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Terminated Phase 2 Interventional

Study of Efficacy and Safety of LNP023 in Participants With Active Lupus Nephritis Class III-IV, +/- V

ClinicalTrials.gov ID: NCT05268289

Public ClinicalTrials.gov record NCT05268289. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 10:27 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Adaptive, Randomized, Double-blind, Dose Exploration, Parallel Group, Placebo Controlled, Multicenter Phase 2 Trial to Evaluate the Efficacy, Safety and Tolerability of LNP023 in Combination With Standard-of-care With and Without Oral Corticosteroids in Patients With Active Lupus Nephritis Class III-IV, +/- V

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The overall purpose of this two-part study is to evaluate the efficacy, safety and tolerability of iptacopan (LNP023) in addition to standard of care treatment.

Study identification

NCT ID
NCT05268289
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
81 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 100 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 10, 2022 (Actual)
Primary completion
Mar 19, 2026 (Actual)
Completion
Oct 1, 2026 (Actual)
Last update posted
Oct 15, 2026

2022 – 2026

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
16
Facility City State ZIP Site status
Ronald Reagan UCLA Medical Center Los Angeles California 90095 —
Loma Linda University San Bernardino California 92408 —
Olive View UCLA Medical Center Sylmar California 91342 —
University of Colorado Denver Aurora Colorado 80045 —
Royal Research Corp Hollywood Florida 33021 —
Nephrology Associates Of Central FL Orlando Florida 32806 —
Florida Kidney Physicians Riverview Florida 33578 —
Nep Assoc of Northern Illinois Hinsdale Illinois 60521 —
Wichita Community Clcl Onco Program Wichita Kansas 67214 —
Ochsner Health System New Orleans Louisiana 70121 —
Johns Hopkins Hospital Baltimore Maryland 21287 —
Stony Brook Internists PC East Setauket New York 11733 —
Cleveland Clinic Foundation Cleveland Ohio 44195 —
Temple University Philadelphia Pennsylvania 19140 —
Dallas Nephrology Associates Dallas Texas 75204 —
Prolato Clinical Research Center Houston Texas 77054 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 58 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05268289, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 15, 2026 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05268289 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →