LUPKYNIS Drug-use Results Survey

Recruiting

• Conditions: Lupus Nephritis

• Registration Number: NCT07053891
• Lead Sponsor: Otsuka Pharmaceutical Co., Ltd.

Brief Summary

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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2025-06-27
• Study First Submitted QC: 2025-06-27
• Status Verified: 2025-07
• Study Start: 2025-07-01
• Last Update Submitted: 2025-07-07
• Study First Posted: 2025-07-08
• Last Update Posted: 2025-07-10
• Primary Completion: 2031-06-30
• Study Completion: 2032-06-30

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 400

Inclusion Criteria

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

Exclusion Criteria

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Safety Information (Number of Adverse Event)	3 years from the initiation of LUPKYNIS treatment	Any untoward medicinal occurrence in a patient or clinical study subject administered a Medicinal Product and which does not necessarily have a causal relationship with this treatment (ICH-E2A Guideline). An Adverse Event can therefore be any unfavorable and unintended sign (e.g. abnormal laboratory finding), symptom, or disease temporally associated with the use of a Medicinal Product (LUPKYNIS), whether or not it is considered causally related to the Medicinal Product.
Safety Information (Types of Special Situations and the Number of Corresponding Cases)	3 years from the initiation of LUPKYNIS treatment	Situations related to the use of an Otsuka product which may or may not be associated with an adverse event: * Maternal (pregnancy and breastfeeding) or paternal (via semen) exposure; * Exposure during breastfeeding; * Overdose/Incorrect dosage, misuse, abuse (e.g. patient sharing products); -Medication errors (e.g. patient took wrong dose); * Lack of therapeutic efficacy (e.g. the product doesn't work); * Occupational exposure (e.g.: nurse administering the product is exposed); * Cases of suspected transmission of infectious agents; * Use of suspected or confirmed falsified product(s) or quality defect of the product(s); * Withdrawal reactions; -Accidental exposure (e.g.: child takes parent's product); * Drug-drug/drug-food interactions; * Unintentional use of product in a non-approved population (e.g.: pediatric or geriatric population); * Disease progression/exacerbation of existing disease.
Safety Information (Number of off-Label Use)	3 years from the initiation of LUPKYNIS treatment	Collecting any type of off-Label Use that refers to situations where a product is intentionally used for a medical purpose not in accordance with the authorized product information. Off-label use also includes the intentional use in non-authorized population categories not indicated in the label.
Safety Information (Number of Serious Adverse Event)	3 years from the initiation of LUPKYNIS treatment	Any adverse drug experience/event occurring at any dose which; * results in death; * is life-threatening; * requires inpatient hospitalization or prolonged of existing hospitalization; * results in persistent or significant disability or incapacity; * is a congenital anomaly/birth defect; * is medically significant.
Safety Information (Number of Non-serious Adverse Events)	3 years from the initiation of LUPKYNIS treatment	All Adverse Events that do not meet the definition of a serious Adverse Event are considered non-serious Adverse Events.

Trial Locations

Locations (1)

Pharmacovigilance Department; 🇯🇵 Osaka, Japan