Trials / Completed
CompletedNCT00376168
A Phase III Trial to Assess the Safety and Efficacy of Plant Cell Expressed GCD in Patients With Gaucher Disease
A Phase III, Multicenter, Randomized, Double-Blind Trial to Assess the Safety and Efficacy of Two Parallel Dose Groups of Plant Cell Expressed Recombinant Human Glucocerebrosidase (prGCD) in Patients With Gaucher Disease
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 32 (actual)
- Sponsor
- Pfizer · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Gaucher disease, the most prevalent lysosomal storage disorder, is caused by mutations in the human glucocerebrosidase gene (GCD) leading to reduced activity of the lysosomal enzyme glucocerebrosidase and thereby to the accumulation of substrate glucocerebroside (GlcCer) in the cells of the monocyte-macrophage system. This is the second trial to utilize a recombinant active form of lysosomal enzyme, glucocerebrosidase, (human prGCD) which is expressed and purified in a bioreactor system from transformed carrot plant root cell line.
Detailed description
This will be a multi-center, randomized, double-blind, parallel group, dose-ranging trial to assess the safety and efficacy of prGCD in 30 untreated patients with Gaucher disease. Patients will receive IV infusion of prGCD every two weeks at the selected medical center. The duration of the study will be nine months. At the end of the 9-month treatment period (20 visits, 38 weeks) eligible patients will be offered enrollment in an open-label extension study. There will be two treatment groups, 15 patients in each treatment group. Treatment Group I: 30 units/kg every 2 weeks. Treatment Group II: 60 units/kg every 2 weeks. All patients will have pharmacokinetic data collected over approximately 3 hours with frequent blood samples following the first and final doses of prGCD.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Plant cell expressed recombinant glucocerebrosidase (prGCD) | Intravenous infusion every two weeks for 9 months |
| DRUG | Plant cell expressed recombinant glucocerebrosidase (prGCD) | Intravenous infusion every 2 weeks for 9 months |
Timeline
- Start date
- 2007-08-01
- Primary completion
- 2009-09-01
- Completion
- 2009-10-01
- First posted
- 2006-09-14
- Last updated
- 2018-10-04
- Results posted
- 2012-07-26
Locations
11 sites across 8 countries: United States, Canada, Chile, Israel, Italy, South Africa, Spain, United Kingdom
Source: ClinicalTrials.gov record NCT00376168. Inclusion in this directory is not an endorsement.