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General Drug Use-results Survey of Rituxan Intravenous Infusion - Systemic Sclerosis -

General Drug Use-results Survey of Rituxan Intravenous Infusion - Systemic Sclerosis -

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT2031210659
Enrollment
400
Registered
2022-03-10
Start date
2022-03-10
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

Systemic sclerosis

Interventions

None listed

Sponsors

Ando Takashi
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with systemic sclerosis who have received Rituxan intravenous infusion.

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
Incidence of adverse events and adverse drug reactions. Clinical global Impression - improvement, patient global Impression - improvement.

Contacts

Public ContactJunko Sakamoto

Zenyaku Kogyo, Co., LTD.

Junko_Sakamoto@mail.zenyaku.co.jp+81-3-3946-1136

Outcome results

None listed

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