Acquired thrombotic thrombocytopenic purpura
Conditions
Interventions
None listed
Sponsors
Sanofi K.K.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All patients treated with Cablivi
Exclusion criteria
Exclusion criteria: NA
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence during the observation period of adverse drug reaction mainly related to the safety specifications | — |
Countries
Japan
Contacts
Public ContactMasahiro Tamura
Medical Affairs Post-authorization regulatory studies
Outcome results
None listed