This study focuses on patients with prosthetic joint infection in the hip or knee caused by Staphylococcus aureus bacteria. The infection occurs around artificial joint implants and requires medical intervention. The study evaluates a new treatment approach using bacteriophages (viruses that target specific bacteria) in combination with a standard surgical procedure called DAIR (debridement, antibiotics, and implant retention).
The treatment being tested includes two investigational products, PP1493 and PP1815, which are bacteriophage solutions given through intra-articular injection (injection directly into the joint). These will be compared to a placebo treatment, with both groups also receiving standard surgical care. The study aims to determine if adding bacteriophage therapy to standard treatment is safe and effective for treating prosthetic joint infections.
The study will monitor patients for three months to assess their response to treatment. Participants will receive either the bacteriophage treatment or placebo, along with standard care. During the study, doctors will track the healing of the infection and monitor for any side effects. The treatment period lasts for three days, with follow-up evaluations continuing for several months to ensure patient safety and assess treatment effectiveness.



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