IgA Nephropathy News and Research

RSS
IgA nephropathy (IgAN), also known as Berger’s disease, is the leading cause of primary glomerulonephritis all over the world. It is autoimmune in origin, characterized by the stimulation of genetically determined formation of concentration of IgA1 with galactose-deficient O-glycans in the hinge-region (Hit 1) in the blood. These stimulate anti-glycan antibody production, followed by binding with the aberrantly glycated IgA1.
Scientists identify genetic clues to chronic kidney disease

Scientists identify genetic clues to chronic kidney disease

Researchers uncover new genetic clues linked to autoimmune kidney disease

Researchers uncover new genetic clues linked to autoimmune kidney disease

Researchers discover strong genetic risk factor for IgA nephropathy

Researchers discover strong genetic risk factor for IgA nephropathy

Study links alpha-defensin genes to IgA nephropathy risk

Study links alpha-defensin genes to IgA nephropathy risk

NEFIGAN Trial of Nefecon for treatment of primary IgA nephropathy meets primary endpoint

NEFIGAN Trial of Nefecon for treatment of primary IgA nephropathy meets primary endpoint

Pharmalink AB acquires anti-inflammatory drug candidate from Synartro AB

Pharmalink AB acquires anti-inflammatory drug candidate from Synartro AB

Anthera Pharmaceuticals reports net loss of $7.0 million for third quarter 2014

Anthera Pharmaceuticals reports net loss of $7.0 million for third quarter 2014

Rigel Pharmaceuticals reports net loss of $20.9 million for third quarter of 2014

Rigel Pharmaceuticals reports net loss of $20.9 million for third quarter of 2014

Phase 2 study: Rigel's R348 fails to meet endpoints in patients with dry eye disease

Phase 2 study: Rigel's R348 fails to meet endpoints in patients with dry eye disease

Pharmalink’s core patents for Nefecon issued in United States, Europe, China and Hong Kong

Pharmalink’s core patents for Nefecon issued in United States, Europe, China and Hong Kong

Pharmalink's Busulipo receives FDA orphan drug designation

Pharmalink's Busulipo receives FDA orphan drug designation

Pharmalink commences Nefecon Phase IIb study in primary IgA nephropathy

Pharmalink commences Nefecon Phase IIb study in primary IgA nephropathy

Absence of proteinuria good prognostic sign in IgA nephropathy

Absence of proteinuria good prognostic sign in IgA nephropathy

Long-term prognosis excellent for patients with IgA nephropathy

Long-term prognosis excellent for patients with IgA nephropathy

Serum autoantibodies predict IgA nephropathy disease progression

Serum autoantibodies predict IgA nephropathy disease progression

Increasing blood levels of particular proteins may act as warning signs for IgA nephropathy

Increasing blood levels of particular proteins may act as warning signs for IgA nephropathy

Pharmalink raises SEK 35 million to further advance Nefecon and Busulipo

Pharmalink raises SEK 35 million to further advance Nefecon and Busulipo

New research on link between APOL1 gene variants and kidney disease in African Americans

New research on link between APOL1 gene variants and kidney disease in African Americans

Scientists identify biological pathways that mediate IgA nephropathy

Scientists identify biological pathways that mediate IgA nephropathy

Pharmalink's Nefecon for IgA nephropathy receives FDA orphan drug designation

Pharmalink's Nefecon for IgA nephropathy receives FDA orphan drug designation

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.