New antibiotic zoliflodacin targets drug-resistant gonorrhoea

A new oral antibiotic called zoliflodacin has shown effectiveness in treating gonorrhoea, clearing 91 percent of infections in a clinical trial. The drug offers a potential alternative to the increasingly resistant standard treatment of ceftriaxone. With resistance to existing antibiotics rising globally, this development could help delay the emergence of untreatable strains.

Gonorrhoea, caused by the bacterium Neisseria gonorrhoeae, infects more than 80 million people worldwide each year. The infection, which spreads through sexual contact, often leads to symptoms like burning during urination and abnormal discharge from the genitals. Untreated cases can result in infertility and complications during pregnancy.

Standard treatment relies on injectable ceftriaxone, but resistance is growing. According to the World Health Organization, about 5 percent of cases in 12 countries—including Thailand, South Africa, and Brazil—were resistant to ceftriaxone in 2024, a sixfold rise from 2022. "We are running out of options," noted Alison Luckey from the Global Antibiotic Research and Development Partnership, highlighting the decades-long gap since the last new gonorrhoea drug approval.

To address this, researchers tested zoliflodacin on 744 patients across the US, South Africa, Thailand, Belgium, and the Netherlands. Participants received either zoliflodacin or the standard combination of ceftriaxone and azithromycin. After six days, swabs showed zoliflodacin cleared 91 percent of infections, compared to 96 percent for the standard therapy—a difference deemed insignificant. Both treatments caused similar mild, temporary side effects like headaches and nausea.

While most trial cases involved non-resistant strains, lab tests confirm zoliflodacin works against bacteria resistant to all common antibiotics. As an oral option, it may appeal more than injections, which some avoid due to needle phobia. Luckey suggested its use as a first-line treatment in high-resistance areas.

The team has submitted data to the US Food and Drug Administration, expecting a decision on December 15. Approvals in the UK, Europe, and Asia could follow, per Charlotte-Eve Short of Imperial College London. Combined with the recent UK rollout of the meningitis B vaccine for gonorrhoea prevention, these advances—alongside the pending approval of gepotidacin—signal progress against antimicrobial resistance. "This is great news," Short said, emphasizing the dual approach of prevention and treatment.

Verwandte Artikel

Photorealistic image of zoliflodacin antibiotic pill next to The Lancet journal reporting successful phase 3 trial results for gonorrhea treatment.
Bild generiert von KI

Lancet reports phase 3 results for single-dose oral zoliflodacin in uncomplicated gonorrhea

Von KI berichtet Bild generiert von KI Fakten geprüft

Results from a global phase 3 trial of zoliflodacin, an investigational single-dose oral antibiotic, were published in The Lancet in December 2025, showing the drug was non-inferior to a ceftriaxone-based standard regimen for curing uncomplicated urogenital gonorrhea in a study of 930 participants across five countries.

Da Antibiotika zunehmend versagen, führen Forscher am AIIMS Delhi den Kampf gegen Superbakterien durch frühe Diagnose, Biomarker-Forschung und rationalen Antibiotikaeinsatz. Ein kürzlicher Fall eines 50-jährigen Mannes mit resistenter bakterieller Meningitis unterstreicht die Dringlichkeit. Das Institut betreibt mehrere Projekte, um die antimikrobielle Resistenz zu verlangsamen.

Von KI berichtet

Scientists at the University of Basel have developed a novel testing method to determine whether antibiotics actually eliminate bacteria or merely halt their growth. This approach, called antimicrobial single-cell testing, tracks individual bacteria under a microscope to assess drug effectiveness more accurately. The findings, published in Nature Microbiology, highlight variations in bacterial tolerance to treatments for tuberculosis and other lung infections.

A nasal spray delivering a broad-spectrum antibody has demonstrated potential to prevent infections from any flu strain in animal and preliminary human studies. Developed initially by Johnson & Johnson and now advanced by Leyden Labs, the spray could offer rapid protection during pandemics. Experts see it as a valuable tool for high-risk groups, though further testing is needed.

Von KI berichtet

Das Pharmaunternehmen Gilead Sciences hat ein Memorandum of Understanding mit Farmanguinhos, einem Teil von Fiocruz, unterzeichnet, um Technologietransfer und lokale Produktion von Lenacapavir, einer semestrialen HIV-Präventionsinjektion, zu prüfen. Das Abkommen soll Kosten senken und die Zugänglichkeit in Brasilien verbessern, ist jedoch noch kein formelles Engagement. Anvisa hat das Medikament am 12. Januar 2026 genehmigt.

Die brasilianische nationalen Agentur für Gesundheitsaufsicht (Anvisa) hat Lenacapavir, vermarktet als Sunlenca, für die Verwendung als Präexpositionsprophylaxe (PrEP) gegen HIV-1 zugelassen. Das Medikament, das alle sechs Monate subkutan injiziert wird, zeigte in klinischen Studien mit vulnerablen Populationen eine Wirksamkeit von bis zu 100 %. Die Zulassung ebnet den Weg für regulatorische Schritte, die zu seiner Verfügbarkeit im Einheitlichen Gesundheitssystem (SUS) führen könnten.

Von KI berichtet

Die stellvertretende Gesundheitsministerin Kenias Mary Muthoni hat die Bürger aufgefordert, Antibiotika ohne ärztliches Rezept nicht zu kaufen, insbesondere während der Festtagszeit, wenn Symptome wie Durchfall und Erbrechen häufig sind.

 

 

 

Diese Website verwendet Cookies

Wir verwenden Cookies für Analysen, um unsere Website zu verbessern. Lesen Sie unsere Datenschutzrichtlinie für weitere Informationen.
Ablehnen