A Phase II Proof of Concept Multicenter, Randomized, Double-Blind Study to Assess the Safety and Efficacy of Phage Therapy in Patients With Hip or Knee Prosthetic Joint Infection Due to Staphylococcus Aureus Treated by DAIR
Overview
- Phase
- Phase 2
- Intervention
- Anti-Staphylococcus aureus Bacteriophages (PP1493 and PP1815) intra-articular injection with 0.9% NaCl solution
- Conditions
- Hip Prosthesis Infection
- Sponsor
- Phagenix
- Enrollment
- 100
- Locations
- 10
- Primary Endpoint
- To assess the safety of phage therapy + DAIR compared with placebo + DAIR
- Status
- Not yet recruiting
- Last Updated
- 26 days ago
Overview
Brief Summary
Total joint replacements are effective for chronic pain but can lead to Prosthetic Joint Infections (PJI), primarily caused by Staphylococcus aureus and resistant to antibiotics. Standard treatment involves DAIR surgery and antibiotics, but there's a need for better solutions due to rising infections and antibiotic resistance. Bacteriophage therapy, which targets specific bacteria, shows promise. Phaxiam Therapeutics is studying the safety and efficacy of phage therapy in treating Staphylococcus aureus infections in hip or knee PJI patients undergoing DAIR.
Detailed Description
Total joint replacement serves as valuable interventions in the management of chronic refractory pain when the other conservative treatments have not worked. They play a vital role in alleviating discomfort and improving the quality of life of subjects battling with joint diseases. However, the joint replacements present the challenge of Prosthetic Joint Infection (PJI). PJI have serious complications and can lead to significant mortality, morbidity, and healthcare expenditure. The leading cause of PJI is gram-positive cocci, specifically Staphylococcus aureus. Bacterial biofilms, mainly formed with Staphylococcus, represent a significant challenge in the treatment of PJIs due to their resistance to antibiotic therapy. Standard of Care (SOC) for these complex infections is characterized primarily by an initial surgery (Debridment Antibiotics and Implant Retention (DAIR) and various regiments and combinations of antibiotics. While the patterns of utilization vary between institutions and geography, DAIR is considered low-invasive procedure, characterized by the possibility of not explanting the prosthetic implant and resecting the bone. The growing demand for joint arthroplasty and current PJI rates, combined with antibacterial resistance, clearly indicate an unmet medical need in treating biofilm-based PJIs. Bacteriophage therapy could potentially improve the treatment paradigm for PJIs. Bacteriophages naturally occur with highly specific bacterial viruses that infiltrate bacterial cells, disrupting their metabolism, and causing bacterial lysis. Initial in vivo studies of phage therapy for bone-related infections have shown promise. Phaxiam Therapeutics, a biotechnology company specializing in the research and development of anti-infective therapies using bacteriophages., has collections of phages against Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus. These phages have shown promise in preliminary tests and studies. The objective of GLORIA study Is to assess the safety and efficacy of phage therapy versus placebo in treating Staphylococcus aureus infections in hip or knee PJI patients undergoing DAIR.
Investigators
Chief Medical Officer
Scientific
Phaxiam Therapeutics
Eligibility Criteria
Inclusion Criteria
- •Male or female ≥ 18 years
- •Knee or Hip PJI according to EBJIS (European Bone and Joint Infection) or ICM (International Consensus Meeting) guidelines
- •Monobacterial Infection due to S. aureus
- •Without preoperative diagnosis of superinfection due to another pathogen if treatment is administered at the end of the DAIR (presence of a contaminant is not considered clinically relevant)
- •Without diagnosis of superinfection due to another pathogen identified within 72h after bacteriological sample performed during the DAIR if treatment is administered up to 14 days after the DAIR
- •Indication for Open DAIR decided by the Multidisciplinary Team and/or Principal Investigator
- •S. aureus in joint fluid during the pre-inclusion period or in case of relapse of infection under antibiotics therapy in the last 6 months before inclusion
- •Patient with a life expectancy of 1 year or more as determined by the principal investigator.
- •Females of childbearing potential/Sexually active males with partner of childbearing potential: commitment to consistently and correctly use an acceptable effective method of birth control until 1 month after the last study drug administration.
