Patient Guide: Study to Evaluate the Efficacy and Safety of TRL1068 for the Treatment of Prosthetic Joint Infection

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 17 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06621251
Status: 🟢 Enrolling Now
Condition: Prosthetic Joint Infections of Hip, Prosthetic Joint Infections of Knee
Phase: PHASE2

Where You Can Participate

This study is available at 17 locations across the country.

Top locations include:
  • • Gilbert, Arizona
  • • Little Rock, Arkansas
  • • Los Angeles, California
  • • And 14 more locations

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Study to Evaluate the Efficacy and Safety of TRL1068 for the Treatment of Prosthetic Joint Infection - Join Clinical Trial NCTNCT06621251

How to Join This Clinical Trial - NCTNCT06621251

Learn how to participate in this PHASE2 trial studying an investigational therapy for Prosthetic Joint Infections of Hip, Prosthetic Joint Infections of Knee. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Prosthetic Joint Infections of Hip, Prosthetic Joint Infections of Knee. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Prosthetic Joint Infections of Hip, Prosthetic Joint Infections of Knee
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06621251 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 17 locations. Find a study site near you:

Clinical Research Site

Gilbert, Arizona 85234 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Little Rock, Arkansas 72205 - United States

Status: RECRUITING

Clinical Research Site

Los Angeles, California 90024 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Jacksonville, Florida 32224 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Sarasota, Florida 34232 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Tamarac, Florida 33321 - United States

Status: RECRUITING

Clinical Research Site

Baltimore, Maryland 21215 - United States

Status: RECRUITING

Clinical Research Site

Boston, Massachusetts 02120 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

New York, New York 10003 - United States

Status: RECRUITING

Clinical Research Site

Rochester, New York 14623 - United States

Status: RECRUITING

And 7 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2 clinical trial for Prosthetic Joint Infections of Hip, Prosthetic Joint Infections of Knee:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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