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LUPKYNIS Drug-use Results Survey

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Otsuka

Status

Enrolling

Conditions

Lupus Nephritis

Treatments

Drug: Voclosporin (LUPKYNIS)

Study type

Observational

Funder types

Industry

Identifiers

NCT07053891
348-101-00044

Details and patient eligibility

About

The purpose of this study is to survey the safety of LUPKYNIS in patients with lupus nephritis under actual use conditions. In addition, information on efficacy will be collected.

Enrollment

400 estimated patients

Sex

All

Ages

15+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who are newly starting administration of LUPKYNIS for lupus nephritis

Exclusion criteria

-

Trial contacts and locations

1

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Central trial contact

Pharmacovigilance Department Otsuka Pharmaceutical Co., Ltd

Data sourced from clinicaltrials.gov

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