Status:
COMPLETED
Safety of Recombinant Factor XIII (rFXIII) in Healthy Japanese Volunteers
Lead Sponsor:
Novo Nordisk A/S
Conditions:
Acquired Bleeding Disorder
Cardiac Surgery Requiring Cardiopulmonary Bypass
Eligibility:
MALE
20-65 years
Phase:
PHASE1
Brief Summary
This trial is conducted in Japan. The aim of this trial is to investigate the safety profile of recombinant factor XIII (rFXIII) assessed by the occurrence of adverse events in healthy Japanese subjec...
Eligibility Criteria
Inclusion
- Good general health based on assessment of medical history, physical examination, ECG (electrocardiogram) and clinical laboratory data at screening, as judged by the physician
- Body mass index (BMI) between 18.0-27.0 kg/m2 (both inclusive)
Exclusion
- The receipt of any investigational products for coagulation factor protein within 6 months prior to trial start (screening)
- Known or suspected allergy to yeast
- Known bleeding or hematologic disorder
- Significant history of alcoholism or drug/chemical abuse as judged by the physician or positive result in the alcohol breath test/screen of drugs at the trial start (screening)
- Smoking more than 10 cigarettes/day or equivalent
- Not able or willing to refrain from smoking whenever required for the trial procedures
- Habitual excessive consumption of methylxanthine-containing beverages and foods (coffee, tea, soft drinks such as cola, chocolate) as judged by the physician
- Excessive consumption of a diet deviating from a normal diet as judged by the physician
- Strenuous exercise as judged by the physician within 4 days prior to trial start (screening)
- Surgery or trauma with significant blood loss (500 mL or more blood) within 3 months prior to trial start (screening)
- Males who are sexually active and not surgically sterilised, who or whose partner are not using adequate contraceptive methods. Adequate contraceptive measures include that the subject uses a condom during intercourse or that the partner practices adequate conception (sterilisation, hormonal intrauterine devices and oral contraceptives).
Key Trial Info
Start Date :
June 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2010
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT01153997
Start Date
June 1 2010
End Date
August 1 2010
Last Update
June 18 2014
Active Locations (1)
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1
Fukuoka, Japan, 812-0025