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Corporate Overview

Aurinia Pharmaceuticals Inc. is a biopharmaceutical company focused on delivering therapies to people living with autoimmune diseases with high unmet medical needs. In January 2021, the Company introduced LUPKYNIS (voclosporin), the first FDA-approved oral therapy for the treatment of adult patients with active lupus nephritis. Aurinia is also developing aritinercept, a dual inhibitor of B cell-activating factor (BAFF) and a proliferation-inducing ligand (APRIL) for the potential treatment of autoimmune diseases.

Download Corporate Presentation
Aurinia Corporate Presentation November 2025
Forward-Looking Statements This presentation contains forward-looking statements within the meaning of applicable U.S. securities law and forward-looking information within the meaning of applicable Canadian securities law.
Changing the Trajectory of Autoimmune Diseases
Recent Financial Results
Results for the Three Months Ended September 30
Results for the Nine Months Ended September 30
Cash Flows and Financial Position
2025 Financial Guidance
LUPKYNIS® – A calcineurin inhibitor (CNI) indicated in combination with a background immunosuppressive regimen for the treatment of adult patients with active lupus nephritis. The first oral therapy approved for the treatment of lupus nephritis
Lupus Nephritis (LN) Is Among the Most Severe and Dangerous Complications of Systematic Lupus Erythematosus (SLE)
Proteinuria Reduction Is Associated with Long-Term Renal Preservation
Recent American College of Rheumatology (ACR)Lupus Nephritis Treatment Guideline Update
LUPKYNIS Is a Novel, Structurally Modified CNI that Targets LN with a Dual Mechanism of Action
Robust Clinical Study History
Significantly More Patients on LUPKYNIS Achieved a Complete Renal Response in AURORA 1 as Early as Week 24
LUPKYNIS Rapidly Reduced Proteinuria in Fewer Days in AURORA 1
New Analysis Shows LUPKYNIS Associated with 53% Reduction in Risk of Renal-Related Event or Death
Adverse Reactions Occurring in ≥3% of Patients Treated with LUPKYNIS 23.7 mg Twice a Day and ≥2% Higher than Placebo in AURORA 1 and AURA-LV
Aritinercept – A dual BAFF/APRIL inhibitor for the potential treatment of autoimmune diseases
Aritinercept Is a Dual BAFF/APRIL Inhibitor
Role of BAFF and APRIL
Aritinercept Is a High Affinity Dual BAFF/APRIL Inhibitor
Aritinercept Potently Inhibits BAFF-and APRIL-Mediated B Cell Proliferation
Aritinercept Single Ascending Dose (SAD) Study: Design
Aritinercept SAD Study:Safety Summary
Aritinercept SAD Study: Single Doses of Aritinercept Led to Robust and Long-Lasting Reductions in Immunoglobulins in Humans
Effect of a Single Dose of BAFF/APRIL Inhibitors on IgA
Effect of a Single Dose of BAFF/APRIL Inhibitors on IgM
Effect of a Single Dose of BAFF/APRIL Inhibitors on IgG
Summary and Next Steps
Aurinia Pharmaceuticals Inc., 2025. All rights reserved.

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Stock Information

NASDAQ Global Market: AUPH

$15.64

+2.47

/

+18.75%

894K

Volume

Last update:
11/04/2025 9:44AM ET
Pricing delayed by 15 minutes

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Past Events

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May 31
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Jun 3, 2023
May 31, 2023 12:00 AM
2023

European Congress of Rheumatology, EULAR 2023

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May 17
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May 17, 2023
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2023 Annual General Meeting

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May 4, 2023
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First Quarter 2023 Financial Results Conference Call

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Apr 5
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Apr 5, 2023
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2023

Renal Biopsy Substudy Top-line Results Presentation Link

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Mar 14, 2023
Mar 14, 2023 9:20 AM
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2023

Oppenheimer 33rd Annual Virtual Healthcare Conference

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SEC Filings

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May 10, 2018
2018
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6-K
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Current report of foreign issuer pursuant to Rules 13a-16 and 15d-16 Amendments
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May 10, 2018
2018
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6-K
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Current report of foreign issuer pursuant to Rules 13a-16 and 15d-16 Amendments
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April 6, 2018
2018
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Voluntary supplemental material filed pursuant to Section 11(a) of the Securities Act of 1933 by foreign issuers
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March 29, 2018
2018
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Notice of Effectiveness
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March 26, 2018
2018
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Registration statement for securities of certain Canadian issuers under the Securities Act of 1933
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Position Description - President - CEO
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IR Contact

General inquiries can be sent to ir@auriniapharma.com