Dosing Study of Replagal in Patients With Fabry Disease

This study has been completed.
Sponsor:
Collaborator:
Information provided by (Responsible Party):
Baylor Research Institute
ClinicalTrials.gov Identifier:
NCT00068107
First received: September 6, 2003
Last updated: March 19, 2015
Last verified: March 2015
  Purpose

This study will determine the safety and effectiveness of increasing Replagal infusions in certain patients with Fabry disease. Replagal is a genetically engineered form of Alpha-galactosidase A, an enzyme that normally breaks down a fatty substance called globotriaosylceramide (Gb3). In patients with Fabry disease, Alpha-galactosidase A does not function properly and, therefore, Gb3 builds up, causing problems with the kidneys, heart, nerves, and blood vessels.

Patients with Fabry disease who are participating in NIH protocol 00-N-0185 or 02-N-0220 may be eligible for this study. This includes patients who are currently taking Replagal but whose kidney function continues to worsen, or patients who have certain test results that are much improved after Replagal infusion.

Participants will receive Replagal infusions (0.2 mg/kg body weight) through a vein once a week (as opposed to the previous dosage of once every 2 weeks) for up to 2 years. The first infusion, and some others, are given at the NIH Clinical Center, but most are administered by the patient's local doctor. Vital signs are measured before, immediately after, and 1 hour after each infusion.

Baseline evaluations are done on an inpatient basis at the NIH Clinical Center over a 1-week period before and after the first Replagal infusion and at 6-month intervals during the study. Tests include a check of vital signs (temperature, respiratory rate, pulse rate, and blood pressure); weight measurement; physical and neurological examinations; routine blood and urine tests; 24-hour urine collection; electrocardiogram; and review of treatment side effects. In addition, the following tests are done:

  • Quantitative sensory testing: This is a non-invasive test to measure the ability to sense warm, cold and vibration in the hand and foot.
  • QSART: This test measures the amount of sweat in a particular area of skin that did not sweat enough. A small amount of a medicine called acetylcholine is put on the skin and made to enter the skin using a very small electric current.
  • Doppler skin blood flow: This test measures blood flow to the blood vessels of the skin. A machine takes pictures of blood flow in the skin of the forearm using a laser beam. Pictures are taken before and during application of medicines that cause blood vessels to dilate. Acetylcholine is used on one forearm and nitroprusside is used on the other. The medication is made to enter the skin using a small el...

Condition Intervention Phase
Fabry Disease
Drug: Replagal
Phase 2

Study Type: Interventional
Study Design: Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Study of Weekly Dosing Regimens of Replagal in Patients With Fabry Disease With Incomplete Clinical Response to Long-Term Therapy

Resource links provided by NLM:


Further study details as provided by Baylor Research Institute:

Primary Outcome Measures:
  • Estimated Glomerular Filtration Rate (eGFR) [ Time Frame: Relagal was administered every 2 weeks for 2-4 years pre-study, Relagal was administred weekly during the study (approx. 4.5-10 years) ] [ Designated as safety issue: No ]
    The rate of decline in renal function, as measured by estimation of glomerular filtration rate at baseline when participants were receiving agalsidase alfa (Relagal) every 2 weeks and when participants were receiving weekly infusion of Relagal.


Secondary Outcome Measures:
  • Globotriaosylceramide (Gb(3)) in Plasma [ Time Frame: Baseline and last observation (up to 10 years) ] [ Designated as safety issue: No ]
  • Globotriaosylceramide (Gb(3)) in Urine Sediment [ Time Frame: Baseline and last observation (up to 10 years) ] [ Designated as safety issue: No ]
  • Number of Participants With a Change in Quantitative Sudomotor Axon Reflex Test [ Time Frame: Baseline and last observation (up to 10 years) ] [ Designated as safety issue: No ]
    Quantitative sudomotor axon reflex test (QSART) is a measure of sweat function

  • Quantitative Sensory Testing [ Time Frame: pre-study was 2-4 years, during study sensory testing measured for approx. 4.5-5 years ] [ Designated as safety issue: No ]
    For quantitative sensory testing, the outcome variable (detection threshold score) was analyzed for all combinations of location (foot, hand, and thigh) and test (cold, vibration, and warm). Possible threshold scores may range from 1-25. Score values of ">25" were set to 25. Higher scores indicate higher sensory detection threshold. Therefore, lower score is better. Time, measured in years, was centered at the date in which patients switched treatment regimen. All available measurements were used. A linear mixed model analysis was used to test for differences in the linear association between time and detection threshold score pre-and-post ERT regiment change while accounting for the correlation among observations from the same individual. Specifically, the model contained a subject specific random intercept with year as a fixed effect and knot at time of the treatment change.

