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United Therapeutics’ Tyvaso DPI Receives the US FDA’s Approval for Treatment of PAH and PH-ILD

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United Therapeutics’ Tyvaso DPI Receives the US FDA’s Approval for Treatment of PAH and PH-ILD

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  • The approval was based on the (BREEZE) open-label study evaluating Tyvaso DPI in 51 patients with PAH. Additionally, commercialization activities are currently underway with patient availability is expected in June 2022
  • The results from the patients with PAH who were transitioned from Tyvaso inhalation sol. to Tyvaso DPI demonstrated safety and tolerance @3wk. treatment period, improvements in six-minute walk distance, device preference and satisfaction & PROs
  • Tyvaso DPI marks the first US FDA approved dry powder inhaler therapy & is indicated for use in PAH and PH-ILD and represents a new formulation and inhalation device for inhaled treprostinil

Ref: Businesswire | Image: United Therapeutics

Click here to­ read the full press release 

Neha

Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

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