SILVER SPRING, Md. & RESEARCH TRIANGLE PARK, N.C.--(BUSINESS WIRE)--United Therapeutics Corporation (Nasdaq: UTHR), a public benefit corporation, today announced record financial results for the quarter ended September 30, 2025, driven by continued year-over-year revenue growth in key products such as Tyvaso® and Orenitram®. Total revenues in the third quarter of 2025 grew seven percent year-over-year to $799.5 million, compared to $748.9 million in the third quarter of 2024. "Our commercial an. ...

Core Insights - Liquidia Corporation reported a second-quarter loss of 49 cents, which was worse than the consensus estimate of a loss of 43 cents, but sales reached $8.84 million, significantly exceeding the consensus of $3.86 million [1][2] Financial Performance - The company experienced a second-quarter loss of 49 cents per share, missing the expected loss of 43 cents [1] - Sales for the quarter were reported at $8.84 million, surpassing the consensus estimate of $3.86 million [1] Product Development and Market Response - Liquidia analyzed interim data from the ASCENT study, which involved 54 patients with pulmonary hypertension associated with interstitial lung disease (PH-ILD) [2] - The FDA approved and launched YUTREPIA™ (treprostinil) inhalation powder, with over 350 physicians prescribing it within 11 weeks of approval, leading to more than 900 unique patient prescriptions and over 550 patient starts [3] Analyst Ratings and Price Targets - Wells Fargo analyst Tiago Fauth maintained an Overweight rating on Liquidia and raised the price target from $25 to $31 [6] - Raymond James analyst Ryan Deschner maintained a Strong Buy rating and increased the price target from $33 to $41 [6]

Product & Approval - YUTREPIA (treprostinil) inhalation powder has received FDA approval [1,3] - YUTREPIA offers a new choice to treat PAH & PH-ILD [11] - The WAC price for a 28-day supply is $24,360, at parity with Tyvaso DPI® [23] Clinical Data & Dosing - YUTREPIA enables a wide range of dosing for both naïve and transition patients [16] - In the INSPIRE study, cough was observed in 27% of transitioning patients and 55% of naïve patients [17] - In the ASCENT study, the median dosing at Week 8 was 132.5 mcg [20] Market & Commercialization - The company is targeting 6,500 physicians treating PH, ILD, or both [27] - The commercial team is fully mobilized and will start detailing today [26] - The field force includes 60 commercial team members, 10 medical science liaisons, field reimbursement specialists, 140 specialty centers and 650 community accounts [27] Patient Support - The company offers full patient support services, including a voucher program, co-pay program, bridge program, and patient assistance program [24]