  • Doppler Skin Blood Flow [ Time Frame: 10 years ] [ Designated as safety issue: No ]

Enrollment: 13
Study Start Date: September 2003
Study Completion Date: December 2013
Primary Completion Date: December 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Relagal
All participants received Relagal administered weekly
Drug: Replagal
enzyme replacement therapy
Other Name: agalsidase alfa

Detailed Description:

Objectives: The goal of this study is to determine whether higher frequency of dosing of enzyme replacement therapy (ERT) can either significantly slow the decline of renal function or continuously sustain the normalization of other objective functions in patients with Fabry disease who have been receiving intravenous infusions of Replagal (agalsidase alfa) at a dose of 0.2 mg/kg of body weight administered every 2 weeks.

Study Population: Patients with Fabry disease who are currently on clinical research protocols 00-N-0185/TKT011 or 02-N-0220/TKT015 and who have demonstrated progressive decline in calculated glomerular filtration rate (GFR) of at least 5 ml/min/year on ERT or who consistently show transient improvement in objective functions (such as sweating) in the few days post-infusion.

Design: This is an open label study comparing one dosing regimen with a previous less intensive dosing regimen. Patients will receive a dose of 0.2 mg/kg of body weight every week.

Outcome Measures: The main outcome measure will be a change in the mean linear rate of decline of the estimated calculated GFR. The main hypothesis is that a more frequent administration of the previous dose of Replagal will significantly reduce the mean slope of the decline of the calculated glomerular filtration rate GFR compared with the currently observed slope on a dose of 0.2 mg/kg administered every 2 weeks. At the 2-year time point, the dose will be increased to 0.4 mg/kg only in the patients whose GFR continues to significantly decline. Secondary outcome measures will be globotriaosylceramide (Gb(3)) in plasma and urinary sediment, quantitative sudomotor axon reflex test, quantitative sensory testing. Study duration is 2 years with a possibility of additional one-year extensions.

  Eligibility

Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Criteria
  • INCLUSION CRITERIA:

Patients with Fabry disease participating in 00-N-0185/TKT011 or 02-N-0220/TKT015 may be eligible. No other Fabry patients will be eligible.

Patients losing GFR at a rate greater than 5 ml/min/year despite ERT with agalsidase alfa for greater than or equal to 2.5 years in 00-N-0185/TKT/003/006/011 Study or ERT over greater than or equal to 1.0 years in 02-N-0220/TKT/010/015 Study.

Patients who at least twice demonstrated significant improvement or normalization of sweat function (by QSART or thermoregulatory sweat test) or reduction in serum creatinine by at least 10% but return to the pre-infusion state before the subsequent biweekly enzyme infusion.

Patients who freely agree to participate in this study and understand the nature, risks and benefits of this study and give their written informed consent.

EXCLUSION CRITERIA:

Patients with Fabry disease, who are not already part of 00-N-0185/TKT011 or 02-N-0220/TKT015.

Patients on these protocols who have stable serum creatinine (or a lesser rise in serum creatinine than stipulated in the inclusion criteria), and do not show other objective evidence of incomplete clinical response between biweekly infusions (e.g. sweat function).

Patients who have begun dialysis or who have received a renal transplant.

Patients who cannot tolerate the study procedures or who are unable or unwilling to travel to the study center as required by this protocol.

Patients with an intercurrent medical condition that would render them unsuitable for mthe study e.g. HIV, diabetes. The reason is that the pathologies of these conditions will be significant confounders in assessing the effect of the experimental therapy and its adverse events.

Patients who in the opinion of the investigator (for whatever reason) are thought to be unsuitable for the study.

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00068107

Locations
United States, Maryland
National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland, United States, 20892
Sponsors and Collaborators
Baylor Research Institute
  More Information

Publications:
Responsible Party: Baylor Research Institute
ClinicalTrials.gov Identifier: NCT00068107     History of Changes
Other Study ID Numbers: 030286, 03-N-0286
Study First Received: September 6, 2003
Results First Received: March 12, 2015
Last Updated: March 19, 2015
Health Authority: United States: Food and Drug Administration

Keywords provided by Baylor Research Institute:
Lysosomal Storage
Renal Insufficiency
Stroke
Hypohidrosis
Peripheral Neuropathy
Fabry Disease

Additional relevant MeSH terms:
Fabry Disease
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Cardiovascular Diseases
Central Nervous System Diseases
Cerebral Small Vessel Diseases
Cerebrovascular Disorders
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Lipid Metabolism Disorders
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Metabolic Diseases
Nervous System Diseases
Vascular Diseases
Lipid Metabolism, Inborn Errors
Lipidoses
Metabolism, Inborn Errors
Sphingolipidoses

ClinicalTrials.gov processed this record on May 21, 2015