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Windtree Therapeutics Announces Engagement of Strategic Advisor to Support Assessment of Strategic Alternatives

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Windtree Therapeutics, Inc. has engaged Ladenburg Thalmann & Co. Inc. to evaluate strategic alternatives with the goal of maximizing stockholder value. The company has made significant progress in advancing its cardiovascular portfolio, including clinical trials in cardiogenic shock and a licensing deal with Lee’s Pharmaceuticals for the Greater China-Asia Pacific region. Windtree is actively exploring strategic alternatives such as acquisition, merger, further licensing, or company sale to maximize shareholder value.
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The engagement of a strategic advisor by Windtree Therapeutics to explore strategic alternatives is a significant move aimed at enhancing shareholder value. This decision typically indicates that a company is looking for ways to improve its financial position, either through partnerships, mergers, acquisitions, or even a sale. The mention of a non-dilutive licensing deal and the elimination of a substantial contingent liability are positive indicators of a proactive management team working to strengthen the company's financial standing.

From a financial perspective, the potential expansion of the clinical development program and the improvement of the balance sheet could make Windtree more attractive to potential partners or buyers. The company's focus on late-stage interventions for critical cardiovascular disorders, a market with high unmet medical needs, presents opportunities for growth. However, investors should be aware that such processes are uncertain and can take considerable time, with no guarantee of a favorable outcome.

Windtree's emphasis on advancing its cardiovascular portfolio, particularly istaroxime for cardiogenic shock, is noteworthy. Cardiogenic shock is a condition with high mortality rates and limited treatment options, making successful interventions highly valuable. The clinical progress and the licensing agreement for the Asia-Pacific region suggest that the company is making strides in both product development and market expansion.

The engagement of Ladenburg Thalmann & Co. Inc. to evaluate strategic alternatives could be a strategic move to leverage the company's clinical advancements and to explore opportunities that could accelerate the development and commercialization of its therapies. It is important for stakeholders to monitor the outcomes of these strategic discussions, as they could have a significant impact on the company's future and the accessibility of its treatments.

Windtree's perception of being under-recognized and undervalued by the financial markets is an issue that many biotechnology firms face, particularly those in the late-stage development phase without a commercial product. The biotech industry is known for its high volatility and risk and companies like Windtree must consistently communicate their value proposition to investors.

Engaging a strategic advisor indicates that Windtree is actively seeking to correct this undervaluation by exploring various strategic alternatives. For investors, this could represent a pivotal point in the company's trajectory. The outcomes of these strategic discussions could lead to significant changes in the company's market valuation and should be closely watched for developments that may alter the investment landscape for Windtree Therapeutics.

WARRINGTON, Pa., Jan. 31, 2024 (GLOBE NEWSWIRE) -- Windtree Therapeutics, Inc. (“Windtree” or the “Company”) (NasdaqCM: WINT), a biotechnology company focused on advancing late-stage interventions for critical cardiovascular disorders, today announced that it has engaged Ladenburg Thalmann & Co. Inc. (“Ladenburg”) to evaluate strategic alternatives for the Company with the goal of maximizing stockholder value.

“We are pleased with the progress we have made in advancing our cardiovascular portfolio, most importantly progressing istaroxime in clinical trials in cardiogenic shock, as well as the recently announced licensing deal with Lee’s Pharmaceuticals for the Greater China-Asia Pacific region. We believe this non-dilutive licensing deal along with significantly cutting cash burn and the agreement for the elimination of the $15 million contingent liability with Deerfield has resulted in both a potentially expanded clinical development program and a stronger balance sheet,” said Craig Fraser, Windtree's President and Chief Executive Officer. “While there has been positive data and progress, we believe the opportunity is under-recognized and under-valued in the current financial markets, however, it has resulted in in-bound business development interest. Given this, the Company has engaged a strategic advisor to help coordinate and assess these opportunities with the intent to maximize shareholder value.”

Windtree is making this announcement to inform shareholders and the public that in addition to the active execution of the next steps in our cardiogenic shock program outlined in our corporate deck and filings, the Company is also engaging in discussions for strategic alternatives with the goal of maximizing value for stockholders. Beyond traditional licensing, the Company will explore the potential for an acquisition, merger, further licensing, company sale or other strategic transactions. There can be no assurances that the process or discussions will result in an attractive transaction, nor as to its outcome or timing and the Company has not made any decisions at this point in time. The engagement of Ladenburg as strategic advisor is intended to support the board’s process and assessment of opportunities.

About Istaroxime
Istaroxime is a first-in-class dual-mechanism therapy designed to improve both systolic and diastolic cardiac function. Istaroxime is a positive inotropic agent that increases myocardial contractility through inhibition of Na+/K+- ATPase with a complimentary mechanism that facilitates myocardial relaxation through activation of the SERCA2a calcium pump on the sarcoplasmic reticulum enhancing calcium reuptake from the cytoplasm. Data from multiple Phase 2 studies in patients with early cardiogenic shock or acute decompensated heart failure demonstrate that istaroxime infused intravenously significantly improves cardiac function and blood pressure without increasing heart rate or the incidence of cardiac rhythm disturbances.

