A Study Investigating Treatment Factor X in People With Factor X Deficiency
Status: | Completed |
---|---|
Conditions: | Hematology |
Therapuetic Areas: | Hematology |
Healthy: | No |
Age Range: | 12 - Any |
Updated: | 3/30/2013 |
Start Date: | January 2010 |
End Date: | August 2013 |
Contact: | Kate Gillanders, Mrs |
Email: | kate.gillanders@bpl.co.uk |
Phone: | +44 (0)208 957 2562 |
A Phase III Open, Multicentre Study to Investigate the Pharmacokinetics, Safety and Efficacy of BPL's High Purity Factor X in the Treatment of Severe and Moderate Factor X Deficiency.
The main objective of the study is to assess the pharmacokinetics of FACTOR X after a single
dose of 25IU/kg.
The secondary objectives of the study are to assess efficacy and safety of FACTOR X in the
treatment of bleeding episodes over at least 6 months.
Inclusion Criteria:
- Written informed consent given, or for subjects aged 12-17 years, have given written
assent and whose parent/guardian has given written informed consent
- At least 12 years of age at dtae of written informed consent
- Have hereditary severe or moderate FX deficiency
- Currently treated with Fresh Frozen Plasma FFP, Prothrombin Complex Concentrate PCC
or factor IX/X concentrate
- Must have a minimum of one spontaneous or menorrhagic bleed in the last 12 months
which required treatment of FFP, PCC or factor IX/X concentrate. Newly diagnosed
subjects who present at the hospital with a bleed may be included
- Must have had at least 7 days, and ideally 10-14 days, since an infusion of either
FFP, PCC or factor IX/X concentrate at Baseline Visit
- Females of child bearing potential must have a negative result on a HCG based
pregnancy test. If they are or become sexually active, they must practise
contraception by using a method of proven reliability for the duration of the study
Exclusion Criteria:
- Have a history of inhibitor development to FX or a positive result at the Screening
Visit
- Bleeding at the appointment for the PK assessment
- Subjects who have thrombocytopenia
- Have clinically significant liver disease
- Known to have other coagulopathy or thrombophilia
- Have known or suspected hypersensitivity to the investigational medicinal product or
its excipients
- Have abused chemicals or drugs within the past 12 months
- Have a history of unreliability or non-cooperation
- Participating or have taken part in another trial within the last 30 days, with the
exception of BPL FX surgery study - Protocol Ten03. In such cases, subjects should
have completed their End of Study Visit either before or on the day of Screening
Visit for this study
- Female subjects who are pregnant or lactating
- Subjects planning greater than 4 weeks absence from the locality of the
Investigational site, between the screening visit and the repeat PK assessment
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