Safety and Clinical Outcomes in Hunter Syndrome Patients 5 Years of Age and Younger Receiving Idursulfase Therapy

This study has been completed.
Sponsor:
Collaborators:
Covance
PharmaNet
PRA Health Sciences
Information provided by (Responsible Party):
Shire
ClinicalTrials.gov Identifier:
NCT00607386
First received: January 22, 2008
Last updated: June 9, 2014
Last verified: February 2014

January 22, 2008
June 9, 2014
December 2007
July 2011   (final data collection date for primary outcome measure)
Safety Evaluation [ Time Frame: 53 weeks ] [ Designated as safety issue: Yes ]
Incidence of adverse events (including infusion-related adverse events), changes in 12-lead ECG, vital signs, standard laboratory parameters, and anti-idursulfase antibody status. [ Time Frame: One year ] [ Designated as safety issue: Yes ]
Complete list of historical versions of study NCT00607386 on ClinicalTrials.gov Archive Site
  • Mean Change From Baseline to Week 53 in Normalized Urinary Glycosaminoglycan (GAG) Levels (μg/mg Creatinine) [ Time Frame: 53 weeks ] [ Designated as safety issue: No ]
    Analysis of urinary GAG levels was performed at baseline, Week 18, Week 36, and Week 53 as an assessment of the pharmacodynamic effects of Elaprase (idursulfase) in this patient population.
  • Single- and Repeat-Dose Pharmacokinetics - Maximum Observed Serum Concentration (Cmax) [ Time Frame: Weeks 1 and 27 ] [ Designated as safety issue: No ]
  • Single- and Repeat-Dose Pharmacokinetics - Time of Maximum Observed Serum Concentration (Tmax) [ Time Frame: Weeks 1 and 27 ] [ Designated as safety issue: No ]
  • Single- and Repeat-Dose Pharmacokinetics - Area Under the Serum Concentration-Time Curve From Time 0 to the Final Time Point With a Concentration ≥ LOQ (AUClast) [ Time Frame: Weeks 1 and 27 ] [ Designated as safety issue: No ]
  • Single- and Repeat-Dose Pharmacokinetics - Area Under the Serum Concentration-Time Curve From Time 0 to Infinity (AUCinf) [ Time Frame: Weeks 1 and 27 ] [ Designated as safety issue: No ]
  • Single- and Repeat-Dose Pharmacokinetics - Elimination Half-Life (t1/2) [ Time Frame: Weeks 1 and 27 ] [ Designated as safety issue: No ]
  • Single- and Repeat-Dose Pharmacokinetics - Mean Residence Time From Time 0 to Infinity (MRTinf) [ Time Frame: Weeks 1 and 27 ] [ Designated as safety issue: No ]
  • Single- and Repeat-Dose Pharmacokinetics - Clearance (CL) [ Time Frame: Weeks 1 and 27 ] [ Designated as safety issue: No ]
  • Single- and Repeat-Dose Pharmacokinetics - Volume of Distribution at Steady State (Vss) [ Time Frame: Weeks 1 and 27 ] [ Designated as safety issue: No ]
  • Mean change from Baseline to Week 53 in urinary GAG clearance (normalized for μg GAG/mg creatinine) [ Time Frame: One year ] [ Designated as safety issue: No ]
  • Single-dose and repeat-dose pharmacokinetic parameters [ Time Frame: Weeks 1 and 27 ] [ Designated as safety issue: No ]
Not Provided
Not Provided
 
Safety and Clinical Outcomes in Hunter Syndrome Patients 5 Years of Age and Younger Receiving Idursulfase Therapy
A Multi-Center, Open-Label Study Evaluating Safety and Clinical Outcomes in Hunter Syndrome Patients 5 Years of Age and Younger Receiving Idursulfase Enzyme Replacement Therapy

The objective of this study is to determine the safety of once weekly dosing of idursulfase 0.5 mg/kg administered by intravenous (IV) infusion for male Hunter syndrome patients ≤ 5 years old.

This study will provide a basis for evaluating the safety of idursulfase administered to Hunter syndrome patients who are ≤ 5 years old. Additionally, this study will provide a basis for evaluating the idursulfase single- and repeated-dose pharmacokinetic profiles as well as the pharmacodynamic effect (as measured by urinary GAG excretion) in this pediatric population. Additional exploratory measures will include abdominal ultrasound measurements of liver and spleen volumes, assessments of growth with comparisons to normal population growth data, assessments of annualized growth velocity, assessments of routine developmental milestones using the Denver II, and assessments of clinical events, including the first occurrence of certain hearing-related events (e.g., hearing loss, otitis media), respiratory-related events (e.g., upper and lower respiratory infections), and specific surgical procedures (e.g., adenoidectomy, placement of PE tubes).

All patients in this open-label study will receive once-weekly infusions of idursulfase at a dose of 0.5 mg/kg.

Interventional
Phase 4
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Hunter Syndrome
  • Mucopolysaccharidosis II
  • MPS II
Biological: Idursulfase
Solution for intravenous infusion, 0.5 mg/kg weekly
Other Name: Elaprase
Idursulfase
Open-label treatment with idursulfase
Intervention: Biological: Idursulfase

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
28
July 2011
July 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • The patient has a diagnosis of Hunter syndrome based upon biochemical criteria either documented in their medical history or established at Screening:

    1. A deficiency in iduronate-2-sulfatase (I2S) enzyme activity of ≤ 10 % of the lower limit of the normal range as measured in plasma, fibroblasts, or leukocytes (based on normal range of measuring laboratory)

      AND

    2. A normal enzyme activity level of one other sulfatase as measured in plasma, fibroblasts, or leukocytes (based on normal range of measuring laboratory).
  • The patient is 5 years of age and under.
  • The patient is male.
  • The patient's parent(s), or patient's legal guardian must have voluntarily signed an Institutional Review Board approved informed consent form after all relevant aspects of the study have been explained and discussed with the patient's parent(s), or the patient's legal guardian.

Exclusion Criteria:

  • The patient has received treatment with another investigational therapy within 30 days prior to enrollment.
  • The patient has clinically relevant medical condition(s) making implementation of the protocol difficult.
  • The patient has previously received idursulfase.
  • The patient has known hypersensitivity to any of the components of idursulfase.
  • The patient has had a tracheostomy.
Male
up to 5 Years
No
Contact information is only displayed when the study is recruiting subjects
Brazil,   Poland,   Taiwan
 
NCT00607386
HGT-ELA-038, 2007-006044-22
No
Shire
Shire
  • Covance
  • PharmaNet
  • PRA Health Sciences
Study Director: Arian Pano, MD, MPH Shire Human Genetic Therapies, Inc.
Principal Investigator: Roberto Giugliani, MD, PhD Hospital de Clinicas de Porto Alegre
Principal Investigator: Wuh-Liang Hwu, MD, PhD National Taiwan University Hospital
Principal Investigator: Anna Tylki-Szymanska, MD, PhD Instytut Pomnik Centrum Zdrowia Dziecka
Shire
February 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP