Study Evaluating rFIX; BeneFIX in Severe Hemophilia B
Primary Purpose
Hemophilia B
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
BeneFIX
Sponsored by
About this trial
This is an interventional treatment trial for Hemophilia B focused on measuring Hemophilia B
Eligibility Criteria
Inclusion Criteria: Severe hemophilia B Less than 5 years of age In the investigator's judgment, the patient and/or caregiver will be compliant to study procedures Exclusion Criteria: A currently detectable FIX inhibitor. A family history of inhibitors will not exclude the patient. Impaired liver function Impaired renal function
Sites / Locations
Outcomes
Primary Outcome Measures
To characterize the safety and efficacy of rFIX in children less than 6 years of age with severe hemophilia B in the setting of acute bleeding episodes, prophylaxis, and/or surgery.
Secondary Outcome Measures
To measure the incremental recovery of rFIX in children following a 75-IU/kg bolus infusion.
Full Information
NCT ID
NCT00037557
First Posted
May 17, 2002
Last Updated
December 18, 2007
Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
1. Study Identification
Unique Protocol Identification Number
NCT00037557
Brief Title
Study Evaluating rFIX; BeneFIX in Severe Hemophilia B
Official Title
An Open-Label, Single-Arm, Safety and Efficacy Study of Recombinant Human Factor IX (rFIX; BeneFIX®) in Children Less Than 6 Years of Age With Severe Hemophilia B
Study Type
Interventional
2. Study Status
Record Verification Date
December 2007
Overall Recruitment Status
Completed
Study Start Date
September 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
November 2007 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
4. Oversight
5. Study Description
Brief Summary
To characterize the safety and efficacy of rFIX in children less than 6 years of age with severe hemophilia B in the setting of acute bleeding episodes, prophylaxis, and/or surgery.
This study will provide an opportunity for systematic observation of treatment with rFIX in children less than 6 years of age regardless of prior FIX treatment. Younger patients exhibit a different pharmacokinetic profile and therefore may respond differently to rFIX infusions when compared with older children and adults. This evaluation will provide data from which recommendations can be made regarding rFIX dosing and treatment of these patients. Surveillance for certain observations that have been made in patients treated with rFIX in the clinical and postmarketing setting will be performed, including inhibitor development, thrombogenicity, FIX recovery/lack of effect, allergic-type manifestations, and RBC agglutination. Comparisons will be derived from published reports and communications describing experience with other FIX products and protein therapeutics in general.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemophilia B
Keywords
Hemophilia B
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
BeneFIX
Primary Outcome Measure Information:
Title
To characterize the safety and efficacy of rFIX in children less than 6 years of age with severe hemophilia B in the setting of acute bleeding episodes, prophylaxis, and/or surgery.
Secondary Outcome Measure Information:
Title
To measure the incremental recovery of rFIX in children following a 75-IU/kg bolus infusion.
10. Eligibility
Sex
All
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Severe hemophilia B
Less than 5 years of age
In the investigator's judgment, the patient and/or caregiver will be compliant to study procedures
Exclusion Criteria:
A currently detectable FIX inhibitor. A family history of inhibitors will not exclude the patient.
Impaired liver function
Impaired renal function
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Medical Monitor, MD
Organizational Affiliation
Wyeth is now a wholly owned subsidiary of Pfizer
Official's Role
Study Director
Facility Information:
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80262
Country
United States
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States
City
New Brunswick
State/Province
New Jersey
ZIP/Postal Code
08903
Country
United States
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599-7220
Country
United States
City
Dayton
State/Province
Ohio
ZIP/Postal Code
45404
Country
United States
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
26196195
Citation
Rendo P, Smith L, Lee HY, Shafer F. Nonacog alfa: an analysis of safety data from six prospective clinical studies in different patient populations with haemophilia B treated with different therapeutic modalities. Blood Coagul Fibrinolysis. 2015 Dec;26(8):912-8. doi: 10.1097/MBC.0000000000000359.
Results Reference
derived
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Study Evaluating rFIX; BeneFIX in Severe Hemophilia B
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