Features and properties of sparsentan
Alternative names | DEARA; FILSPARI; PS-433540; RE-021 |
Class | Anti-inflammatories; antihypertensives; isoxazoles; nerve growth factors; small molecules; spiro compounds; sulfonamides; urologics; vascular disorder therapies |
Mechanism of action | Angiotensin II type 1 receptor antagonists; endothelin type A receptor antagonists |
Route of administration | Oral |
Pharmacodynamics | Shows nephroprotective effects in rodent models of IgA nephropathy and focal segmental glomerulosclerosis |
Pharmacokinetics | Less than dose-proportional, time-dependent pharmacokinetics; time to peak plasma concentration ≈ 3 h; volume of distribution 61.4 L; apparent clearance 5.11 L/h; half-life 9.6 h |
Most frequent adverse events | Peripheral oedema, hypotension (including orthostatic hypotension), dizziness, hyperkalaemia, anaemia |
ATC codes | |
WHO ATC code | G04B-X (Other Urologicals) |
EphMRA ATC code | G4X (All Other Urological Products) |
Chemical name | 4′-((2-butyl-4-oxo-1,3-diazaspiro[4.4]non-1-en-3-yl)methyl)-N-(4,5-dimethylisoxazol-3-yl)-2'-(ethoxymethyl)-[1,1'-biphenyl]-2-sulfonamide |