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United Therapeutics (UTHR)

Health Care · Rare disease / pulmonary hypertension pharmaceuticals

United Therapeutics is a rare disease specialist dominating pulmonary hypertension treatment through multiple treprostinil delivery formats while pursuing organ manufacturing innovation as a public benefit corporation.

What United Therapeutics does

United Therapeutics develops and commercializes therapies for serious rare diseases with unmet medical needs, with a primary focus on pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with interstitial lung disease (PH-ILD). The company's revenue is dominated by treprostinil-based therapies available in multiple delivery formats—including inhalation powder (Tyvaso DPI), nebulized inhalation solution (Nebulized Tyvaso), subcutaneous/intravenous injection (Remodulin), and oral tablets (Orenitram)—along with the phosphodiesterase-5 inhibitor Adcirca. The company also markets Unituxin, a monoclonal antibody for high-risk neuroblastoma, and operates as a public benefit corporation with a stated mission to advance organ manufacturing technologies alongside pharmaceutical innovation.

Themes: ["Pulmonary arterial hypertension (PAH) treatment","Pulmonary hypertension associated with interstitial lung disease (PH-ILD)","Treprostinil and prostacyclin pathway therapies","Rare disease / orphan drugs","Oncology (neuroblastoma immunotherapy)","Organ transplantation and regenerative medicine","Multiple delivery mechanisms for pulmonary drugs"]

Fundamentals

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Key risks (from latest filing)

["Heavy revenue concentration in treprostinil-based therapies; a material decrease in sales or prescribing patterns for Tyvaso DPI, Nebulized Tyvaso, Remodulin, or Orenitram would significantly harm operations","Generic competition and patent expiration risk; generic versions of treprostinil products have already negatively impacted revenues and additional generics could further erode market share","Clinical trial and regulatory approval uncertainty; failure to demonstrate safety and efficacy in development programs or delays in FDA approval could prevent commercialization of new products or indications and materially increase development costs"]

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Fundamentals: Finnhub, as of 2026-07-09. Filings: SEC EDGAR. Prices are delayed daily-close data.

Last updated 2026-07-09.

Informational only — NOT financial advice. All figures are delayed daily-close data from SEC EDGAR & Finnhub, shown with their as-of date.