• 6 September 2016
    Arsanis Announces Two Key Publications Supporting Its Lead Program ASN100

    WALTHAM, Mass. and VIENNA, Austria – September 6, 2016 – Arsanis, Inc., a clinical-stage biotechnology company developing targeted monoclonal antibodies (mAbs) for pre-emptive treatment and therapy of serious infectious diseases, today announced two scientific publications in the journals Antimicrobial Agents and Chemotherapy (AAC) and mAbs. Together, these two publications confirm the activity of ASN-1 and ASN-2, the human monoclonal antibodies that comprise Arsanis’ lead clinical candidate, ASN100, targeted against Staphylococcus aureus pneumonia. 

    S. aureus is a common organism that can live on the skin or in the nasal passages of humans and is frequently the cause of serious and life threatening infections. S. aureus secretes an arsenal of different toxins that damage epithelial cells and disrupt the human immune response, and in particular destroy human immune cells needed for defense against infections. ASN100 acts by broadly neutralizing six relevant S. aureus cytotoxins implicated in the pathogenesis of serious infections such as pneumonia. Traditional antibiotics do not neutralize these toxins, and this may contribute to the high mortality rates frequently reported in patients with S. aureus pneumonia.

    The data published in AAC demonstrate that ASN-1, a unique, broadly cross-reactive human mAb that neutralizes five of six important S. aureus cytotoxins, displays superior protective efficacy against severe S. aureus pneumonia in an established rabbit model when compared with a single-toxin neutralizing mAb targeting only Hla. These data also show that the rabbit pneumonia model is more clinically relevant than traditional murine models as mice are insensitive to the effects of S. aureus leukocidins while rabbits more closely mimic human sensitivity. The second scientific paper published in mAbs describes the challenging but successful path to Arsanis’ discovery of ASN-2, a highly potent human mAb that is uniquely able to inactivate LukGH (including sequence variants). LukGH is the sixth S. aureus cytotoxin implicated in pneumonia pathogenesis.

    “We believe that the combined action of ASN-1 and ASN-2 positions ASN100 to effectively address all strains of S. aureus as the only mAb product in development that neutralizes six human cytotoxins that are key to the pathogenesis of serious infections such as pneumonia,” said Eszter Nagy, M.D., Ph.D., cofounder and Chief Scientific Officer, Arsanis. “ASN100 has the potential to offer a novel, precision approach to address serious and life-threatening infections in high-risk patients.”

    “The addition of non-antibiotic and pre-emptive approaches like ASN100 to the antibacterial armamentarium should be critical in the face of high mortality and increasing antibiotic resistance globally,” said David Mantus, Ph.D., Chief Development officer. “We are looking forward to initiating our Phase 2 study of ASN100 later this year.”

    Please refer to AAC’s online publication for more information about the ASN-1 study, and mAbs’ online publication for more information about ASN-2 discovery.