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TAXIS Pharmaceuticals Receives NIH SBIR Grant to Advance Development of Novel Antibiotic Class for Clostridioides difficile Infections


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TAXIS Pharmaceuticals

Aug 17, 2026, 08:29 ET

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Grant marks the company's third NIH SBIR award in just over two years and supports development of a narrow-spectrum investigational therapy targeting hypervirulent C. difficile strains.

MIAMI, Aug. 17, 2026 /PRNewswire-PRWeb/ -- TAXIS Pharmaceuticals, a clinical-stage company at the forefront of developing investigational therapies to treat multidrug-resistant bacterial infections and combat antimicrobial resistance (AMR), announced today that it has received a Phase I Small Business Innovation Research (SBIR) grant from the National Institute of Allergy and Infectious Diseases (NIAID), one of the institutes of the National Institutes of Health (NIH). The grant is valued at approximately $562,037, with the potential for up to $3 million in additional Phase II funding upon successful achievement of program milestones.

The grant will support the development of TAXIS Pharmaceuticals' investigational 3-alkoxy benzamide class of narrow-spectrum FtsZ inhibitors designed to combat Clostridioides difficile (C. difficile), including toxigenic and hypervirulent strains associated with severe disease and high recurrence rates. The award represents the company's third NIH SBIR grant in 27 months and will support continued advancement of its investigational FtsZ inhibitor program, which targets one of the most significant unmet needs in infectious disease.

"This NIH award further validates our scientific approach and strengthens our efforts to develop innovative therapies for some of the most challenging bacterial infections facing patients today." -- Gregory G. Mario, MBA, President and CEO

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"This NIH award further validates our scientific approach and strengthens our efforts to develop innovative therapies for some of the most challenging bacterial infections facing patients today," says Gregory G. Mario, MBA, President and CEO of TAXIS Pharmaceuticals. "Receiving our third NIH SBIR grant in just over two years reflects both the quality of our science and the urgent need for new therapeutic options to address antimicrobial resistance and serious infectious diseases."

C. difficile infection (CDI) is responsible for an estimated 500,000 illnesses and 30,000 deaths in the United States each year.(1) Hypervirulent strains have contributed to increasingly severe disease, while recurrence remains a major concern for patients and healthcare providers. Current frontline therapies, including metronidazole, vancomycin, and fidaxomicin, are broad-spectrum antibiotics that can disrupt the gut microbiome, potentially creating conditions that allow C. difficile to re-establish and contribute to recurrent infection.(2)

TAXIS Pharmaceuticals' investigational FtsZ inhibitors are designed to selectively target toxigenic and hypervirulent C. difficile strains while preserving beneficial gut bacteria. FtsZ, an essential bacterial cell division protein not found in human cells, represents an attractive target for antibiotic development. The company's proprietary 3-alkoxy benzamide scaffold has demonstrated potent activity against hypervirulent and drug-resistant C. difficile strains in preclinical studies.

By preserving the integrity of the gut microbiome, TAXIS' investigational approach aims to address one of the key challenges associated with CDI treatment: recurrence. The company believes this differentiated strategy may offer an important advancement over existing broad-spectrum therapies.

"Our investigational FtsZ inhibitor program represents a novel approach to treating C. difficile infections by selectively targeting pathogenic strains while preserving the beneficial bacteria that support a healthy gut microbiome," says Ajit Parhi, PhD, Chief Scientific Officer of TAXIS Pharmaceuticals and Principal Investigator on the project. "This NIH grant will allow us to advance critical preclinical development activities and further evaluate the potential of this program."

In May of 2025, TAXIS received a $2.9 million NIH grant to advance development of its dihydrofolate reductase inhibitors (DHFRIs) for multidrug-resistant gonorrhea. In May of 2024, TAXIS received a $2.67 million NIH grant to support development of its investigational efflux pump inhibitors (EPIs) designed to restore the effectiveness of existing antibiotics against resistant bacterial infections. Together with its FtsZ inhibitor platform, these programs reflect TAXIS' broader mission to develop innovative solutions to address the escalating global burden of antimicrobial resistance.

Research mentioned in this press release was supported by the National Institute of Allergy and Infectious Diseases of the National Institutes of Health Under Award Number 1R43AI197297-01. The content is solely the responsibility of the authors and does not necessarily represent the views of the National Institutes of Health.

About TAXIS Pharmaceuticals

TAXIS Pharmaceuticals is a clinical-stage company developing new classes of anti-resistance therapies to treat life-threatening, multidrug-resistant bacterial infections. Our investigational drug candidates—including efflux pump inhibitors, dihydrofolate reductase inhibitors, and FtsZ inhibitors—aim to combat antimicrobial resistance (AMR). TAXIS' investigational therapies currently target several different bacterial pathogens, many of which are on the World Health Organization Priority Pathogen List. Our mission is to reduce and potentially eliminate the threat of current and emergent antimicrobial resistant bacteria across a wide range of infectious diseases and save lives. To learn more, visit taxispharma.com.

Forward-Looking Statements

Investors and stakeholders should be aware that this press release contains forward-looking statements and information. Forward-looking statements are subject to known and unknown risks, uncertainties, and other factors that may cause our or our industry's actual results, levels or activity, performance or achievements to be materially different from those anticipated by such statements. The use of words such as "may", "might", "will", "should", "could", "expect", "plan", "anticipate", "believe", "estimate", "project", "intend", "future", "potential" or "continue", and other similar expressions are intended to identify forward looking statements.

For example, all statements we make regarding (i) the initiation, timing, cost, progress and results of our preclinical and clinical studies and our research and development programs, (ii) our ability to advance product candidates into, and successfully complete, clinical studies, (iii) the timing or likelihood of regulatory filings and approvals, (iv) our ability to develop, manufacture and commercialize our product candidates and to improve the manufacturing process, (v) the rate and degree of market acceptance of our product candidates, (vi) the size and growth potential of the markets for our product candidates and our ability to serve those markets, and (vii) our expectations regarding our ability to obtain and maintain intellectual property protection for our product candidates, are forward looking.

All forward-looking statements are based on current estimates, assumptions and expectations by our management that, although we believe to be reasonable, are inherently uncertain. All forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those that we expected. Any forward-looking statement speaks only as of the date on which it was made.

We undertake no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events or otherwise, except as required by law. This press release is not, and nothing in it should be construed as, an offer, invitation or recommendation in respect of our securities, or an offer, invitation or recommendation to sell, or a solicitation of an offer to buy, any of our securities in any jurisdiction. Neither this press release nor anything in it shall form the basis of any contract or commitment. This press release is not intended to be relied upon as advice to investors or potential investors and does not take into account the investment objectives, financial situation or needs of any investor.

References:

1. Feuerstadt P, Theriault N, Tillotson G. "The burden of CDI in the United States: a multifactorial challenge." BMC Infect Dis. 2023 Mar 7;23(1):132. Accessed 8 June 2026.

2. Sehgal K, Khanna S. "Gut microbiome and Clostridioides difficile infection: a closer look at the microscopic interface." Ther Adv Gastroenterol. 2021 Feb 23;14:1756284821994736. Accessed 8 June 2026.

Media Contact

Jennifer Ringler, TAXIS Pharmaceuticals, 1 973-647-5004, [email protected], https://taxispharma.com/

SOURCE TAXIS Pharmaceuticals

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