RecruitingPhase 2Phase 3NCT07214311

Evaluation of PLG0206 in Prevention of Recurrent Infection in Patients Undergoing Debridement, Antibiotics, and Implant Retention (DAIR) for Treatment of a Periprosthetic Joint Infection (PJI) Following Knee Arthroplasty

RETAIN: A Phase 2/3 Randomized, Placebo-Controlled Study to Evaluate the Efficacy of PLG0206 in Prevention of Recurrent Infection in Patients Undergoing Debridement, Antibiotics, and Implant Retention (DAIR) for Treatment of a Periprosthetic Joint Infection (PJI) Following Total Knee Arthroplasty (TKA)


Sponsor

Peptilogics

Enrollment

240 participants

Start Date

Feb 3, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to evaluate whether the investigational drug PLG0206 can help reduce recurrence of infection in adults who have undergone total knee replacement and are receiving a DAIR (Debridement, Antibiotics, and Implant Retention) surgical procedure to treat a Prosthetic Joint Infection (PJI). The study will also assess the safety of PLG0206 when used as an irrigation solution during the DAIR procedure. Participants will receive either PLG0206 or a placebo (an inactive substance that looks like the investigational drug), in addition to standard of care treatments. All participants will be monitored for approximately one year following their DAIR procedure.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Inclusion Criteria6

  • Male or female participants age between 18 and <80 years
  • Able to provide informed consent, geographically stable, and able to comply with the required follow-up visits
  • Suspected or confirmed PJI of the knee
  • Well-fixed and positioned prosthesis and good condition of surrounding soft tissue (no sinus tract)
  • A single DAIR procedure is indicated as treatment of PJI
  • Agree to use contraceptives if of childbearing potential

Exclusion Criteria9

  • Loose prosthesis or surgical treatment planned for removal of well-fixed, nonmodular implants
  • Anticipated to require antibiotic therapy for >6 months after DAIR procedure
  • Infection spread beyond the affected knee joint (e.g., osteomyelitis)
  • History of a prior PJI of the affected knee
  • Two or more prior revisions in the affected joint
  • Epithelialized sinus tract with evidence of communication to the joint or visualization of prosthesis
  • Diabetes mellitus and with an A1c ≥9%
  • History of malignant disease and having received immunosuppressive therapy, radiation therapy, or chemotherapy within the past year
  • Known immunodeficiency (e.g., splenectomy; sickle cell anemia; human immunodeficiency virus \[HIV\] with recent CD4 count <200 cells/mm3; or primary humoral, bone marrow, or other transplantation)

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Interventions

DRUGPLG0206

PLG0206 Solution

DRUGPlacebo

Placebo


Locations(8)

Clinical Trial Site

Sarasota, Florida, United States

Clinical Trial Site

Tamarac, Florida, United States

Clinical Trial Site

Baltimore, Maryland, United States

Clinical Trial Site

Boston, Massachusetts, United States

Clinical Trial Site

Cincinnati, Ohio, United States

Clinical Trial Site

Columbus, Ohio, United States

Clinical Trial Site

Pittsburgh, Pennsylvania, United States

Clinical Trial Site

Morgantown, West Virginia, United States

View Full Details on ClinicalTrials.gov

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NCT07214311


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