Voclosporin History and Updates

76 events · 2005 – present

Synced daily from openFDA and ClinicalTrials.gov. Last sync: .

3
FDA Approvals
0
Label Revisions
70
Trial Milestones
3
Pivotal Publications
Voclosporin — history and updatesFDA approvals, label revisions, recalls, trials, and pivotal publicationsFDA approvalsLabel revisionsRecalls + safetyTrialsPublications20062007200820092010201120122013201420152016201720182019202020212022202320242025202620272028202920302031Trial: NCT07053891 2025-09-17 → 2031-06-30 (primary completion)Trial: NCT07225387 2024-10-01 → 2027-01-31 (primary completion)Trial: NCT05962788 2024-03-28 → 2025-07-04 (primary completion)Trial: NCT06406205 2023-12-25 → 2027-06-30 (primary completion)Trial: NCT05288855 2023-10-10 → 2025-07-03 (primary completion)Trial: NCT05306873 2022-11-30 → 2024-06-13 (primary completion)Trial: NCT05337124 2022-04-05 → 2025-01-31 (primary completion)Trial: NCT05306379 2022-01-24 → 2022-04-05 (primary completion)Trial: NCT04701528 2020-11-15 → 2022-03-25 (primary completion)Trial: NCT04147650 2019-10-14 → 2020-09-17 (primary completion)Trial: NCT03597464 2019-09-29 → 2021-10-07 (primary completion)Trial: NCT03597139 2018-08-13 → 2018-11-09 (primary completion)Trial: NCT03598036 2018-06-21 → 2020-05-19 (primary completion)Trial: NCT03021499 2017-05-17 → 2019-09-24 (primary completion)Trial: NCT02949999 2016-10-31 → 2016-12-31 (primary completion)Trial: NCT02949973 2015-06-30 → 2016-12-31 (primary completion)Trial: NCT02141672 2014-06-30 → 2016-07-31 (primary completion)Trial: NCT01586845 2013-03-31 → 2015-12-31 (primary completion)FDA approval — 2021-01-22 FDA approved Lupkynis (voclosporin) (NDA 213716) Sponsor: AURINIA. Class: Type 1 - New Molecular Entity.FDA approval (supplemental) — 2024-04-29 FDA approved supplemental application for Lupkynis (voclosporin) — Efficacy (NDA 213716 S-4) Sponsor: AURINIA. Class: Efficacy.FDA approval (supplemental) — 2025-10-08 FDA approved supplemental application for Lupkynis (voclosporin) — Labeling (NDA 213716 S-8) Sponsor: AURINIA. Class: Labeling.Results posted — 2013-02-12 Trial results posted: NCT00270634 Study of ISA247 (Voclosporin) in De Novo Renal TransplantationResults posted — 2021-03-19 Trial results posted: NCT02949973 Aurinia Early Urinary Protein Reduction Predicts ResponseResults posted — 2021-05-18 Trial results posted: NCT02141672 AURA-LV: Aurinia Urinary Protein Reduction Active - Lupus With Voclosporin (AURA-LV)Results posted — 2021-06-16 Trial results posted: NCT03021499 Aurinia Renal Response in Active Lupus With VoclosporinResults posted — 2021-07-08 Trial results posted: NCT03597139 Ocular Tolerability of Voclosporin Ophthalmic Solution Versus Restasis® in Subjects With Dry Eye DiseaseResults posted — 2021-09-16 Trial results posted: NCT03598036 Dose-Exploration Evaluating the Efficacy and Safety of Voclosporin in Subjects With Focal Segmental GlomerulosclerosisResults posted — 2021-12-10 Trial results posted: NCT04147650 Dose Ranging Study to Assess the Efficacy and Safety of Voclosporin Ophthalmic Solution in Subjects With Dry Eye SyndromeResults posted — 2022-12-14 Trial results posted: NCT03597464 Aurinia Renal Assessments 2: Aurinia Renal Response in Lupus With VoclosporinResults posted — 2023-03-27 Trial results posted: NCT00244842 Randomized Placebo-controlled Study of ISA247 in Plaque PsoriasisResults posted — 2025-09-09 Trial results posted: NCT05306873 Examining Distinct Immunophenotypes to Validate and Enhance Rational Treatment in Systemic LupusPivotal publication — 2008-01-01 Efficacy of ISA247 in plaque psoriasis: a randomised, multicentre, double-blind, placebo-controlled phase III study. (Lancet) SPIRIT — Randomized Placebo-controlled Study of ISA247 in Plaque PsoriasisPivotal publication — 2011-01-01 Mycophenolate versus azathioprine as maintenance therapy for lupus nephritis. (N Engl J Med) AURORA — Aurinia Renal Response in Active Lupus With VoclosporinPivotal publication — 2022-01-01 Efficacy and safety of voclosporin versus placebo for lupus nephritis (AURORA 1): a double-blind, randomised, multicentre, placebo-controlled, phase 3 trial. (Lancet) AURORA — Aurinia Renal Response in Active Lupus With Voclosporintoday (2026-06-01)FDA approvalLabel revisionRecall or safetyTrial activityPivotal publication

