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Actemra, Long-Term Special Drug Use Surveillance in Takayasu arteritis and Giant cell arteritis patients

Actemra, Long-Term Special Drug Use Surveillance in Takayasu arteritis and Giant cell arteritis patients - Actemra, Long-Term Special Drug Use Surveillance in TAK/GCA patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000029056
Enrollment
240
Registered
2017-09-13
Start date
2017-09-19
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

Takayasu arteritis, Giant cell arteritis

Interventions

None listed

Sponsors

Chugai Pharmaceutical Co. Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who have no medical history of Actemra SC and IV for TAK or GCA for the last 6 months.

Exclusion criteria

Exclusion criteria: No criteria

Design outcomes

Primary

MeasureTime frame
Incidence of adverse events and adverse drug reactions Daily fluctuation of corticosteroid Changes in clinical features of TAK/GCA Rate of relapse, etc.

Countries

Japan

Contacts

Public ContactAyaka Shimizu

Chugai Pharmaceutical Co. Ltd. Real World Data Science Dept.

shimizuayk@chugai-pharm.co.jp03-3273-0905

Outcome results

None listed

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