial Treatment Period
81.8; 80.0 1.0000
SECONDARY
Rate of Drug Discontinuations (Percentage of Participants Who Discontinued Study Drug) Due to Any Reason in the Initial Treatment Period
0; 0
SECONDARY
Change From Baseline in Fasting Plasma Ammonia Levels During the Initial Treatment Period
6.5; 0.0; 25.5; -10.4; 7.4; -10.9 0.8464
SECONDARY
Plasma Ammonia Area Under the Curve (AUC) 0 to 8h at the End of the Initial Treatment Period
331.8; 258.9 0.8579
SECONDARY
Peak Plasma Concentration (Cmax) of Ammonia at the End of the Initial Treatment Period
60.2; 38.1 0.7155

Summary

This is a randomized, controlled, open-label parallel arm study to assess the safety, tolerability, pharmacokinetics and ammonia control, of RAVICTI® as compared to Sodium phenylbutyrate (NaPBA) in urea cycle disorder subjects not currently or previously chronically treated with phenylacetic acid (phenylacetate; PAA) prodrugs. The study design will include: 1) Baseline Period; 2) Initial Treatment Period; 3) a RAVICTI only Transition Period 4) a RAVICTI only Maintenance Period; and 5) a RAVICTI only Safety Extension Period. The study will run for approximately 25 weeks.

Eligibility Criteria

Inclusion Criteria

  • Signed informed consent given by the subject or the subject's parent/legal guardian for those under 18 years of age or the age of consent by local regulation.
  • Male and female subjects with a suspected or confirmed UCD diagnosis of any subtype, except n-acetylglutamate synthetase (NAGS) deficiency.
  • Suspected diagnosis is defined as having experienced a hyperammonemic crisis (HAC) or a documented high ammonia of >=100 µmol/L
  • Confirmed diagnosis is determined via enzymatic, biochemical, or genetic testing.
  • Requires nitrogen-binding agents according to the judgment of the Investigator
  • Birth and older.
  • All females of childbearing potential and all sexually active males must agree to use an acceptable method of contraception from signing the informed consent throughout the study and for 30 days after the last dose of study drug. Acceptable forms of contraception are (oral, injected, implanted or transdermal), tubal ligation, intrauterine device, hysterectomy, vasectomy, or double barrier methods. Abstinence is an acceptable form of birth control, though appropriate contraception must be used if the subject becomes sexually active.

Exclusion Criteria

  • Subject has received chronic treatment with an oral phenylbutyrate (RAVICTI, NaPBA, Pheburane, or other) longer than 14 consecutive days within one year prior to enrollment.
  • Temporary use of NaPBA for acute management of a hyperammonemic crisis in the past is acceptable.
  • Any concomitant illness (e.g., malabsorption or clinically significant liver or bowel disease) which would preclude the subject's safe participation, as judged by the Investigator.
  • Has undergone liver transplantation, including hepatocellular transplant.
  • Subjects on sodium benzoate (NaBz) at Baseline will be excluded if they are viewed by the Investigator as being unable to undergo NaBz transition to a PAA prodrug during the Initial Treatment Period.
  • Known hypersensitivity to phenylbutyric acid (PBA) or any excipients of the NaPBA/PBA formulations.
  • Pregnant or breast-feeding patients. Women of childbearing potential must have a pregnancy test performed at the Baseline Visit prior to the start of study drug.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03335488). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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