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  1. pharmadog
  2. ›drugs
  3. ›Vanrafia
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atrasentan hydrochloride

Marketedupdated 3mo ago
by $NVS NOVARTIS AG
Approved
community read0 votes

🐶 often sniffed alongside

top 3
  • drugVANRAFIA8 co-mentions · 2 sources
  • tagApproval8 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.

all catalysts(2)

approval · 2
Apr 2, 2025
approval
$NVS156.24-2.54%
1y ago
VANRAFIA (ATRASENTAN HYDROCHLORIDE) — FDA approval
atrasentan hydrochloride
→
Oct 20, 2025
approval
$NVS156.24-2.54%
10mo ago
VANRAFIA (ATRASENTAN HYDROCHLORIDE) — FDA approval
atrasentan hydrochloride
→

Patent cliff

source: FDA Orange Book
first barrier falls
Aug 22, 2028
~2.0 years out

Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.

patents (10)

  • Mar 25, 2043method-of-use (U-3980)US 12582631
  • Feb 23, 2041method-of-use (U-3980)US 12521369
  • Dec 16, 2040method-of-use (U-3980)US 11491137
  • Dec 16, 2040method-of-use (U-3980)US 11998526
  • Dec 16, 2040method-of-use (U-3980)US 12121509
  • Dec 16, 2040method-of-use (U-3980)US 12370174
  • Jul 7, 2034formulationUS 10016393
  • Jul 7, 2034formulationUS 9364458
  • Feb 18, 2032method-of-use (U-3980)US 11874283
  • Aug 22, 2028method-of-use (U-3980)US 86238192.0y

FDA exclusivities (1)

  • Apr 2, 2030NCENew Chemical Entity (5y)3.6y

News(1)

  • 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 · 2d 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
IgA Nephropathy (Berger's Disease)
phase
marketed
Data sources
openFDA · ClinicalTrials.gov
last refreshed 1h ago
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