About This Project
Drug-resistant tuberculosis (TB) is a consistently growing threat to global health. We have developed Oxy291, a new, orally available antibiotic that targets both active and dormant (persistent) TB bacteria. This project will test Oxy291 in mice to determine if it can safely and effectively reduce TB infection, paving the way for developing faster, more effective treatments.
Ask the Scientists
Join The DiscussionWhat is the context of this research?
Every year, TB takes over a million lives, more than any other infectious disease. For countless families, a TB diagnosis means fear, isolation, and months to years of toxic treatments with no guarantee of a cure. As drug-resistant strains spread, the world faces a mounting crisis. Existing therapies are lengthy, harsh, and often fail to clear dormant, “persister” bacteria, leading to relapse and ongoing transmission. New hope is urgently needed. Oxy291 is a novel antibiotic we have been developing and improving over the last two years. Oxy291 selectively targets Mycobacterium tuberculosis, the bacteria that cause TB, including drug-resistant and dormant forms. Early lab work shows Oxy291 is potent, safe for human cells, and accumulates in the lungs where TB infection is most severe. However, its effectiveness in infected living animals has not been tested. This project aims to fill that gap by evaluating Oxy291 in a mouse model of TB, a critical step before advancing to human studies.
What is the significance of this project?
Our drug candidate, Oxy291, represents newfound hope in the battle against this debilitating and fatal disease. Oxy291 is a new class of antibiotic with a unique mechanism of action, designed to overcome resistance and target hard-to-kill bacteria. If successful, this work could lay the foundation for shorter, safer, and more effective TB therapies with the ultimate goals of reducing the global burden of disease, saving lives, and slowing the spread of resistant infections. By supporting this project, you are not just advancing science, you are giving hope to millions who are desperately in need of a better solution.
What are the goals of the project?
Our goal is to test the ability of Oxy291 to reduce TB infection in vivo. C57BL/6 mice will be infected with Mycobacterium tuberculosis (Mtb), after 21 days to establish infection, each group (5 mice/group) will begin treatment with 1) 50 mg/kg Oxy291, 2) 200 mg/kg Oxy291, 3) vehicle (negative control), and 4) 10mg/kg INH (positive control) by once daily oral gavage. At two timepoints, after 30 and 60 days of treatment, the number of Mtb bacteria in the lung will be enumerated by CFU assay. Mice will be monitored and weighed daily. If Oxy291 shows strong efficacy and is well-tolerated, we will have the critical proof needed to move forward with further development and attracting additional support. All results will be shared openly with the scientific community and our supporters, ensuring your contribution advances the frontier of knowledge and empowers fellow scientists worldwide.
Budget
Mice and housing are required for the experiment. Compound synthesis ensures we have enough Oxy291 for all tests. Infection and safety procedures are needed for handling TB bacteria safely. Bacterial analysis allows us to measure treatment effects, and data/reporting ensures results are shared transparently. Please note: this budget is about half of the actual cost for the experiment; the remainder will be paid for by our team bootstrapping since our young company has not raised any funding yet mainly because we don't have in vivo data. So, surpassing the $11K goal would be very helpful in advancing our research even further. Thank you!
Endorsed by
Project Timeline
This study represents the first time that a bactericidal oxysterol will ever be tested for efficacy in mice; and if successful, will be a critical milestone on the path to human trials, marking significant achievement for validating its potential as a novel chemical class and setting the foundation for the future antibiotic discovery and development. All milestones will be documented with lab notes, and updates will be promptly sent to backers.
Apr 30, 2025
Project Launched
Jun 16, 2025
Synthesis of Oxy291
Jun 18, 2025
Infect mice
Jul 09, 2025
Begin treatments
Sep 08, 2025
Complete treatments and collect all samples
Meet the Team
Team Bio
Philip Sell: LinkedIn, ResearchGate
Jaejin (Joey) Lee: LinkedIn, ResearchGate
Philip Sell
Philip was technically trained in microbiology and virology. He received his B.S. in Microbiology, Immunology, and Molecular Genetics from UCLA, and M.S. in Molecular Microbiology and Immunology from USC. His thesis work on the role of desaturase enzymes in adaptive survival mechanisms of Mycobacterium tuberculosis discovered new potential drug targets. He significantly contributed to the understanding of severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2) through projects ranging from brief pilot studies to extensive, multi-month endeavors, including efficacy of therapeutic compounds, testing antibodies against SARS-CoV-2, generating substantial datasets from clinical samples, and validating HVAC air purification systems. His research and experiences, and desire to develop novel therapies for debilitating and fatal human diseases, have led to the founding of Metaba. At Metaba, we aim to bring much needed innovation to treatment strategies for infectious diseases and to provide our expertise in metabolomics to help advance informative care solutions for population health.
Jaejin (Joey) Lee
Jaejin earned his Ph.D. in Molecular Biology from Myoungji University, Korea, where he developed a rapid method for detecting antibiotic resistance genes. As a postdoctoral researcher at the University of Southern California, he focused on the mechanisms of antibiotic resistance in microorganisms, particularly in Mtb during persister formation. His work has clarified molecular mechanisms of resistance, aiding in prevention, diagnosis, and treatment strategies, and has been published in leading journals like Nature Communications. Recently, he has developed new therapeutic approaches using lipidomics, transcriptomics, and metabolomics to study cell wall-mediated drug resistance. The promising results of this research have led Jaejin to co-found Metaba with Philip Sell to further develop and commercialize this technology and bring innovation to the treatment strategy for TB. It is his ongoing commitment to continue efforts and provide his expertise toward the development of novel therapeutics at Metaba.
Additional Information
Project Backers
- 24Backers
- 25%Funded
- $2,644Total Donations
- $110.17Average Donation