The goal of this clinical trial is to learn about the safety and tolerability of NTR-101 in adult participants suffering from acute alcohol-associated hepatitis (AH). The drug is intended for use in the treatment of AH where the presence of specific strains of E. faecalis play a contributing role. The main questions it aims to answer are: Are multiple doses of NTR-101 in participants with acute AH safe and well tolerated? What medical problems do participants have when taking NTR-101? Researchers will administer the drug and monitor participants in an inpatient center. Participants will: Be administered multiple ascending dose frequencies of NTR-101 every day for 7 days. Stay in the clinic for 9 days (7 days of treatment) and present to clinic once every week for checkups and tests for 35 days. Keep a diary of their symptoms until the checkups and tests are completed.
Alcohol-associated hepatitis (AH) is a severe inflammatory liver disease that can progress to liver failure, with high morbidity and mortality rates. Emerging studies indicate a significant role of gut-derived pathogens, particularly Enterococcus faecalis (E faecalis), in exacerbating liver damage through bacterial translocation and the release of toxins. Cytolysin-positive E. faecalis strains exhibit high virulence and resistance to standard antibiotics. NTR-101 is a product developed for oral delivery and composed of natural bacteriophages that specifically target cytolysin-positive E. faecalis. The targeted activity of NTR-101 against E. faecalis in AH patients has the potential to address the underlying bacterial trigger, offering a novel approach to mitigate liver inflammation and reduce disease progression. For patients who do not respond to traditional treatments like corticosteroids or experience reduced antibiotic therapy efficacy, NTR-101 represents a novel, targeted approach that leverages bacteriophages' specificity for bacterial strains in this target population, offering a potential alternative or complement to traditional antibiotics.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
12
NTR-101 will be given orally to participants once daily for 7 days
NTR-101 will be given orally to participants once daily for 7 days
NTR-101 will be given orally to participants twice daily for 7 days
NTR-101 will be given orally to participants three times daily for 7 days
Southern California Research Center, inc
Coronado, California, United States
Frequency of adverse events
The number of adverse events (AEs) will be recorded.
Time frame: AEs will be recorded daily for 7 days, then weekly on days 14, 21, 28 and 35
Changes in liver function will be evaluated
ALT (alanine transaminase) and AST (aspartate aminotransferase) enzymes will be evaluated
Time frame: Assessments will be recorded daily for 7 days, then weekly on days 14, 21, 28 and 35
Preliminary assessment of NTR-101 efficacy and viability
Assessment of relative abundance of target pathogen and NTR-101 viability after oral administration
Time frame: Stool samples will be collected daily for 7 days, then weekly on days 14, 21, 28 and 35 to evaluate the presence of the target pathogen and NTR-101 viability
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