Skip to content

CellCept 250 Special Drug Use Surveillance, Lupus nephritis

CellCept 250 Special Drug Use Surveillance, Lupus nephritis - CellCept 250 Special Drug Use Surveillance, Lupus nephritis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000027397
Enrollment
550
Registered
2017-06-05
Start date
2017-06-26
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

Lupus nephritis

Interventions

None listed

Sponsors

Chugai Pharmaceutical Co. Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The naive patients for Celcept,after diagnosed as SLE and LN on the basis of the ACR's criterion

Exclusion criteria

Exclusion criteria: Not applicable

Design outcomes

Primary

MeasureTime frame
Adverse reaction incidence Rate of achieving for the treatment by evaluation items eGFR, 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