Project Grant R44AI197713
- The National Institute of Allergy and Infectious Diseases awarded Brown University $542,599 on July 6, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to develop bacteria-responsive hydrogel wound dressings for on-demand delivery of antibiotics and probiotics targeting chronic wound infections caused by methicillin-resistant Staphylococcus aureus and Pseudomonas aeruginosa. The project addresses antibiotic resistance and biofilm formation in chronic wounds by...
- The National Institute of Allergy and Infectious Diseases awarded Georgia TECH Research Corp $149,190 on January 23, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to investigate R-pyocins as a therapeutic approach to treat high-risk, multidrug-resistant Pseudomonas aeruginosa wound infections. The project addresses the rising prevalence of multidrug-resistant and extensively drug-resistant P. aeruginosa strains that cause acute and chronic infections from...
- The National Institute of Allergy and Infectious Diseases awarded Purdue University $442,500 on September 3, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to develop antimicrobial agents derived from aapeptide biomaterials targeting drug-resistant bacterial infections. The research addresses antimicrobial resistance identified by the World Health Organization as a major twenty-first-century threat. Purdue will develop small-molecule scorpion-like amphipathic...
- This Project Grant award from the National Institute of Allergy and Infectious Diseases (NIAID), under the Allergy and Infectious Diseases Research program (CFDA 93.855), provides $474,363.00 to Rowan University to develop novel antimicrobial peptides inspired by the clinically approved compound daptomycin. The goal is to create new peptide molecules that mimic daptomycin's key mechanisms of action, such as calcium binding and lipid membrane disruption, while improving resistance to...
- The National Institute of Allergy and Infectious Diseases awarded the University of Massachusetts $2,641,186 on April 1, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to develop antimicrobial poly(oxanorborneneimide) polymers (PONI-AMPs) for treating multidrug-resistant wound biofilm infections. The research integrates synthetic chemistry, atomistic computational modeling, and machine learning to evolve PONI-AMP therapeutics. Initial work demonstrated 99...
- The National Institute of Allergy and Infectious Diseases awarded Virginia Polytechnic Institute & State University $808,607 on July 9, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to optimize AI-designed antimicrobial peptides targeting ESKAPE pathogens. The project integrates artificial intelligence, machine learning, chemical approaches, and computational tools to develop peptide-based therapeutics against multidrug-resistant bacteria including...
- The National Institute of Allergy and Infectious Diseases, part of the Department of Health and Human Services, awarded $599,327 to Microbiotix, Inc. on September 22, 2025, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to develop novel benzyl-piperidine antifungal agents targeting intractable mucormycosis infections caused by drug-resistant Mucorales fungi. The project focuses on chemical optimization of a benzyl-piperidine series to improve drug-like properties and...
- The National Institute of Allergy and Infectious Diseases awarded Sciogen LLC $314,363 on September 1, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to develop novel therapeutics targeting respiratory syncytial virus (RSV) infection through G-receptor binding inhibition. The Phase I Small Business Innovation Research award funds evaluation of a new class of RSV inhibitors identified through high-throughput screening. Work includes assessment of biological...
- The National Institute of Allergy and Infectious Diseases awarded Chitozan Health, LLC $320,600 on September 1, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to develop innovative flame-retardant antimicrobial textiles for healthcare and protective applications. Chitozan Health will develop a dual-function textile finish combining antimicrobial and flame-retardant properties by leveraging chitosan and 0.25-micron silver chloride particles. The work involves...
- The National Institute of Allergy and Infectious Diseases awarded the University of California, San Diego $720,035 on February 2, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to develop living microrobot therapeutics for treating severe multidrug-resistant pulmonary infections. The project centers on designing and validating a microrobot platform consisting of Chlamydomonas reinhardtii microalgae modified with neutrophil membrane-coated, drug-loaded polymeric...
The National Institute of Allergy and Infectious Diseases awarded Riptide Bioscience, Inc., $1 million on August 1, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to develop RP557, a designed host defense peptide for topical treatment of burn wound infections. RP557 is a chemically derived antimicrobial peptide that exhibits broad activity against gram-positive and gram-negative bacteria, fungi, and biofilm-forming organisms. Preclinical studies demonstrated potent efficacy in a clinically relevant polymicrobial infected full-thickness thermal porcine burn model and rodent models, suppressed inflammatory responses, accelerated wound healing, and showed good tolerability in a 14-day GLP rat toxicology study. The funded work encompasses regulatory-enabling chemistry, manufacturing, and preclinical studies intended to support clinical translation. The award runs through July 31, 2029, with performance at Riptide Bioscience's location in Vallejo, California. The assistance type is a Project Grant. Burn infection remains a leading cause of morbidity and mortality in burn patients due to loss of skin barrier function and increased vulnerability to infection; the rising prevalence of multidrug-resistant organisms and biofilm formation limit current antibiotic effectiveness. RP557's mechanism renders bacterial resistance unlikely, positioning it as a potential first-line empiric treatment that could improve patient outcomes while reducing costs to patients, families, hospitals, and society.
Mod # | Description | ReasonForModification | Federal Obligation | Date |
|---|---|---|---|---|
| Not listed | $1.0m | 8/1/26 |