Status:
TERMINATED
A Study to Evaluate the Long-Term Efficacy and Safety of BMN 110 in Patients With Mucopolysaccharidosis IVA (Morquio A Syndrome)
Lead Sponsor:
BioMarin Pharmaceutical
Conditions:
MPS IV A
Mucopolysaccharidosis IVA
Eligibility:
All Genders
Phase:
PHASE1
PHASE2
Brief Summary
This multicenter, open-label extension study is designed to assess long-term efficacy and safety of 2.0 milligrams (mg)/kilogram(kg)/week of BMN 110 in patients diagnosed with Mucopolysaccharidosis IV...
Eligibility Criteria
Inclusion
- Willing and able to provide written, signed informed consent, or in the case of patients under the age of 18 (or 16 years, depending on the region), provide written assent (if required) and written informed consent by a legally authorized representative after the nature of the study has been explained, and prior to any research-related procedures.
- Sexually active patients must be willing to use an acceptable method of contraception while participating in the study.
- Females of childbearing potential must have a negative pregnancy test at Baseline and be willing to have additional pregnancy tests during the study.
- Must have enrolled in a prior BioMarin sponsored clinical study of BMN 110.
Exclusion
- Pregnant or breastfeeding at Baseline or planning to become pregnant (self or partner) at any time during the study.
- Use of any investigational product (other than BMN 110 in a prior clinical study) or investigational medical device within 30 days prior to Baseline, or requirement for any investigational agent prior to completion of all scheduled study assessments.
- Concurrent disease or condition, including but not limited to symptomatic cervical spine instability, clinically significant spinal cord compression, or severe cardiac disease that would interfere with study participation or safety as determined by the Investigator.
- Any condition that, in the view of the Investigator, places the patient at high risk of poor treatment compliance or of not completing the study.
- Were enrolled in MOR-004 (patients from MOR-004 may be eligible to participate in a separate, appropriately designed, extension study).
Key Trial Info
Start Date :
November 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2014
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT01242111
Start Date
November 1 2010
End Date
July 1 2014
Last Update
September 30 2015
Active Locations (4)
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1
Birmingham, United Kingdom, United Kingdom
2
Dumfries, United Kingdom, United Kingdom
3
London, United Kingdom, United Kingdom
4
Manchester, United Kingdom, United Kingdom