Reports Q1 revenue $2.97M, consensus $4.39M. Cash and cash equivalents totaled $157.9M as of March 31, compared to $83.7M as of December 31, 2023. Roger Jeffs, Liquidia’s CEO, said: “We continue to vigorously pursue final agency action for YUTREPIA’s approval for pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with interstitial lung disease (PH-ILD). And as we have shown, we will remain relentless in the defense of our freedom to go to market despite the myriad of legal filings by our competitor. At our core is our steadfast commitment to deliver YUTREPIA to patients with PAH and PH-ILD. We feel YUTREPIA can provide an important and differentiated alternative to address lingering unmet needs that continue to limit the optimal delivery of inhaled treprostinil.”
Published first on TheFly – the ultimate source for real-time, market-moving breaking financial news. Try Now>>
Read More on LQDA:
- Liquidia Corporation Reports First Quarter 2024 Financial Results and Provides Corporate Update
- Is LQDA a Buy, Before Earnings?
- Liquidia announces presentation on open-label safety study of L606 at ATS 2024
- Liquidia Announces Poster Presentation at the American Thoracic Society (ATS) 2024 International Conference on Its Open-Label Safety Study of L606 (Liposomal Treprostinil) in Patients with PAH and PH-ILD
- Liquidia Corporation to Present at 23rd Annual Needham Virtual Healthcare Conference