checkAd

     278  49 Kommentare Recce Pharmaceuticals Announces Positive Data Against Streptococcus pneumoniae Sinusitis Infection in Animal Model - Seite 2


    NAD: No abnormality detected

    This bacterium was chosen due to its immediate availability as a recognized sinusitis model. Streptococcus pneumoniae, a Gram-positive bacterium, is a leading cause of bacterial pneumonia and meningitis in the United States, and a common cause of bloodstream infections, also known as sepsis, ear and sinus infections.2

    A total of 12 groups of 10 mice each were assessed to determine the effectiveness of R327 and R111 against S. pneumoniae. Three groups were treated with varying intranasal doses twice daily of R327 (50, 100, 500 mg/kg) and showed a significant dose-dependent antibacterial effect when compared to early infection and vehicle control (p<0.05).

    Three groups of mice were treated with varying intravenous doses of R327 (100, 500, 1,000 mg/kg) which showed significant dose-dependent antibacterial effect when compared to early infection control and vehicle control (p<0.05). Furthermore, three groups from the 12 were treated with varying intravenous doses of R111 (50, 100, 250 mg/kg) which showed a significant dose-dependent antibacterial effect when compared to early infection control and vehicle control (p<0.05).

    Azithromycin was the positive control in the study given twice daily at 200 mg/kg and showed bactericidal effect when compared to vehicle control at five-days post infection (p<0.05).

    The Company’s R327 and R111 compounds showed significant antibacterial capability with no abnormalities detected and are expected to be subject to further expanded sinusitis studies in due course. In addition to these studies, the Company’s clinical activities with R327 continues to progress in the background and looks forward to updating shareholders in due course.

    About Recce Pharmaceuticals Ltd

    Recce Pharmaceuticals Ltd (ASX:RCE, FSE:R9Q) is pioneering the development and commercialisation of New Classes of Synthetic Anti-Infectives designed to address the urgent global health problems of antibiotic resistant superbugs and emerging viral pathogens.

    Recce’s anti-infective pipeline is unique and comprised of broad-spectrum synthetic polymer antibiotics RECCE 327, RECCE 435 and RECCE 529 for viral infections with unique mechanisms of action against hyper-mutation on bacteria and viruses, respectively.

    Patented lead candidate RECCE 327 has been developed for the treatment of blood infections and sepsis derived from E. coli and S. aureus bacteria – including their superbug forms. Recce’s new antibiotic compound, RECCE 435, has been formulated for oral use.

    Seite 2 von 3


    Diskutieren Sie über die enthaltenen Werte


    globenewswire
    0 Follower
    Autor folgen

    Verfasst von globenewswire
    Recce Pharmaceuticals Announces Positive Data Against Streptococcus pneumoniae Sinusitis Infection in Animal Model - Seite 2 Highlights: Positive sinusitis infection data indicated in animal study Study supports broad spectrum potential of Recce’s anti-infective compounds against Streptococcus pneumoniae (S. pneumoniae) for both nasal and intravenous administration RECCE …

    Schreibe Deinen Kommentar

    Kommentare

    Avatar
    16.04.24 11:17:21
    Avatar
    08.04.24 16:11:34
    https://www.dgwa.org/post/recce-pharmaceuticals-news-asx-rce…

    • Vielversprechende Wirkung der Minimalen Hemmkonzentration (Minimum Inhibitory Concentration – „MIC“) in der Phase I/II UTI/Urosepsis-Studie mit einer Erhöhung der Dosierung, die in den nächsten Wochen beginnen soll
    • Ausweitung der klinischen Phase I/II-Studie mit DFI (diabetischem Fuß), deren Ergebnisse erreicht wurden. Phase III-Zulassungsstudie in Indonesien wird voraussichtlich in Q3 2024 beginnen
    • RECCE® 327 wurde gegen mehr als 300 Stämme bakterieller Krankheitserreger getestet und erwies sich während der Tests bei Linnaeus Bioscience als wirksam gegen alle.
    • Das US-Verteidigungsministerium hat RECCE® 327 Gel (R327G) als topische Behandlung von Infektionen bei Brandwunden für eine Förderung in Höhe von 2,2 Mio. USD (ca. 3,34 Mio. AUD) empfohlen
    • Antrag auf Zulassung eines neuen Medikaments (Investigational New Drug, IND) bei der US-amerikanischen Zulassungsbehörde FDA voraussichtlich in der zweiten Jahreshälfte 2024 und ein Testbeginn in den USA in der ersten Jahreshälfte 2025
    • Anhaltende Anerkennung und Aufmerksamkeit für Recce durch die kürzlich gehaltenen Referate bei der Biomedical Advanced Research and Development Authority (BARDA), die Eröffnungsrede und die F&E-Eröffnungsrede auf dem World AMR Congress 2024 und die Unterstützung der Regierungen von WA und NSW für die BIO International Convention 2024
    Avatar
    03.04.24 08:21:07
    Avatar
    14.12.23 10:30:46
    Avatar
    20.09.23 11:45:21
    Scheiben nicht viele mit zu bekommen, zumindest reagiert der Kurs noch nicht.

    Disclaimer