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A Study of Safety and Effectiveness of NovoThirteen® (rFXIII) During Treatment of Congenital FXIII Deficiency in Japan

Conditions
Congenital Bleeding Disorder
Congenital 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
GroupInterventionDescription
NovoThirteen®recombinant factor XIII-
Primary Outcome Measures
NameTimeMethod
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 effectYear 0-9
Secondary Outcome Measures
NameTimeMethod
All technical complaintsYear 0-9
Frequency of bleeding episodesYear 0-9
All serious adverse eventsYear 0-9
All adverse eventsYear 0-9
All medical event of special interestYear 0-9
All medication errors collectedYear 0-9
Use of NovoThirteen® for other uses than for the approved indicationYear 0-9

Trial Locations

Locations (1)

Novo Nordisk Investigational Site

🇯🇵

Tokyo, Japan

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