About Windtree Therapeutics, Inc.
Windtree Therapeutics, Inc. is advancing late-stage interventions for cardiovascular disorders to treat patients in moments of crisis. Using new scientific and clinical approaches, Windtree is developing a multi-asset franchise anchored around compounds with an ability to activate SERCA2a, with lead candidate, istaroxime, being developed as a first-in-class treatment for cardiogenic shock and acute decompensated heart failure. Windtree’s heart failure platform includes follow-on pre-clinical SERCA2a activator assets as well. In pulmonary care, Windtree has focused on facilitating the transfer of the KL4 surfactant platform, to its licensee, Lee’s Pharmaceutical (HK) Ltd. and Zhaoke Pharmaceutical (Hefei) Co. Ltd. Included in Windtree’s portfolio is rostafuroxin, a novel precision drug product targeting hypertensive patients with certain genetic profiles.

Forward Looking Statements
This press release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. The Company may, in some cases, use terms such as "predicts," "believes," "potential," "proposed," "continue," "estimates," "anticipates," "expects," "plans," "intends," "may," "could," "might," "will," "should" or other words that convey uncertainty of future events or outcomes to identify these forward-looking statements. Such statements are based on information available to the Company as of the date of this press release and are subject to numerous important factors, risks and uncertainties that may cause actual events or results to differ materially from the Company’s current expectations. Examples of such risks and uncertainties include: risks and uncertainties associated with the success and advancement of the clinical development programs for istaroxime and the Company’s other product candidates; the Company’s ability to secure significant additional capital as and when needed; the Company’s ability to access the debt or equity markets; the Company’s ability to manage costs and execute on its operational and budget plans; the results, cost and timing of the Company’s clinical development programs, including any delays to such clinical trials relating to enrollment or site initiation; risks related to technology transfers to contract manufacturers and manufacturing development activities; delays encountered by the Company, contract manufacturers or suppliers in manufacturing drug products, drug substances, and other materials on a timely basis and in sufficient amounts; risks relating to rigorous regulatory requirements, including that: (i) the U.S. Food and Drug Administration or other regulatory authorities may not agree with the Company on matters raised during regulatory reviews, may require significant additional activities, or may not accept or may withhold or delay consideration of applications, or may not approve or may limit approval of the Company’s product candidates, and (ii) changes in the national or international political and regulatory environment may make it more difficult to gain regulatory approvals and risks related to the Company’s efforts to maintain and protect the patents and licenses related to its product candidates; risks that the Company may never realize the value of its intangible assets and have to incur future impairment charges; risks related to the size and growth potential of the markets for the Company’s product candidates, and the Company’s ability to service those markets; the Company’s ability to develop sales and marketing capabilities, whether alone or with potential future collaborators; the rate and degree of market acceptance of the Company’s product candidates, if approved; the economic and social consequences of the COVID-19 pandemic and the impacts of political unrest, including as a result of geopolitical tension, including the conflict between Russia and Ukraine, the People’s Republic of China and the Republic of China (Taiwan), and the evolving events in Israel and Gaza, and any sanctions, export controls or other restrictive actions that may be imposed by the United States and/or other countries which could have an adverse impact on the Company’s operations, including through disruption in supply chain or access to potential international clinical trial sites, and through disruption, instability and volatility in the global markets, which could have an adverse impact on the Company’s ability to access the capital markets. These and other risks are described in the Company’s periodic reports, including its Annual Report on Form 10-K, Quarterly Reports on Form 10-Q and Current Reports on Form 8-K, filed with or furnished to the Securities and Exchange Commission and available at www.sec.gov. Any forward-looking statements that the Company makes in this press release speak only as of the date of this press release. The Company assumes no obligation to update forward-looking statements whether as a result of new information, future events or otherwise, after the date of this press release.

Contact Information:
Eric Curtis
ecurtis@windtreetx.com


The ticker symbol for Windtree Therapeutics, Inc. is WINT.

Windtree Therapeutics, Inc. is exploring strategic alternatives such as acquisition, merger, further licensing, or company sale to maximize shareholder value.

Windtree Therapeutics, Inc. has made significant progress in advancing its cardiovascular portfolio, including clinical trials in cardiogenic shock and a licensing deal with Lee’s Pharmaceuticals for the Greater China-Asia Pacific region.

Craig Fraser is the President and Chief Executive Officer of Windtree Therapeutics, Inc.

The goal of engaging Ladenburg Thalmann & Co. Inc. is to evaluate strategic alternatives for the company with the goal of maximizing stockholder value.
Windtree Therapeutics Inc

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Biological Product (except Diagnostic) Manufacturing
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Biotechnology, Health Technology, Manufacturing, Biological Product (except Diagnostic) Manufacturing

About WINT

windtree therapeutics, inc. is a biotechnology company focused on developing novel kl4 surfactant therapies for respiratory diseases and other potential applications. windtree’s proprietary technology platform includes a synthetic, peptide-containing surfactant (kl4 surfactant ) that is structurally similar to human pulmonary surfactant — and novel drug-delivery technologies that are being developed to enable noninvasive administration of aerosolized kl4 surfactant. windtree is focused initially on improving the management of respiratory distress syndrome (rds) in premature infants as surfactant therapy has been shown to save lives in this condition. windtree believes that its proprietary technologies may make it possible, over time, to develop a pipeline of kl4 surfactant product candidates to address a variety of respiratory diseases for which there are few or no approved therapies and, in doing so, potentially deliver a lifetime of hope to patients and their families.