Liquidia Technologies Inc (NASDAQ:LQDA) saw its shares rise nearly 10% following news that it will begin its initial commercial shipments of YUTREPIA™ (treprostinil) inhalation powder. This milestone follows FDA approval granted on May 23, 2025, for the treatment of pulmonary arterial hypertension (PAH) and pulmonary hypertension linked to interstitial lung disease (PH-ILD). The product will soon be accessible to patients through specialty pharmacies.

The strong market reaction reflects Liquidia’s swift efforts to launch YUTREPIA, including rapid listing with major compendia and distribution to specialty pharmacies within just five business days post-approval. This quick rollout follows a favorable legal outcome, where the U.S. District Court for the Middle District of North Carolina rejected United Therapeutics’ (NASDAQ:UTHR) attempt to block Liquidia’s commercialization through a preliminary injunction and restraining order.

Liquidia CEO Dr. Roger Jeffs highlighted the company’s rapid execution, noting, “We have moved with exceptional speed to provide a new and differentiated therapeutic alternative to the marketplace. In just over one week, our sales force hit the ground running with the promotion of YUTREPIA, the product was listed with compendia, and commercial product was shipped to specialty pharmacies.”

The court’s decision significantly reduces legal uncertainty for Liquidia, as it found United Therapeutics unlikely to prevail on its patent infringement claims. This ruling paves the way for Liquidia to proceed with the full commercial launch of YUTREPIA.

Investor enthusiasm is buoyed by Liquidia’s ability to overcome regulatory and legal hurdles quickly, boosting confidence in YUTREPIA’s prospects as a leading treatment option for patients suffering from PAH and PH-ILD. The stock’s upward movement today highlights the importance of timely product launches and favorable legal outcomes in influencing market sentiment.

Liquidia Technologies stock price

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