Patient Guide: A Study to Evaluate AZD7760 Safety and Pharmacokinetics in Healthy Adults (Phase I) and Adults With End-stage Kidney Disease on Hemodialysis With a Central Venous Catheter (Phase IIa)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 40 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06749457
Status: 🟢 Enrolling Now
Condition: Staphylococcus Aureus
Phase: PHASE1, PHASE2

Where You Can Participate

This study is available at 40 locations across the country.

Top locations include:
  • • Huntsville, Alabama
  • • Glendale, California
  • • Granada Hills, California
  • • And 37 more locations

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A Study to Evaluate AZD7760 Safety and Pharmacokinetics in Healthy Adults (Phase I) and Adults With End-stage Kidney Disease on Hemodialysis With a Central Venous Catheter (Phase IIa) - Join Clinical Trial NCTNCT06749457

How to Join This Clinical Trial - NCTNCT06749457

Learn how to participate in this PHASE1, PHASE2 trial studying an investigational therapy for Staphylococcus Aureus. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Staphylococcus Aureus. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Staphylococcus Aureus
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1, PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06749457 - 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 40 locations. Find a study site near you:

Clinical Research Site

Huntsville, Alabama 35805 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Glendale, California 91206 - United States

Status: RECRUITING

Clinical Research Site

Granada Hills, California 91344 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

La Mesa, California 91942 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Los Angeles, California 90027 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Northridge, California 91324 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Northridge, California 91325 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Oxnard, California 93036 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Riverside, California 92503 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

San Dimas, California 91773 - United States

Status: RECRUITING

And 30 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE1, PHASE2 clinical trial for Staphylococcus Aureus:

  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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