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Cablivi Injection 10mg Drug Use Investigation for patients with aTTP

Cablivi Injection 10mg Drug Use Investigation for patients with aTTP - Cablivi Injection 10mg Drug Use Investigation for patients with aTTP

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000049385
Enrollment
120
Registered
2022-11-01
Start date
2022-12-23
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acquired thrombotic thrombocytopenic purpura

Interventions

None listed

Sponsors

Sanofi K.K.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients treated with Cablivi

Exclusion criteria

Exclusion criteria: NA

Design outcomes

Primary

MeasureTime 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

Sanofi_Medical@sanofi.com03-6301-3867

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026