Source: openFDA, ClinicalTrials.gov via AACT, PubMed · Hipa.ai, 2026-06-01Download chart as PNG

This page tracks every FDA action, clinical trial milestone, and major publication for Voclosporin since 2005, drawn from openFDA, ClinicalTrials.gov, and PubMed.

All published updates (6)

Upcoming & expected milestones

Primary completion· ClinicalTrials.gov
Safety and Efficacy of Combination Belimumab and Voclosporin in the Treatment of Proliferative Forms of Lupus Glomerulopathy: Synergy Trial
Primary completion· ClinicalTrials.gov
PRESERVE: LUPKYNIS in Combination With Belimumab, Obinutuzumab or Anifrolumab in Patients With Lupus Nephritis

Past events

2026
2025
Results posted· ClinicalTrials.gov
Examining Distinct Immunophenotypes to Validate and Enhance Rational Treatment in Systemic Lupus
Primary completion· ClinicalTrials.gov
A Prospective Observational Registry of Patients Treated With LUPKYNIS® (Voclosporin) in the US
2024
Trial started· ClinicalTrials.gov
Safety and Efficacy of Combination Belimumab and Voclosporin in the Treatment of Proliferative Forms of Lupus Glomerulopathy: Synergy Trial
2023
Trial started· ClinicalTrials.gov
A Study of QLG1074 Combined With Background Therapy in Subjects With Active Lupus Nephritis
2022
Trial started· ClinicalTrials.gov
Examining Distinct Immunophenotypes to Validate and Enhance Rational Treatment in Systemic Lupus
Trial started· ClinicalTrials.gov
A Prospective Observational Registry of Patients Treated With LUPKYNIS® (Voclosporin) in the US
Trial started· ClinicalTrials.gov
Drug-Drug Interaction Study to Investigate Effects of Voclosporin on Pharmacokinetics of Simvastatin
2021
Results posted· ClinicalTrials.gov
Dose Ranging Study to Assess the Efficacy and Safety of Voclosporin Ophthalmic Solution in Subjects With Dry Eye Syndrome
Results posted· ClinicalTrials.gov
Dose-Exploration Evaluating the Efficacy and Safety of Voclosporin in Subjects With Focal Segmental Glomerulosclerosis
Results posted· ClinicalTrials.gov
Ocular Tolerability of Voclosporin Ophthalmic Solution Versus Restasis® in Subjects With Dry Eye Disease
2020
Primary completion· ClinicalTrials.gov
Dose-Exploration Evaluating the Efficacy and Safety of Voclosporin in Subjects With Focal Segmental Glomerulosclerosis
2019
2018
Trial started· ClinicalTrials.gov
Ocular Tolerability of Voclosporin Ophthalmic Solution Versus Restasis® in Subjects With Dry Eye Disease
Trial started· ClinicalTrials.gov
Dose-Exploration Evaluating the Efficacy and Safety of Voclosporin in Subjects With Focal Segmental Glomerulosclerosis
2017
2016
2015
2014
2013
2012
2011
2010
2009
Primary completion· ClinicalTrials.gov
A Dose-Escalation Study to Assess the Safety and Tolerability of LX214 Ophthalmic Solution in Healthy Volunteers, Followed by an Open-Label
2008
2005

Sources

FDA approvals, label revisions, and recalls come from the public openFDA APIs (Drugs@FDA, Drug Label, Drug Enforcement). Drug-safety communications come from the FDA RSS feed. Trial milestones come from ClinicalTrials.gov via the AACT pg dump. Pivotal-publication events come from PubMed, filtered to high-impact journals linked to a Phase 3 trial in our inventory.