A Study of Safety and Effectiveness of NovoThirteen® (rFXIII) During Treatment of Congenital FXIII Deficiency in Japan
- Conditions
- Congenital Bleeding DisorderCongenital FXIII Deficiency
- Interventions
- Registration Number
- NCT02670213
- Lead Sponsor
- Novo Nordisk A/S
- Brief Summary
This study is conducted in Asia. Tha aim of this study is to investigate Safety and Effectiveness of NovoThirteen® (rFXIII) during treatment of congenital FXIII deficiency in Japan.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ENROLLING_BY_INVITATION
- Sex
- All
- Target Recruitment
- 8
Inclusion Criteria
- Male of female patients, regardless of age, requiring treatment with NovoThirteenR for whom the treating physician has decided to use NovoThirteenR (rFXIII) treatment
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Exclusion Criteria
Not provided
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Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description NovoThirteen® recombinant factor XIII -
- Primary Outcome Measures
Name Time Method Adverse drug reactions in patients with congenital FXIII A-subunit deficiency treated with NovoThirteen®, comprising FXIII antibodies, allergic reactions, embolic and thrombotic events and lack of therapeutic effect Year 0-9
- Secondary Outcome Measures
Name Time Method All technical complaints Year 0-9 Frequency of bleeding episodes Year 0-9 All serious adverse events Year 0-9 All adverse events Year 0-9 All medical event of special interest Year 0-9 All medication errors collected Year 0-9 Use of NovoThirteen® for other uses than for the approved indication Year 0-9
Trial Locations
- Locations (1)
Novo Nordisk Investigational Site
🇯🇵Tokyo, Japan