Factor VIIa, Recombinant |
NovoSeven |
Clinical Trial: Study to Establish Bioequivalence of ReFacto AF (BDDrFVIII) with Advate (FLrFVIII) in Hemophilia A
This study is currently recruiting patients.
Verified by Wyeth August 2005
|
Purpose
| Condition | Intervention | Phase |
|---|---|---|
| Hemophilia A | Gene Transfer: ReFacto AF Gene Transfer: B-Domain deleted Recombinant Factor VIII Gene Transfer: BDDrFVIII | Phase III |
MedlinePlus related topics: Hemophilia
Study Type: Interventional
Study Design: Prevention, Randomized, Double-Blind, Active Control, Crossover Assignment, Safety/Efficacy Study
Official Title: A Randomized Two-Way Blinded Crossover-Design Study to Establish the Bioequivalence of B-Domain Deleted Recombinant Factor VIII (BDDrFVIII,Refacto AF) with a Full Length Recombinant Factor VIII Preparation (FLrFVIII,Advate), Followed by an Open-Label Trial of the Safety and Efficacy of ReFacto AF in Previously Treated Patients with Hemophilia A.
Secondary Outcomes: To characterize the efficacy of ReFActo AF in preventing and treating bleeding episodes during prophylaxis.To characterize PK of ReFacto AF as compared to Advate over time.
Expected Total Enrollment: 100
Study start: July 2005
Eligibility
Inclusion Criteria:
- Male subjects with severe or moderately severe hemophilia A
- A negative past medical history of a Factor VIII inhibitor
- Age greater than or equal to 12 years
Exclusion Criteria:
- A history of Factor VIII inhibitors
- Presence of a bleeding disorder in addition to hemophilia
- Known hypersensitivity to hampster protein
Location and Contact Information
Australia
Perth, 6000, Australia; Not yet recruiting
Belgium
Leuven, 3000, Belgium; Not yet recruiting
Finland
Helsinki, 00029, Finland; Not yet recruiting
France
Le Kremlin Bicêtre, 94275, France; Not yet recruiting
Rouen, 76031, France; Not yet recruiting
Germany
Muenster, 48143, Germany; Not yet recruiting
Berlin, 10249, Germany; Not yet recruiting
Hungary
Budapest, H-1135, Hungary; Recruiting
Italy
Milano, 20122, Italy; Not yet recruiting
Netherlands
Groningen, Netherlands; Not yet recruiting
New Zealand
Auckland, New Zealand; Not yet recruiting
Hamilton, New Zealand; Not yet recruiting
Poland
Lodz, 95-510, Poland; Not yet recruiting
Poznan, Poland; Not yet recruiting
Wroclaw, Poland; Not yet recruiting
Warszawa, 00-576, Poland; Not yet recruiting
Spain
Valencia, 46009, Spain; Not yet recruiting
Madrid, 28046, Spain; Not yet recruiting
Sweden
Malmö, Sweden; Not yet recruiting
Stockholm, 171 76, Sweden; Not yet recruiting
Medical Monitor, Study Director, Wyeth Research
Trial Manager, Principal Investigator, For Australia, China, Hong Kong, New Zealand, South Korea and Taiwan, medinfo@wyeth.com
Trial Manager, Principal Investigator, For Nordic Area, Norway and Sweden, MedInfoNord@wyeth.com
Trial Manager, Principal Investigator, For Poland and Ukraine, med-info-poland@wyeth.com
Trial Manager, Principal Investigator, All other countries, contact clinicaltrialinfo@wyeth.com and we will send you the appropriate contact information.
More Information
Last Updated: August 31, 2005
Record first received: August 30, 2005
ClinicalTrials.gov Identifier: NCT00141843
Health Authority: United States: Food and Drug Administration; Belgium: Institutional Review Board; France: Ministry of Health; Germany: Ethics Commission; Italy: Ministry of Health; Mali: Ministry of Health; Bulgaria: Bulgarian Drug Agency; Greece: National Organization of Medicines; Turkey: Ministry of Health; Spain: Ministry of Health; Portugal: National Pharmacy and Medicines Institute; United Arab Emirates: Drug Control Department - Medicines and Pharmacy Control - Ministry of Health; United Arab Emirates: Drug Control Department - Medicines and Pharmacy Control - Ministry of Health; Switzerland: Swissmedic; Israel: Israeli Health Ministry Pharmaceutical Administration; Hungary: National Institute of Pharmacy; Croatia: Ministry of Health and Social Care; Poland: Ministry of Health; Czech Republic: State Institute for Drug Control; United Kingdom: National Health Service; Australia: Human Research Ethics Committee; New Zealand: Health Research Council; Taiwan: Department of Health
ClinicalTrials.gov processed this record on 2005-09-06
Resources
- Factor VIIa, Recombinant (Drug Digest)
- NovoSeven (Drug Digest)

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