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Liquidia Corporation - LQDA STOCK NEWS

Welcome to our dedicated page for Liquidia Corporation news (Ticker: LQDA), a resource for investors and traders seeking the latest updates and insights on Liquidia Corporation stock.

Overview

Liquidia Corporation (LQDA) is a United States-based biopharmaceutical company dedicated to transforming therapy development for pulmonary hypertension and other rare cardiopulmonary diseases. Utilizing its proprietary PRINT® Technology, the company engineers precise, uniform drug particles to optimize drug delivery and improve treatment efficacy. This innovative approach addresses critical gaps in current therapeutic options, ensuring products are manufactured under scalable, cGMP-compliant processes.

Core Technology and Business Model

At its core, Liquidia harnesses the power of PRINT® Technology to overcome common challenges in drug delivery. By producing highly controlled and uniform particles, the company enhances deposition in the lungs, which is vital for conditions such as pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with interstitial lung disease (PH-ILD). Liquidia’s model includes both the advancement of its own pipeline and strategic licensing of its technology to globally recognized pharmaceutical partners.

Product Portfolio and Clinical Focus

Liquidia’s primary product candidate, YUTREPIA™ (treprostinil) inhalation powder, exemplifies its application of precision particle engineering for the treatment of PAH and PH-ILD. The company is also developing additional candidates and formulations, including a sustained-release liposomal version designed for twice-daily administration, further diversifying its clinical offerings. This broad clinical focus reinforces Liquidia’s commitment to addressing unmet patient needs.

Market Position and Competitive Landscape

Positioned in a competitive biopharmaceutical landscape, Liquidia distinguishes itself through its unique technological platform and rigorous adherence to quality standards. Its scalable PRINT® process, combined with robust clinical research and strategic partnerships, offers a scientifically sound alternative in a market with significant unmet needs. Industry-specific terms such as "drug particle engineering", "inhaled therapeutics", and "cGMP compliance" attest to the company’s technical expertise and operational rigor.

Operational Excellence and Regulatory Focus

Liquidia’s operations are streamlined across its specialized subsidiaries, ensuring efficient research, development, and commercialization processes. The company maintains a strict focus on quality by aligning its manufacturing practices with the highest regulatory standards, hence building a foundation of trust and reliability in its product offerings. This diligence in quality control and regulatory adherence solidifies its reputation within the oncology and pulmonary care communities.

Industry Collaboration and Strategic Partnerships

Liquidia actively collaborates with major pharmaceutical entities, both to license its PRINT® platform and to accelerate the commercialization of its products. These partnerships allow for a mutual exchange of expertise and resources, further enhancing its market reach and ensuring that advanced therapies are delivered efficiently. Such strategic alliances are critical for fostering innovation and establishing a competitive advantage in the complex healthcare landscape.

Commitment to Innovation and Quality

With a commitment to continuous innovation, Liquidia leverages extensive clinical studies and state-of-the-art manufacturing processes to bring safer and more effective treatment options to patients. Emphasizing precision in every phase of development, the company sets itself apart by ensuring that its therapies are optimally designed to tackle the challenges of pulmonary hypertension and related ailments.

