Next Generation Polymyxin Antibiotics: Optimization and Validation
The NOVA ERC PoC project aims to develop and validate novel semi-synthetic polymyxins as safer, effective alternatives for treating multi-drug-resistant Gram-negative infections, culminating in a business plan.
Projectdetails
Introduction
In the NOVA ERC PoC project, we present a novel class of semi-synthetic polymyxins as an innovative solution to address the inherent toxicity of the polymyxins family of antibiotics. We here disclose the first candidate compounds of this novel family of antibiotics with potential for use as front-line treatment for multi-drug-resistant Gram-negative bacterial infections.
Background
Due to antimicrobial resistance (AMR), a resurgence in the use of polymyxin antibiotics has occurred over the last decade, despite the well-characterized and dose-limiting nephrotoxicity associated with these compounds. Though designated as last-resort antibiotics due to these side effects, the ongoing rise of AMR is forcing clinicians to rely on unsafe antibiotics such as the polymyxins. Increased polymyxin use results in risks for patients and pressure on healthcare systems.
Advantages of Novel Polymyxins
Our novel semi-synthetic polymyxins have best-in-class potential given their significantly improved safety profile and offer a superior alternative to current last-resort anti-Gram-negative antibiotics. Succinctly, the next generation polymyxins we have developed offer key advantages over current last-resort antibiotics:
- Reduced nephrotoxic side effects
- Effectiveness against multi-resistant strains with negligible resistance induction
- Ability to be produced at low cost
Moreover, our robust semisynthetic approach will allow us to generate additional analogues in the future.
Project Goals
In NOVA, we will explore the technical and commercial potential of our next generation polymyxins. Specifically, we will validate the first candidate compounds and perform preliminary preclinical toxicity studies in vivo.
Commercial Evaluation
In parallel, we will evaluate the commercial feasibility of the next generation polymyxins. This entails analyzing the market and (existing and emerging) competitors, as well as the IP position and strategy.
Conclusion
By the end of the project, we will consolidate the project outcomes in an investor-ready business plan.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 150.000 |
Totale projectbegroting | € 150.000 |
Tijdlijn
Startdatum | 1-11-2022 |
Einddatum | 30-4-2024 |
Subsidiejaar | 2022 |
Partners & Locaties
Projectpartners
- UNIVERSITEIT LEIDENpenvoerder
Land(en)
Geen landeninformatie beschikbaar
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Project PREVAIL aims to validate the novel antibiotic Laterocidamide (LATERO) against polymyxin-resistant Gram-negative bacteria, addressing antibiotic resistance while exploring its commercial potential.
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This project aims to optimize and evaluate a novel DnaN inhibitor, WAM-N17, to develop new antibiotics targeting multidrug-resistant bacteria through compound synthesis and in vivo studies.
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The PoC4ProMis project aims to demonstrate in vivo efficacy of novel cyclic peptides for ALS using optimized CNS delivery methods, while strengthening IP for potential neurodegenerative disease treatments.
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