Iduronate-2-sulfatase Enzyme Replacement Therapy in Mucopolysaccharidosis II (MPS II)

Shire

Status and phase

Completed

Phase 3

Phase 2

Conditions

Mucopolysaccharidosis II

Treatments

Biological: Placebo

Biological: Iduronate-2-sulfatase enzyme replacement therapy

Biological: iduronate-2-sulfatase enzyme replacement therapy

Study type

Interventional

Funder types

Industry

Identifiers

NCT00069641

TKT024

Details and patient eligibility

About

The purpose of this study is to determine whether the administration of iduronate-2-sulfatase enzyme in a weekly or every other week therapy frequency is safe and efficacious in patients with MPS II.

Full description

MPS II is a rare, X-linked, lysosomal storage disorder caused by a deficiency in the enzyme iduronate-2-sulfatase. Because of this deficiency, glycosaminoglycans (GAG) accumulate in multiple tissues and organs, resulting in progressive cellular and organ system dysfunction. The purpose of this study is to determine if one year of therapy with iduronate-2-sulfatase enzyme replacement therapy, at a dose of 0.5mg/kg, weekly or every other week, is safe, and results in clinically meaningful improvement in multiple organ function, compared with a placebo group. Upon completion of the study, patients will be eligible to enroll in an open-label maintenance study.

Enrollment

96 patients

Sex

Male

Ages

5 to 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

To be eligible to participate in this study, patients must meet the following inclusion criteria prior to enrollment:

The diagnosis of MPS II will be determined by the investigator based upon both clinical and biochemical criteria.
All patients must have at least one of the following Clinical Criteria considered by the investigator to be MPS II-related:
- Hepatosplenomegaly
- Radiographic evidence of dysostosis multiplex
- Valvular heart disease
- Evidence of obstructive pulmonary disease
In addition, patients must have the following Biochemical Criteria:
- Documented deficiency in iduronate-2-sulfastase enzyme activity of less than or equal to 10% of the lower limit of the normal range as measured in plasma, fibroblasts, or leukocytes (based on normal range of measuring laboratory).
- A normal enzyme activity level of one other sulfatase as measured in plasma, fibroblasts, or leukocytes (based on normal range of measuring laboratory).
Must be male, 5 to 25 years of age.
Forced vital capacity of <80% of predicted obtained at the baseline evaluation of this study.
Must be able to adequately perform the testing required in this study, including reproducible pulmonary function testing by spirometry, as judged by the investigator.
Patient, patient's parent(s), or legally authorized guardian must have voluntarily signed an Institutional Review Board (IRB)/Independent Ethics Committee (IEC)-approved informed consent form after all relevant aspects of the study have been explained and discussed with the patient.

Exclusion criteria

Patients meeting any of the following criteria are not eligible for participation in this study:

Patient has received treatment with another investigational therapy within the past 60 days.
Patient, patient's parent(s), or patient's legal guardian is unable to understand the nature, scope, and possible consequences of the study.
Patient is unable to comply with the protocol (e.g., due to a medical condition such as cervical cord compression or uncooperative attitude) or is unlikely to complete the study, as determined by the investigator.
Patient has a tracheostomy.
Patient has received a bone marrow or cord blood transplant.
Patient with known hypersensitivity to any of the components of iduronate-2-sulfatase.