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Dual Acting Receptor Antagonist drug approvalDual Acting Receptor Antagonist drug approvalDual Acting Receptor Antagonist drug approvalDual Acting Receptor Antagonist drug approval
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  • Reagents
    • Biochemical Targets
      • Autophagy
      • Bioactive Lipids
      • Cellular Metabolism
      • Cellular trafficking
      • Cytoskeleton
      • DNA Damage/Repair
      • Epigenetics
      • Gene regulation
      • GPCRs
      • Ions and other channels
      • Kinases
      • Mitochondria
      • Nuclear receptors
      • Transcription factors
      • Ubiquitin/Proteasome
      • View All
    • Physiological Processes
      • Bioprocessing
      • Cancer
      • Cardiovascular
      • Cell Cycle
      • Cellular Senescence
      • Cellular Stress
      • Circadian clock
      • Diabetes
      • Immunology
      • Inflammation
      • Neurodegeneration
      • Obesity and metabolic diseases
      • Pain
      • Programmed Cell Death
      • Stem cells
      • View All
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Sildenafil and Neurodegeneration
April 16, 2026
AMPK a target for Hepatocellular carcinoma
April 17, 2026

Dual Acting Receptor Antagonist drug approval

Published by Focus Biomolecules on April 16, 2026

FOCUS on New Drug Approvals. On April 13th the FDA approved Travere Therapeutics’ Sparsentan (Filspari) as the first approved treatment for reduction of proteinuria in adult and pediatric patients with focal segmental glomerulosclerosis (FSGS). FSGS is a rare kidney disease characterized by scarring. Sparsentan is a DARA (Dual Acting Receptor Antagonist) acting as an endothelin A and angiotensin II receptor antagonist. It was previously approved for reducing proteinuria in immunoglobulin A nephropathy.

FOCUS Biomolecules can supply Sparsentan for research applications. Contact us for more information.

Focus Biomolecules • Plymouth Meeting, PA USA • 1-855-FOCUS21

Focus Biomolecules
Plymouth Meeting, PA USA
1-855-FOCUS21

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