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YUTREPIA™ (treprostinil) inhalation powder

Pulmonary Arterial Hypertension (PAH)

ApprovedCommercialNCT03399604

Key Facts

Indication
Pulmonary Arterial Hypertension (PAH)
Phase
Approved
Status
Commercial
Company

About Liquidia

Liquidia's mission is to develop best-in-class therapies for rare cardiopulmonary diseases, helping patients breathe easier and live longer. The company has successfully transitioned from a technology platform to a commercial entity with the FDA approval and launch of YUTREPIA™ for pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with interstitial lung disease (PH-ILD). Its strategy centers on maximizing the commercial potential of YUTREPIA™, advancing its pipeline through clinical development, and exploiting the versatility of its PRINT® platform for future inhaled therapeutics.

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About Liquidia

Liquidia's mission is to develop best-in-class therapies for rare cardiopulmonary diseases, helping patients breathe easier and live longer. The company has successfully transitioned from a technology platform to a commercial entity with the FDA approval and launch of YUTREPIA™ for pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with interstitial lung disease (PH-ILD). Its strategy centers on maximizing the commercial potential of YUTREPIA™, advancing its pipeline through clinical development, and exploiting the versatility of its PRINT® platform for future inhaled therapeutics.

View full company profile

Other Pulmonary Arterial Hypertension (PAH) Drugs

DrugCompanyPhase
LIQ861 (treprostinil) inhalation powderLiquidiaPhase 3
L606 (liposomal treprostinil) injectionLiquidiaPreclinical
NTP42ATXA TherapeuticsPhase 1