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Liquidia (NASDAQ: LQDA) executives to provide business update at the 23rd Annual Needham Virtual Healthcare Conference on April 9, 2024.
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Liquidia (LQDA) announces legal victories clearing the path for YUTREPIA™ approval for PAH and PH-ILD treatment. United Therapeutics' legal actions and expired exclusivity for Tyvaso® impact the regulatory landscape.
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Liquidia Corporation (LQDA) reported financial results for 2023, preparing to launch YUTREPIA™ upon FDA approval. The Federal Circuit rejected United Therapeutics' request for rehearing on '793 Patent. The company aims to become a full-scale commercial entity in 2024. Financially, revenue increased to $17.5 million, but net loss rose to $78.5 million in 2023.
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Liquidia Corporation (LQDA) will report its full year 2023 financial results on March 13, 2024, with a webcast to discuss financial results and corporate updates.
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Liquidia Corporation (NASDAQ: LQDA) announced the presentation of data from the L606 clinical program at the Pulmonary Vascular Research Institute (PVRI) 2024 Annual Congress. L606 is an investigational, sustained-release formulation of treprostinil for treating patients with pulmonary arterial hypertension and pulmonary hypertension associated with interstitial lung disease. The presentation will take place on February 2, 2024, in London, England. The poster will be available on the Company’s website after the presentation.
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Liquidia Corporation announces FDA update on YUTREPIA NDA for treating pulmonary arterial hypertension and pulmonary hypertension associated with interstitial lung disease. The FDA is confirming the process for adding the PH-ILD indication as an amendment to the NDA for YUTREPIA, causing a delay in the action letter issuance. The FDA did not request additional clinical data and did not issue a new PDUFA goal date. The company remains committed to preparing for the final FDA approval of YUTREPIA. Litigation filed by United Therapeutics alleging patent infringement of U.S. Patent No. 10,716,793 and U.S. Patent No. 11,826,327 is ongoing.
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Liquidia Corporation announced updates to its operations leadership, with CFO Michael Kaseta taking on the role of COO as well. The company also promoted Michael Hunter to Senior Vice President of Manufacturing Operations, while former COO Robert Lippe will transition out of the company. These changes come in anticipation of the potential approval and launch of YUTREPIA™ (treprostinil) inhalation powder.
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Liquidia Corporation (LQDA) files counterclaims against United Therapeutics Corporation (UTHR) seeking dismissal of claims related to ‘793 patent and declaration that ‘327 patent is not infringed, invalid, and unenforceable in response to amended patent infringement complaint. Liquidia also asserts that UTHR failed to disclose prior art references and additional material information during prosecution of the ‘327 patent.
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Liquidia Corporation (LQDA) enrolled the first PH-ILD patient in the open-label ASCENT study for YUTREPIA and confirmed with the FDA that a single pivotal efficacy trial with L606 will support PAH and PH-ILD indications. The FDA has tentatively approved YUTREPIA for PH-ILD with a PDUFA goal date of January 24, 2024. Liquidia also reached an agreement with the FDA regarding the registration requirements for L606 using the 505(b)(2) regulatory pathway, requiring only a single Phase 3 placebo-controlled efficacy trial in PH-ILD patients to support indications for both PAH and PH-ILD. The company is preparing to initiate a global study for L606 in 2024 and continues to enroll patients in an ongoing open-label, multicenter safety study of L606 in U.S. patients with PAH or PH-ILD.
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Liquidia Corporation (LQDA) announced a $100 million capital raise through a private placement with Patient Square Capital and HealthCare Royalty, signaling confidence in the company's strategy and the value of its product YUTREPIA. The private placement of 7,182,532 shares of common stock at a purchase price of $10.442 per share is expected to yield gross proceeds of approximately $75.0 million. Additionally, an advance of $25.0 million was received from HealthCare Royalty under the current financing agreement. The company has now secured a total of $126 million in gross proceeds in the last month.
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FAQ

What is the current stock price of Liquidia Corporation (LQDA)?

The current stock price of Liquidia Corporation (LQDA) is $12.77 as of April 9, 2025.

What is the market cap of Liquidia Corporation (LQDA)?

The market cap of Liquidia Corporation (LQDA) is approximately 994.6M.

What is Liquidia Corporation's core business?

Liquidia Corporation develops innovative therapies for pulmonary hypertension and other rare cardiopulmonary diseases using its proprietary PRINT® Technology for precise drug particle engineering.

How does PRINT® Technology enhance drug delivery?

PRINT® Technology enables the scalable production of uniform drug particles, ensuring optimal deposition in the lungs and improved efficacy for inhaled therapeutics.

Which therapeutic areas does Liquidia focus on?

The company primarily focuses on pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with interstitial lung disease (PH-ILD), addressing significant unmet patient needs.

How does Liquidia generate revenue?

Liquidia generates revenue through the development of its own product candidates and by licensing its innovative PRINT® Technology to global pharmaceutical partners.

What differentiates Liquidia from its competitors?

Liquidia’s unique PRINT® Technology, enabling precise and scalable drug particle engineering, combined with its focus on quality and regulatory compliance, sets it apart in the biopharmaceutical sector.

How does Liquidia ensure the quality and safety of its products?

The company adheres to stringent cGMP-compliant processes and maintains robust regulatory oversight, ensuring that all products meet high quality and safety standards.

What role do strategic partnerships play in Liquidia’s business model?

Strategic partnerships allow Liquidia to leverage external expertise and resources, enhancing the development and commercialization of its innovative therapies and expanding its market reach.
Liquidia Corporation

Nasdaq:LQDA

LQDA Rankings

LQDA Stock Data

994.58M
71.19M
13.88%
61.4%
13.32%
Biotechnology
Pharmaceutical Preparations
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United States
MORRISVILLE