Sparsentan

Generic Name
Sparsentan
Brand Names
Filspari
Drug Type
Small Molecule
Chemical Formula
C32H40N4O5S
CAS Number
254740-64-2
Unique Ingredient Identifier
9242RO5URM
Background

Sparsentan is a dual antagonist of the endothelin type A receptor (ETR) and the angiotensin II (Ang II) type 1 receptor (ATR) with a similar affinity for both (9.3 nM for ETR and 0.8 nM for ATR). Sparsentan is first in its class and orally active, and was created by merging the structural elements of irbesartan, an ATR antagonist, and biphenylsulfonamide, an...

Indication

Sparsentan is indicated to reduce proteinuria in adults with primary immunoglobulin A nephropathy (IgAN) at risk of rapid disease progression, generally a urine protein-to-creatinine ratio (UPCR) ≥1.5 g/g.

Associated Conditions
Proteinuria
Associated Therapies
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defenseworld.net
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BNP Paribas Financial Markets Sells 1,586 Shares of Ligand Pharmaceuticals Incorporated

BNP Paribas Financial Markets reduced its stake in Ligand Pharmaceuticals by 27.6% during Q3. Several investors modified their holdings, with Woodstock Corp, Creative Planning, and Mirae Asset Global Investments increasing their positions. Insiders sold shares worth $2.27 million in the last quarter. LGND stock opened at $116.91, with a consensus rating of 'Buy' and an average target price of $145.33. Ligand Pharmaceuticals develops and licenses biopharmaceutical assets globally.

Japan MHLW grants orphan drug status to Renalys' sparsentan for IgAN treatment

The Japanese Ministry of Health, Labour, and Welfare has granted orphan drug designation to Renalys Pharma’s sparsentan for primary IgA nephropathy. Sparsentan, developed by Travere Therapeutics, received FDA approval in September and is being advanced by Renalys Pharma in Japan and Asia. The therapy aims to address kidney function decline in IgA nephropathy, a leading cause of kidney failure in Japan.
hcplive.com
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FDA Clears Initiation of Phase 2 Efficacy Trial for Ruxoprubart in IgAN

The FDA has approved a Phase 2 trial for ruxoprubart, an anti-Bb monoclonal antibody targeting the alternative pathway for treating Immunoglobulin A nephropathy (IgAN). Ruxoprubart, developed by NovelMed, aims to improve clinical outcomes for IgAN patients, affecting 82,000-110,000 individuals in the US. The drug's selective pathway inhibition differentiates it from other complement blockers, potentially treating various renal disorders. NovelMed seeks strategic partners to advance ruxoprubart to Phase 2/3 trials.
firstwordpharma.com
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Sparsentan receives Orphan Drug Designation for primary IgA nephropathy in Japan

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biospace.com
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10 Promising IgA Nephropathy Drugs in Line to Get Approval

IgA nephropathy affects 25-50 per million annually, with 20–40% progressing to end-stage kidney disease. Diagnosed cases in the US are expected to reach 135,000 by 2030. Treatments include ACE inhibitors, ARBs, corticosteroids, and immunosuppressants. FDA-approved treatments are TARPEYO, FILSPARI, and FABHALTA. The IgA nephropathy market is projected to reach ~USD 4.1 billion by 2034, driven by novel therapies like Novartis’ Atrasentan, Otsuka/Visterra’s Sibeprenlimab, Vertex/Alpine’s Povetacicept, and others.
quantisnow.com
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Travere Therapeutics Presents Data Reinforcing Clinical Benefit of FILSPARI® (Sparsentan)

Travere Therapeutics presented new data on FILSPARI (sparsentan) at ASN Kidney Week 2024, showing its effectiveness in IgA nephropathy (IgAN) and focal segmental glomerulosclerosis (FSGS). Key findings include rapid and sustained proteinuria reduction, significant complete remission rates in IgAN patients, and safety in combination therapies. The data also highlighted long-term kidney health benefits in genetic, treatment-resistant FSGS patients.
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