Alopexx today announced that it has completed a Phase I clinical trial with AV0328, a vaccine targeting the broadly expressed microbial antigen, poly-N-acetyl glucosamine.
Potential to prevent wide range of infections including those caused by antibiotic-resistant organisms.
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[25-October-2017] |
CONCORD, Mass., Oct. 25, 2017 /PRNewswire/ -- Alopexx Vaccine today announced that it has completed a Phase 1 clinical trial with AV0328, a vaccine targeting the broadly expressed microbial antigen, poly-N-acetyl glucosamine (PNAG). Antibodies to PNAG have the potential to prevent many serious and life-threatening infections such as pneumonia, meningitis, bloodstream infections, gonorrhea, and also those caused by antibiotic resistant bacteria such as MRSA. The World Health Organization has warned that the increasing development of numerous antibiotic-resistant “superbugs” pose an enormous threat to human health. Based on these results, Alopexx plans to initiate a Phase 2 clinical study with AV0328 in the first quarter of 2018. “We are very encouraged by these early clinical data demonstrating the safety, tolerability and initial indications of clinical activity of AV0328 in humans,” said Hal Landy, M.D., Chief Medical Officer at Alopexx. “We look forward to further evaluating AV0328 against a breadth of infections caused by PNAG-expressing pathogens, including serious soft-tissue infections caused by methicillin-resistant S. aureus (MRSA), pneumonia, meningitis, tuberculosis and sexually transmitted diseases, including those caused by antibiotic-resistant organisms.” “Our modified, synthetic vaccine that targets natural PNAG expressed on the surface of most pathogenic bacteria, as well as important eukaryotic pathogens like malaria and numerous fungi, could represent a new paradigm for disease prevention by inducing protection against a large number of infectious agents, including those manifesting high levels of antibiotic resistance” Gerald B. Pier, Professor of Medicine, Harvard Medical School, Microbiologist, Brigham and Women’s Hospital. About the Phase 1 Clinical Study AV0328 was safe and well-tolerated in this study with only minor and transient injection site reactions observed in each dose group. At the two highest doses (75 mg and 150 mg), clear increases were noted in antibody titers against PNAG, as well as a positive indication of protective immunity, as measured by complement activation and binding to the PNAG antigen. In addition, robust bactericidal killing of N. gonorrhea, including antibiotic-resistant strains, and N. meningitidis (serogroups A, B, C, W, Y), as well as opsonic killing of S. pneumoniae, multi-drug resistant Klebsiella pneumonia, colistin and multi-drug resistant strains of E. coli and S. aureus, including MRSA clinical isolates, was observed. About AV0328 About Alopexx Vaccine LLC Contacts: or Gina Nugent, Nugent Communications
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