Windtree Files Istaroxime Cardiogenic Shock and Prevention of Arrythmias Patent for India
28 February 2025 - 12:00AM
Windtree Therapeutics, Inc. (“Windtree” or the “Company”)
(NasdaqCM: WINT), a biotechnology company focused on advancing
early and late-stage innovative therapies for critical conditions
and diseases, announced today that the Company has filed a national
phase patent application with the Indian patent office claiming
priority to PCT/US2024/058923 entitled, “ISTAROXIME AND DERIVATIVES
THEREOF FOR PREVENTING OR REDUCING THE RISK OF ACUTE MYOCARDIAL
ARRHYTHMIA.”
Arrythmias are irregular heartbeats that can impact the pumping
function of the heart. Patients with heart failure and
cardiomyopathy are at risk for arrythmias. Arrythmias in these
patients can be caused by their underlying cardiac disease or by
drugs used to treat the heart failure such as catecholamines.
Arrythmias can impair proper filling of the heart with blood and,
importantly, cardiac output to the body. Ventricular arrythmias are
particularly dangerous and can be fatal.
“India’s population is greater than 1.4 billion people making it
a part of our istaroxime strategic intellectual property plan,”
said Jed Latkin, CEO of Windtree. “As we prepare for Phase 3
readiness in cardiogenic shock, we plan to obtain intellectual
property protection in key markets such as India.”
About IstaroximeIstaroxime is a first-in-class
dual-mechanism therapy designed to improve both systolic and
diastolic cardiac function. Istaroxime is designed as 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 have demonstrated 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 a biotechnology company focused on advancing
early and late-stage innovative therapies for critical conditions
and diseases. Windtree’s portfolio of product candidates includes
istaroxime, a Phase 2 candidate with SERCA2a activating properties
for acute heart failure and associated cardiogenic shock,
preclinical SERCA2a activators for heart failure and preclinical
precision aPKCi inhibitors that are being developed for potential
in rare and broad oncology applications. Windtree also has a
licensing business model with partnership out-licenses currently in
place.
Forward Looking StatementsThis press release
contains statements related to the potential clinical effects of
istaroxime; the potential benefits and safety of istaroxime; the
clinical development of istaroxime; and our research and
development program for treating patients in early cardiogenic
shock due to heart failure. Such statements constitute
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. The
Company cannot assure that any patent will issue as a result of a
pending patent application or, if issued, whether it will issue in
a form that will be advantageous to the Company. Examples of such
risks and uncertainties include, among other things: the Company’s
ability to acquire revenue generating subsidiaries; the market’s
reaction to potential acquisitions by the Company; the Company’s
ability to secure significant additional capital as and when
needed; the Company’s ability to achieve the intended benefits of
the aPKCi asset acquisition with Varian Biopharmaceuticals, Inc.;
the Company’s risks and uncertainties associated with the success
and advancement of the clinical development programs for istaroxime
and the Company’s other product candidates, including preclinical
oncology candidates; 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 the Middle East, 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
Curtisecurtis@windtreetx.com
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