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FDA approves Gazyva/Gazyvaro (obinutuzumab) for the treatment of lupus nephritis – Roche

Written by | 1 Nov 2025

Roche announced  that the FDA  has approved Gazyva/Gazyvaro (obinutuzumab) for the treatment of adult patients with active lupus nephritis (LN) who are receiving standard therapy, as well as… read more.

New AURORA 1 analysis: Lupkynis-based triple immunosuppressive therapy yields deep proteinuria reduction in lupus nephritis – Aurinia Pharma

Written by | 5 Jul 2025

Aurinia Pharmaceuticals Inc.  announced that a post-hoc analysis of the 52-week, Phase III AURORA 1 study presented at at LUPUS 2025, the 16th International Congress on SLE, showed… read more.

Safety and efficacy profile of Lupkynis (voclosporin) for people with lupus nephritis presented at European Alliance of Associations for Rheumatology Congress – Aurinia Pharma

Written by | 25 Jun 2024

Aurinia Pharmaceuticals Inc. announced an oral presentation at the European Alliance of Associations for Rheumatology (EULA R) 2024 taking place in Vienna, Austria June 12-15. The data reinforces… read more.

FDA approves updated Lupkynis (voclosporin) label to include long term data from the Aurora Clinical Program – Aurinia Pharmaceuticals

Written by | 7 May 2024

Aurinia Pharmaceuticals Inc. announced that the FDA has approved a label update for Lupkynis. The updated label no longer includes language indicating that the safety and efficacy of… read more.

Long term phase III data published in Arthritis & Rheumatology shows Lupkynis preserved kidney function up to three years in lupus nephritis patients with no new or unexpected adverse events – Aurinia Pharma

Written by | 28 Jul 2023

Aurinia Pharmaceuticals Inc. announced that full results from the Phase III, double-blind, placebo-controlled AURORA 2 extension study were published online in Arthritis & Rheumatology, the official peer-reviewed journal… read more.

Early diagnosis and monitoring of lupus nephritis — on your smartphone

Written by | 7 Feb 2023

A team of researchers at the University of Houston is reporting the success of their new method for the early diagnosis and monitoring of lupus nephritis — at… read more.

European Commission approves Benlysta for adult patients with active lupus nephritis – GSK

Written by | 13 May 2021

GlaxoSmithKline plc announced the European Commission has approved the expanded use of intravenous and subcutaneous Benlysta (belimumab) in combination with background immunosuppressive therapies for the treatment of adult… read more.

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