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United Therapeutics Advances in Pulmonary Fibrosis Treatment with Phase 3 Study

United Therapeutics Advances in Pulmonary Fibrosis Treatment with Phase 3 Study

United Therapeutics Corp. ((UTHR)) announced an update on their ongoing clinical study.

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United Therapeutics Corp. is conducting a Phase 3 clinical study titled A Randomized, Double-blind, Placebo-controlled, Multinational, Phase 3 Study of the Efficacy and Safety of Inhaled Treprostinil in Subjects With Progressive Pulmonary Fibrosis (TETON-PPF). The study aims to evaluate the safety and efficacy of inhaled treprostinil in patients with progressive pulmonary fibrosis over a 52-week period. This research is significant as it seeks to provide a new treatment option for a challenging condition.

The study tests inhaled treprostinil, delivered via an ultrasonic nebulizer, against a placebo. Treprostinil is intended to improve lung function and quality of life in patients with progressive pulmonary fibrosis by targeting pulmonary hypertension.

This interventional study is randomized and uses a parallel assignment model. It is quadruple-masked, meaning that the participant, care provider, investigator, and outcomes assessor are all blinded to the treatment allocation. The primary purpose of the study is treatment-focused.

The study began on October 30, 2023, with an estimated primary completion date in 2025. The last update was submitted on July 29, 2025. These dates are crucial as they indicate the study’s progress and when results might be expected.

For investors, this study could impact United Therapeutics’ stock performance, especially if the results are positive, as it may lead to a new marketable treatment. The competitive landscape includes other companies developing treatments for pulmonary fibrosis, which could influence investor sentiment.

The study is currently recruiting, and further details are available on the ClinicalTrials portal.

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