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  1. pharmadog
  2. ›drugs
  3. ›VANRAFIA
drug · small molecule
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VANRAFIA

updated 5mo ago
by $NVS NOVARTIS AG🔗 ChEMBL
community read0 votes

🐶 often sniffed alongside

top 3
  • tagApproval8 co-mentions · 2 sources
  • drugatrasentan hydrochloride8 co-mentions · 2 sources
  • tagSmall Molecule4 co-mentions · 2 sources

Small molecule drug with a maximum clinical stage of Phase 3 (across all indications), with 3 investigational indications.

targets

Endothelin-1 receptor

all catalysts(0)

nothing on the calendar yet

News(2)

  • Novartis shareholder calls for board overhaul following costly deal setbacks: Reuters
    Novartis’ recent dual clinical setbacks have prompted questions from a major shareholder about the board’s oversight of dealmaking.
    fiercebiotech · 20d ago
  • STAT+: Pharmalittle: We’re reading about a setback for Eyepoint, a win for Amylyx, and more
    Eyepoint disclosed that a Phase 3 trial of its experimental treatment for a common cause of age-related blindness fell short of its primary goal
    stat · 1mo ago
brand
VANRAFIA
generic
ATRASENTAN HYDROCHLORIDE
MOA
12.1 Mechanism of Action Atrasentan is an ET A receptor antagonist (Ki = 0.034 nM) with >1800-fold selectivity for the ET A receptor compared to the endothelin type B receptor (Ki = 63.3 nM). Endothelin (ET)-1 is thought to contribute to the pathogenesis of IgAN via the ET A R.
indication
1 INDICATIONS AND USAGE VANRAFIA 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. This indication is approved under accelerated approval based on a reduction of proteinuria [see Clinical Studies (14.1)] . It has not been established whether VANRAFIA slows kidney function decline in patients with IgAN. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory clinical trial. VANRAFIA is an endothelin receptor antagonist 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. ( 1 ) This indication is approved under accelerated approval based on a reduction of proteinuria. It has not been established whether VANRAFIA slows kidney function decline in patients with IgAN. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory clinical trial. ( 1 )
Data sources
ClinicalTrials.gov · OpenTargets
last refreshed 5h ago
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