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NCT07214311 · Peptilogics

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)

What this study is about

The goal of this clinical trial is to evaluate whether the experimental 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).

View original scientific description

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.

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

Inclusion criteria

  • 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 criteria

  • 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)

Where

  • Sarasota, Florida
  • Tamarac, Florida
  • Baltimore, Maryland
  • Boston, Massachusetts
  • New York, New York
  • Leland, North Carolina
  • Cincinnati, Ohio
  • Cleveland, Ohio
  • Columbus, Ohio
  • Pittsburgh, Pennsylvania
  • Dallas, Texas
  • Edinburg, Texas

And 1 more location — see the full list below.

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Jul 2, 2026 · Source of record for eligibility and locations

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1 of 240 participants interested
0% interest

See if this study fits

A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

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Study locations

Choose your preferred location, or select flexible during enrollment.

RECRUITING

Sarasota

Florida

Location available
RECRUITING

Tamarac

Florida

Location available
RECRUITING

Baltimore

Maryland

Location available
RECRUITING

Boston

Massachusetts

Location available
RECRUITING

New York

New York

Location available
RECRUITING

Leland

North Carolina

Location available
RECRUITING

Cincinnati

Ohio

Location available
RECRUITING

Cleveland

Ohio

Location available
RECRUITING

Columbus

Ohio

Location available

And 4 more locations available.

Express your interest

Share your contact details and a study coordinator can follow up about screening.

Secure & Confidential

Your information is protected and will only be shared with the research team.

What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

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Looking for Prosthetic-joint Infection Treatment in Sarasota?

Join others in Florida exploring innovative treatment options through clinical research

Prosthetic-joint Infection Treatment Options in Sarasota, Florida

If you're searching for Prosthetic-joint Infection treatment in Sarasota, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Sarasota, Tamarac, Baltimore and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with Prosthetic-joint Infection. All study-related care is provided at no cost to participants.

Local Sites
3 locations in Florida
Now Enrolling
Up to 240 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for Prosthetic-joint Infection?

Potential Benefits

  • Access to new treatment approaches before public availability
  • Close monitoring by experienced medical professionals
  • Study-related care provided at no cost
  • Contribute to medical research for Prosthetic-joint Infection

What to Expect

  • Initial screening to determine eligibility
  • Regular check-ups and monitoring visits
  • Possible compensation for time and travel
  • You can withdraw at any time

Frequently Asked Questions About This Prosthetic-joint Infection Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT07214311. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.