$3.3M to Fund Trial of Ai-Designed Bacteriophage Therapy for HAP/VAP
$3.3M to Fund Trial of Ai-Designed Bacteriophage Therapy for HAP/VAP
Locus Biosciences will conduct a clinical trial for its Ai-designed bacteriophage therapeutic for HAP/VAP caused by antibiotic-resistant P. aeruginosa.
RT’s Three Key Takeaways:
- Federal support for phage therapy – Locus Biosciences received a $3.3 million NIAID contract, with potential expansion to $28 million, to advance a Phase 1b clinical trial of its engineered bacteriophage LBP-PA01 for antibiotic-resistant Pseudomonas aeruginosa pneumonia.
- AI-designed precision antibacterial – LBP-PA01 was developed using Locus’s AI- and robotics-driven platform, which rapidly designs and optimizes engineered bacteriophage cocktails to selectively kill drug-resistant bacteria.
- Addressing a critical public health threat – The program targets hospital-acquired and ventilator-associated pneumonia, major ICU killers for which antibiotic-resistant P. aeruginosa is a CDC-designated serious threat with limited effective treatment options.
Locus Biosciences was awarded a $3.3 million contract by the National Institute of Allergy and Infectious Diseases (NIAID) to support a proof-of-concept clinical trial of LBP-PA01, an AI-designed bacteriophage therapeutic for hospital-acquired pneumonia (HAP) and ventilator-associated pneumonia (VAP) caused by antibiotic-resistant Pseudomonas aeruginosa bacteria.
The company says the contract could with further funding of up to a total of $28 million available over the course of the contract if all project milestones are met. The awarded contract will
Under contract No. 75N93025C00035, NIAID will fund a Phase 1b clinical trial of LBP-PA01, enabling Locus to evaluate safety, efficacy, and optimal dosing in patients with P. aeruginosa infections that have become increasingly difficult to treat using conventional antibiotics.
Locus created LBP-PA01 using its AI-driven discovery engine, where robotics and machine learning converge to rapidly design next-generation engineered bacteriophage therapies. This platform experimentally measures millions of phage-bacteria interactions and uses these outcomes to simulate over a quadrillion (one million billion) potential phage combinations in silico, identifying the most effective therapeutic cocktail candidates. Within this framework, multimodal large language models trained on genomic and functional datasets predict optimal genomic engineering configurations for incorporating antibacterial payloads, enabling precise synthetic biology optimization of phage genomes to enhance the killing of target pathogens. By integrating automation and AI, the Locus platform compresses what once took years of trial-and-error into weeks of systematic testing, enabling a rapid response to emerging drug-resistant pathogens.
“Partnering with HHS to advance multiple programs under NIAID and BARDA is an exciting evolution for Locus as we deploy our platform to deliver precision antibacterial therapies across diverse indications and routes of administration,” said Paul Garofolo, CEO of Locus Biosciences. “With NIAID driving innovation targeting respiratory infections and BARDA advancing solutions for urinary tract infections, we are united under a shared mission to solve the global antimicrobial resistance crisis. This collaboration underscores the power of Locus’s AI-enabled drug development platform and its advanced U.S.-based manufacturing to accelerate a new generation of engineered bacteriophage therapeutics.”
Hospital-acquired pneumonia (HAP) is among the most serious and common healthcare-associated infections, accounting for approximately 15–20% of hospital-onset infections and remains a leading cause of mortality in intensive care units. P. aeruginosa is a frequent cause of HAP and ventilator-associated pneumonia (VAP), responsible for up to 24% of ICU respiratory infections in some studies. The U.S. Centers for Disease Control and Prevention (CDC) has identified antibiotic-resistant P. aeruginosa as a serious public health threat, underscoring the urgent need for precision therapies to combat this pathogen.
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