United Therapeutics and Miromatrix Medical announce completion of tender offer and merger
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United Therapeutics Corporation History
Please see Important Safety Information for our FDA approved products under the Research and Medicine tab.
2023
United Therapeutics acquires IVIVA Medical Inc.
2022
First successful xenotransplantation of porcine heart
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Tyvaso DPI® (treprostinil) inhalation powder approved by the FDA for the treatment of PAH and PH-ILD to improve exercise capacity
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United Therapeutics Corporation Annual Report
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2021
INCREASE results published in New England Journal of Medicine
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Commercial launch of the Remunity® Pump for Remodulin®
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FDA approval and launch of Tyvaso® for the treatment of PH-ILD
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UT becomes a public benefit corporation
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United Therapeutics Corporation Annual Report
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2020
FDA clearance of pharmacy fill Remunity® Pump for Remodulin®
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UT issues first Corporate Responsibility Report
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INCREASE study of Tyvaso® in PH-ILD meets primary endpoint
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UT launches TETON study in IPF
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United Therapeutics Corporation Annual Report
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2019
UT in-licenses Ralinepag an oral, IP receptor agonist being developed for PAH
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Orenitram® label expansion and relaunch
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United Therapeutics Corporation Annual Report
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2018
FREEDOM-EV study of Orenitram® meets primary endpoint
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UT launches collaboration with MannKind for Tyvaso DPI®
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Health Canada approves Unituxin®
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United Therapeutics Corporation Annual Report
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2017
UT's subsidiary, Lung Biotechnology PBC, launches organ bioprinting program in collaboration with 3D Systems
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FDA approves TD-300 Nebulizer for Tyvaso®
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United Therapeutics Corporation Annual Report
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2016
Launch of Unither 2.0, Major Pipeline Expansion
UT obtains $1 billion unsecured line of credit
United Therapeutics Corporation Annual Report
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2015
Unituxin® approved by FDA to treat high-risk neuroblastoma
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UT enters into collaboration with Mayo Clinic to build and operate an ex-vivo lung perfusion center in Jacksonville, Florida
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United Therapeutics Corporation Annual Report
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2014
Japanese regulators approve Remodulin® for PAH under the brand name Treprost™
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First ex-vivo lung perfusion procedure performed by Lung Bioengineering, a subsidiary of UT
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UT opens Regenerative Medicine Lab in Research Triangle Park, North Carolina, with a focus on manufacturing lungs and lung lobes for transplant
UT and DEKA Research & Development Corp. enter into an agreement to develop a next-generation subcutaneous pump for Remodulin®, which ultimately resulted in the Remunity® Pump for Remodulin®
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United Therapeutics Corporation Annual Report
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2013
Orenitram® approved by FDA for the treatment of PAH to improve exercise capacity
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UT annual revenues surpass $1 billion
United Therapeutics Corporation Annual Report
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2011
FREEDOM-M study of Orenitram® meets primary endpoint
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Intravenous Remodulin® approved in most of E.U.
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Adcirca® becomes most prescribed drug for PAH
United Therapeutics acquires Revivicor xenotransplantation program
United Therapeutics Corporation Annual Report
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Annual Report Soundtrack
01 – “Dear Shareholders” performed by the Alan Scott Band
02 – “Live it up” performed by the Alan Scott Band
03 – “2011” performed by the Alan Scott Band
04 – “Helicopter” performed by the Alan Scott Band
2010
United Therapeutics launches collaboration with National Cancer Institute to develop a monoclonal antibody for treatment of high-risk neuroblastoma, which is today known as Unituxin®
United Therapeutics Corporation Annual Report
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2009
UT surpasses $1 billion in assets
Adcirca® approved by FDA for the treatment of PAH to improve exercise capacity
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Tyvaso® approved by FDA for the treatment of PAH to improve exercise capacity
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United Therapeutics Corporation Annual Report
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2008
UT in-licenses U.S. commercialization rights to Adcirca® for PAH from Eli Lilly and Company
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United Therapeutics Corporation Annual Report
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2007
TRIUMPH-1 study of inhaled treprostinil meets primary endpoint
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United Therapeutics Corporation Annual Report
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2006
FDA approves expansion of Remodulin® label to include transitions from Flolan®
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United Therapeutics Corporation Annual Report
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2005
Remodulin®® approved by 23 countries in the European Union for the treatment of PAH to improve exercise capacity by subcutaneous infusion
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United Therapeutics Corporation Annual Report
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2004
FDA approves expansion of Remodulin® label to include treatment of PAH by intravenous infusion
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United Therapeutics Corporation Annual Report
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2003
UT commences first human clinical trial of an oral formulation of treprostinil
United Therapeutics Corporation Annual Report
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2002
Remodulin® approved in the United States, Canada and Israel to treat PAH by subcutaneous infusion
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United Therapeutics Corporation Annual Report
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2001
United Therapeutics Corporation Annual Report
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2000
UT submits new drug application to FDA for Remodulin® to treat pulmonary arterial hypertension
1999
United Therapeutics acquires rights to treprostinil from Glaxo Wellcome Inc.
United Therapeutics acquires Synquest, Inc., providing in-house capacity and expertise to manufacture treprostinil
1997
Initial public offering (Nasdaq:UTHR), priced at $12.00 per share
1996
United Therapeutics founded by Martine Rothblatt to find a cure for her daughter's life- threatening condition, now known as pulmonary arterial hypertension