Official Title
A Multicenter, Open-label BMN 110 US Expanded Access Program (BMN 110 US EAP) to Provide BMN 110 to Patients Diagnosed With MPS IVA
Brief Summary

The Expanded Access Program (EAP) is an open-label, multicenter program to: 1. Provide patients who have been diagnosed with Mucopolysaccharidosis IVA (MPS IVA) access to BMN 110 until commercial product is available 2. Collect additional information on the safety and tolerability of BMN 110 administration in patients with MPS IVAPatients enrolled in the EAP will receive 2.0 mg/kg intravenous infusions of BMN 110every week during the program.

Approved for marketing
Mucopolysaccharidosis IVA
Morquio A Syndrome
MPS IVA

Drug: BMN 110

Eligibility Criteria

Inclusion Criteria:

- Diagnosed with MPS IVA as confirmed by either N-acetylgalactosamine-6-sulfatase
(GALNS) enzymatic test (GALNS activity in affected range, beta-galactosidase and a
second lysosomal sulfatase activity within normal range) or molecular diagnostic
test (two mutations in GALNS identified that have previously been associated with an
enzyme defect).

- Willing and able to provide written, signed informed consent, or in the case of
patients under the age of 18, provide written assent (as required by the IRB) and
written informed consent by a legally authorized representative after the nature of
the program has been explained, and prior to any program assessments or evaluations.

- Sexually active patients must be willing to use an acceptable method of
contraception while participating in the program.

- Females of childbearing potential must have a negative pregnancy test at Baseline
and be willing to have additional pregnancy tests during the program.

- Willing and able to comply with all program procedures.

Exclusion Criteria:

- Pregnant or breastfeeding at Baseline or planning to become pregnant (self or
partner) at any time during the program. Patients who become pregnant during the
program will be discontinued from the program.

- Currently enrolled in an ongoing clinical study of BMN 110.

- Discontinued from a BMN 110 clinical study secondary to a safety-related event.

- Use of any investigational product (other than BMN 110 in a clinical study) or
investigational medical device within 30 days prior to Baseline, or requirement for
any investigational agent prior to completion of all scheduled program assessments.

- Not a current US resident or expecting to have travel plans outside the US during
the planned period of participation in the Expanded Access Program (EAP) that may
interfere with dosing regimen, scheduled program visits and safety monitoring.

- Any condition that, in the view of the Investigator or sponsor, places the patient
at high risk of poor treatment compliance or of not completing the EAP.

Eligibility Gender
All
Eligibility Age
Minimum: N/A ~ Maximum: N/A
Countries
Puerto Rico
United States
Locations

Birmingham, Alabama, United States

Little Rock, Arkansas, United States

Oakland, California, United States

Orange, California, United States

Aurora, Colorado, United States

Washington, District of Columbia, United States

Hollywood, Florida, United States

Miami, Florida, United States

Atlanta, Georgia, United States

Chicago, Illinois, United States

Louisville, Kentucky, United States

New Orleans, Louisiana, United States

Minneapolis, Minnesota, United States

Paterson, New Jersey, United States

Manhasset, New York, United States

New York, New York, United States

Portland, Oregon, United States

Philadelphia, Pennsylvania, United States

Pittsburgh, Pennsylvania, United States

Nashville, Tennessee, United States

Houston, Texas, United States

Salt Lake City, Utah, United States

Seattle, Washington, United States

Tacoma, Washington, United States

Santurce, Puerto Rico

BioMarin Pharmaceutical
NCT Number
Keywords
Mucopolysaccharidosis IVA Type A
MPS IVA Type A
Mucopolysaccharidosis IVA
MPS IVA
Morquio A Syndrome
Lysosomal Storage Disorder
LSD
N-acetylgalactosamine-6-sulfatase
N-acetylgalactosamine-6-sulfate
MeSH Terms
Mucopolysaccharidoses
Mucopolysaccharidosis IV