Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Tyvaso DPI is an inhaled dry powder formulation of treprostinil, a prostacyclin mimetic. It is indicated for the treatment of pulmonary arterial hypertension (PAH; WHO Group 1) and pulmonary hypertension associated with interstitial lung disease (PH-ILD; WHO Group 3), both to improve exercise ability. Treprostinil acts as a prostacyclin analogue, exerting its effects primarily through direct vasodilation of pulmonary and systemic arterial vascular beds and inhibition of platelet aggregation. The drug is administered via a handheld dry powder inhaler device, typically four times daily in single-breath doses per cartridge[2][5][7][9]. Tyvaso DPI was approved by the FDA in 2022 for these indications[7].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Tyvaso DPI.