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Liquidia

Liquidia is a biopharmaceutical company that develops, manufactures and commercializes products for rare cardiopulmonary diseases, built around its proprietary PRINT particle-engineering technology for uniform drug particles with controlled size and shape. Its lead product, Yutrepia, is an inhaled dry-powder formulation of treprostinil approved for pulmonary arterial hypertension and for pulmonary hypertension associated with interstitial lung disease, and the company promotes Remodulin, a treprostinil injection, under an agreement with Sandoz. A third program, L606, is an investigational liposomal, sustained-release inhaled treprostinil licensed from Pharmosa Biopharm in Phase 3 development for PAH and PH-ILD. Founded in 2004 and headquartered in Morrisville, North Carolina, Liquidia listed on Nasdaq in July 2018 and turned sharply profitable in 2026 on Yutrepia's commercial ramp — second-quarter 2026 revenue reached roughly $171.7 million with net income of about $74.7 million. The equity carries a concentrated legal tail: on September 30, 2026 a Delaware federal court held two claims of a United Therapeutics patent valid and infringed by Yutrepia in the PH-ILD indication, while invalidating the other four asserted claims; the company has said it will appeal and may remove the PH-ILD indication from the label, and sought remedies threaten product availability.

Company Info

Sector:Biopharmaceuticals / Cardiopulmonary
Headquarters:Morrisville, North Carolina, USA
Founded:2004

Upcoming Milestones & Key Dates

Q4 2026
Legal / Regulatory

Appeal of the September 30, 2026 Delaware district court ruling on the United Therapeutics PH-ILD patent; possible removal of the PH-ILD indication from the Yutrepia label

November 2026
Earnings

Third-quarter 2026 financial results

Clinical Development Pipeline

Yutrepia (treprostinil) inhalation powder

Target: Inhaled dry-powder treprostinil (PRINT-engineered particles)
Pulmonary arterial hypertension and pulmonary hypertension associated with interstitial lung disease
Preclinical
Phase 1
Phase 2
Phase 3
Approved

Remodulin (treprostinil) injection

Target: Continuous intravenous and subcutaneous treprostinil infusion (promoted under agreement with Sandoz)
Pulmonary arterial hypertension
Preclinical
Phase 1
Phase 2
Phase 3
Approved

L606

Target: Liposomal sustained-release inhaled treprostinil (licensed from Pharmosa Biopharm)
Pulmonary arterial hypertension and PH-ILD
Preclinical
Phase 1
Phase 2
Phase 3
Approved

Recent News

No recent news updates available for this company.

Leadership Team

Dr. Roger A. Jeffs, PhD

Chief Executive Officer and Director

Michael Kaseta

Chief Operating Officer and Chief Financial Officer

Dr. Rajeev Saggar, MD

Chief Medical Officer

Careers & Job Openings

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Multiple Departments
Morrisville, North Carolina, USA
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