Status:
COMPLETED
Safety and Pharmacokinetics of Recombinant Factor XIII in Healthy Volunteers
Lead Sponsor:
Novo Nordisk A/S
Conditions:
Congenital Bleeding Disorder
Congenital FXIII Deficiency
Eligibility:
All Genders
18-65 years
Phase:
PHASE1
Brief Summary
This trial was conducted in Europe. The aim of this trial was to investigate safety and pharmacokinetics of escalating single doses of catridecacog (recombinant factor XIII, rFXIII) in healthy volunte...
Eligibility Criteria
Inclusion
- Normal platelet count and clotting parameters
- Adequate renal and hepatic function
- If female and of child-bearing potential, negative serum pregnancy test within 21 days of enrollment and a negative urine pregnancy test on admission to the clinical research unit
- If a sexually active male or a sexually active female of child-bearing potential,agreement to use a medically accepted form of contraception from the time of enrollment to completion of all follow-up study visits
- Negative drug and alcohol screens
Exclusion
- Known antibodies or hypersensitivity to FXIII
- Known bleeding or hematologic disorder
- Known allergy to yeast
- Receipt of blood products within 30 days of screening
- Donation of blood within 30 days prior to enrollment
- Any surgical procedure in the 30 days prior to enrollment
- Previous history of autoimmune disorders involving autoantibodies, e.g., systemic lupus erythematosus
- Receipt of treatment with any experimental agent within 30 days of study enrollment
Key Trial Info
Start Date :
January 1 2003
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2003
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT01847989
Start Date
January 1 2003
End Date
May 1 2003
Last Update
January 11 2017
Active Locations (1)
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1
Novo Nordisk Investigational Site
Berkshire, United Kingdom, SL1 2 AD