TYVASO DPI IS NOW APPROVED

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For the treatment of pulmonary hypertension associated with interstitial lung disease (PH-ILD; WHO Group 3) to improve exercise ability.

FOR US HEALTHCARE PROFESSIONALS ONLY

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The first and only FDA-approved treatment for PH-ILD1

TYVASO SHIFTS
THE OUTLOOK FOR PH-ILD1

TYVASO and TYVASO DPI are inhaled prostacyclin mimetics indicated for the treatment of pulmonary hypertension associated with interstitial lung disease (PH-ILD; WHO Group 3) to improve exercise ability.1,2

The study with TYVASO establishing effectiveness predominately included patients with etiologies of1,2:

  • Idiopathic interstitial pneumonia (IIP) (45%) inclusive of idiopathic pulmonary fibrosis (IPF)
  • Combined pulmonary fibrosis and emphysema (CPFE) (25%)
  • WHO Group 3 connective tissue disease (22%)
Most eligible TYVASO patients who enroll may pay as little as a $0 co-pay per prescription

Eligible patients
could pay as little
as a $0 co-pay
for each prescription

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