- •Females of non-childbearing potential: either surgically sterilized or at least 1 year postmenopausal (amenorrhea duration at least 12 months)
Exclusion Criteria
- •Relapse between DAIR and study drug administration planned up to 14 days after the DAIR.
- •Patients who have two planned DAIR in sequence (double DAIR)
- •Patients with ASA score ≥ 4
- •Severe sepsis or Septic shock or hemodynamic instability
- •Patients with an indication for fixed prosthesis exchange, or for joint fusion or for amputation
- •Indication for suppressive antibiotherapy
- •Immunosuppressed patients: Patients having a weakened immune system due to diseases conditions (i.e. genetic disorders, malnutrition) or treatment (i.e. anticancer drugs or organ transplant)
- •Positive Human Immunodeficiency Viruses (HIV) test or active hepatitis B and C
- •Previous treatment by bacteriophages
- •Any known phage allergy and/or to its excipients
Arms & Interventions
Active Arm
Anti-Staphylococcus aureus Bacteriophages (PP1493 and PP1815) intra-articular injection with 0.9% NaCl solution
Intervention: Anti-Staphylococcus aureus Bacteriophages (PP1493 and PP1815) intra-articular injection with 0.9% NaCl solution
Control Arm
0.9% NaCl solution
Intervention: 0.9% NaCl solution
Outcomes
Primary Outcomes
To assess the safety of phage therapy + DAIR compared with placebo + DAIR
Time Frame: From enrollment up to 3 months
Incidence of serious adverse events
To assess the efficacy of phage therapy + DAIR compared with placebo + DAIR
Time Frame: From enrollment up to 3 months
Percentage of patients with clinical cure
Incidence of serious adverse events up to 3 months
Incidence of serious adverse events up to 3 months
Percentage of Patients with clinical cure up to 3 months
Percentage of Patients with clinical cure up to 3 months
Secondary Outcomes
- To assess the safety of phage therapy + DAIR compared with placebo + DAIR(From enrollment up to 12 months)
- To assess the efficacy of phage therapy + DAIR compared with placebo + DAIR(From enrollment up to 12 months)
- To describe the immunological response in serum and in joint fluid(From enrollment up to 3 months)
- To describe the S. aureus bacterial load (bacteriology) in the joint fluid up to 1 month(From enrollment up to 1 month)
- To describe Cytology in the joint fluid(From enrollment up to 1 month)
- To describe the hospitalization duration(From enrollment up to 3 months and up to 12 months)
- To describe the quality of life for patients(From enrollment up to 3 months and up to 12 months)
- To describe joint function rehabilitation(From enrollment up to 3 months and up to 12 months)
- To describe the evolution of the prosthetic joint infection by X Ray image(From screening up to 3 months and up to 12 months)
- Percentage of patients with clinical cure from S.aureus infection up to 3 months and 12 months. Percentage of patients with relapse exclusively due to another germ than Staphylococcus aureus up to 3 month and 12 months
- Incidence of all adverse events and assessment of all safety parameters (Vital signs, ECG/ Echocardiography, hematology, hemostasis and biochemistry) up to 3 months and up to 12 months
- Percentage of Patient with clinical cure of PJI and up to 12 months.
- Titration of anti-S. aureus phage antibodies: -In [redacted] at [redacted] in case of relapse and at Early End Visit if it’s occurred before [redacted] for all patients. -In [redacted] at [redacted] in case of relapse if it’s occurred before [redacted] (all patient) and only for knee PJI patients at [redacted].
- Quantitative or Semi-Quantitative Analysis of bacterial load at [redacted] (all patient) and only for knee PJI patient at [redacted].
- Quantification and identification of polynuclear of [redacted] at [redacted] (all patients) and [redacted] (only knee PJI).
- Number and Duration of hospitalization up to 3 months and up to 12 months
- Quality-of-life questionnaires [redacted] at [redacted].
- [redacted] Questionnaires at [redacted].
- X Ray during [redacted] period and at [redacted] to check potential appearance of abnormal loosening (border with shifting of the prosthesis), periprosthetic border.