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      Pulmatrix Receives US Patent Covering iSPERSE™ Formulations for Pulmazole Program

      US Patent (Pat. No. 10376465) protects iSPERSE formulations for Pulmazole

      Pulmatrix logo (PRNewsFoto/Pulmatrix, Inc.)

      News provided by

      Pulmatrix, Inc.

      Aug 19, 2019, 09:25 ET

      Share this article

      Share this article


      LEXINGTON, Mass., Aug. 19, 2019 /PRNewswire/ -- Pulmatrix, Inc. (NASDAQ: PULM) has received a grant from the United States Patent and Trademark Office for US Pat. No. 10376465.  Granted claims cover iSPERSE formulations of the company's lead pipeline program Pulmazole.  The patent, entitled "Monovalent Metal Cation Dry Powders for Inhalation", protects formulations that contain an anti-fungal agent with iSPERSE formulations.  iSPERSE is Pulmatrix's proprietary inhaled engineered particle technology.

      "The expansion of our iSPERSE intellectual property rights in the United States builds upon our growing worldwide patent estate supporting our platform technology and our proprietary programs.  This patent is a valuable step in supporting the development of our lead anti-fungal program to serve unmet needs of patients worldwide," said Ted Raad, chief executive officer of Pulmatrix.

      About Pulmatrix
      Pulmatrix is a clinical stage biopharmaceutical company developing innovative inhaled therapies to address serious pulmonary disease using its patented iSPERSE™ technology. The Company's proprietary product pipeline is focused on advancing treatments for serious lung diseases, including Pulmazole, an inhaled anti-fungal for patients with allergic bronchopulmonary aspergillosis ("ABPA"), and PUR1800, a narrow spectrum kinase inhibitor for patients with obstructive lung diseases including asthma and chronic obstructive pulmonary disease ("COPD"). Pulmatrix's product candidates are based on iSPERSE™, its proprietary engineered dry powder delivery platform, which seeks to improve therapeutic delivery to the lungs by maximizing local concentrations and reducing systemic side effects to improve patient outcomes.

      FORWARD-LOOKING STATEMENTS
      Certain statements in this press release that are forward-looking and not statements of historical fact are forward-looking statements within the meaning of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements include, but are not limited to, statements of historical fact, and may be identified by words such as "anticipates," "assumes," "believes," "can," "could," "estimates," "expects," "forecasts," "guides," "intends," "is confident that", "may," "plans," "seeks," "projects," "targets," and "would," and their opposites and similar expressions are intended to identify forward-looking statements. Such forward-looking statements are based on the beliefs of management as well as assumptions made by and information currently available to management. Actual results could differ materially from those contemplated by the forward-looking statements as a result of certain factors, including, but not limited to, delays in planned clinical trials; the ability to establish that potential products are efficacious or safe in preclinical or clinical trials; the ability to establish or maintain collaborations on the development of therapeutic candidates; the ability to obtain appropriate or necessary governmental approvals to market potential products; the ability to obtain future funding for developmental products and working capital and to obtain such funding on commercially reasonable terms; the Company's ability to manufacture product candidates on a commercial scale or in collaborations with third parties; changes in the size and nature of competitors; the ability to retain key executives and scientists; and the ability to secure and enforce legal rights related to the Company's products, including patent protection. A discussion of these and other factors, including risks and uncertainties with respect to the Company, is set forth in the Company's filings with the SEC, including its annual report on Form 10-K filed with the Securities and Exchange Commission on February 19, 2019, as amended on July 24, 2019, as may be supplemented or amended by the Company's Quarterly Reports on Form 10-Q. The Company disclaims any intention or obligation to revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law.        

      Investor Contact


      Ted Raad, CEO

      William Duke, CFO       

      (781) 357-2333

      (781) 357-2333  

      rclarke@pulmatrix.com

      wduke@pulmatrix.com

      SOURCE Pulmatrix, Inc.

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