Aurinia Sinks After FDA Official Questions Its Drug in Post (2)

Sept. 30, 2025, 11:18 AM UTC

Aurinia Pharmaceuticals Inc. slumped Monday after a top Food and Drug Administration official wrote and then deleted a post saying the company’s approved medicine for an immune disorder has “significant toxicity” and hasn’t been shown to help patients.

In a LinkedIn post that was subsequently removed, George Tidmarsh criticized the FDA’s 2021 approval of voclosporin, which is marketed under the name Lupkynis and used to treat lupus nephritis, a disorder that causes the body’s immune system to damage the kidneys. Tidmarsh later clarified that his earlier post reflected “my own personal views” and not those of the agency.

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