Extension Study for Patients Who Have Participated in a BMN 701 Study
- Conditions
- Pompe Disease
- Interventions
- Biological: BMN 701
- Registration Number
- NCT01435772
- Lead Sponsor
- BioMarin Pharmaceutical
- Brief Summary
This is a Phase 2 open-label, multiple dose study of BMN 701 administered by IV infusion every 2 weeks (qow) to patients with late-onset Pompe disease.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 21
- Have completed a prior BMN 701 clinical development study;
- Have provided written informed consent after the nature of the study has been explained prior to performance of any study-related procedures. Minors may participate as long as they provide written assent after the nature of the study has been explained to them and after their parent, or legal guardian has provided written informed consent, prior to the performance of any study-related procedures;
- Have been diagnosed with late-onset Pompe Disease, based on the entry criteria of a prior BMN 701 study;
- If sexually active, be willing to use 2 known effective methods of contraception from Screening until 4 months after the last dose of study-drug;
- If female, and not considered to be of childbearing potential, be at least 2 years post-menopausal, or have had tubal ligation at least 1 year prior to screening, or have had a total hysterectomy;
- If female, and of childbearing potential, have a negative pregnancy test during the Screening Period and at the Baseline visit, and be willing to have additional pregnancy tests during the study;
- Have the ability to comply with the protocol requirements, in the opinion of the Investigator.
- Have received any experimental or approved therapy for Pompe disease, other than BMN 701, subsequent to completion of a BMN 701 study and prior to entry into POM-002;
- Have received, or are anticipated to receive, any investigational medication, other than BMN 701, within 30 days prior to the first dose of study-drug;
- Are breastfeeding at screening or planning to become pregnant (self or partner) at any time during the study;
- Have a medical condition or extenuating circumstance that, in the opinion of the Investigator, might compromise the patient's ability to comply with the protocol requirements or compromise the patient's well being or safety.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description BMN 701 20mg/kg BMN 701 BMN 701 20mg/kg IV every other week BMN 701 5mg/kg BMN 701 BMN 701 5mg/kg IV every other week BMN 701 10mg/kg BMN 701 BMN 701 10mg/kg IV every other week
- Primary Outcome Measures
Name Time Method Number of Participants With a Positive Anti-BMN 701 Antibody Baseline, Week 144 Status of Anti-BMN 701 antibody is corresponding to the test results of blood samples.
Number of Participants With a Positive Anti-BMN 701 Antibody Response Baseline, Week 144 Status of Anti-IGF-II antibody is corresponding to the test results of blood samples
- Secondary Outcome Measures
Name Time Method Change From Baseline in Urine Tetrasaccharide Concentration at Week 144 Baseline, Week 144 Change from Baseline in Urine Tetrasaccharide Concentration at Week 144
Percent Predicted Maximal Inspiratory Pressure (MIP) Baseline, Week 144 Pulmonary Function Test: Percent Predicted Maximal Inspiratory Pressure
6 Minutes Walk Test (Meters) Baseline, Week 144 Distance walked within 6 minutes
Percent Predicted Upright Forced Vital Capacity (FVC) Baseline, Week 144 Pulmonary function test: Percent Predicted Upright Forced Vital Capacity
Plasma IGF-I Concentration Baseline, Week 144 Plasma IGF-I concentration from lab
Percent Predicted Maximum Expiratory Pressure (MEP) Baseline, Week 144 Pulmonary Function Test: Percent Predicted Maximum Expiratory Pressure
Insulin-like Growth Factor Binding Protein 3 (IGFBP3) Baseline, Week 144 insulin-like growth factor binding protein 3 from lab
Maximum Voluntary Ventilation (MVV) Baseline, Week 144 Pulmonary function test: Maximum Voluntary Ventilation (MVV)
Plasma IGF-II Concentration Baseline, Week 144 Plasma IGF-II concentration from lab
Trial Locations
- Locations (12)
Univ of California San Diego School of Medicine
🇺🇸San Diego, California, United States
University of Florida College of Medicine
🇺🇸Gainesville, Florida, United States
Royal Brisbane and Women's Hospital
🇦🇺Herston, Queensland, Australia
Tampa General Hospital
🇺🇸Tampa, Florida, United States
Hôpital Pitié-Salpêtrière
🇫🇷Paris, France
Auckland City and Starship Children's Hospital
🇳🇿Auckland, New Zealand
Villa Metabolica, ZKJM MC University Mainz
🇩🇪Mainz, Germany
Royal Free Hospital
🇬🇧London, United Kingdom
Salford Royal NHS Foundation Trust
🇬🇧Salford, United Kingdom
University Hospitals Birmingham NHS Foundation Trust
🇬🇧Birmingham, United Kingdom
Royal Adelaide Hospital
🇦🇺North Adelaide, South Australia, Australia
University of Kansas Medical Center
🇺🇸Kansas City, Kansas, United States