Patient Guide: A Study of Tirzepatide (LY3298176) in Participants With Overweight or Obesity and Chronic Kidney Disease With or Without Type 2 Diabetes

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 27 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05536804
Status: ACTIVE_NOT_RECRUITING
Condition: Overweight, Obesity, Chronic Kidney Disease, Type 2 Diabetes, T2D
Phase: PHASE2

Where You Can Participate

This study is available at 27 locations across the country.

Top locations include:
  • • Northridge, California
  • • Aurora, Colorado
  • • Denver, Colorado
  • • And 24 more locations

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A Study of Tirzepatide (LY3298176) in Participants With Overweight or Obesity and Chronic Kidney Disease With or Without Type 2 Diabetes - Join Clinical Trial NCTNCT05536804

How to Join This Clinical Trial - NCTNCT05536804

Learn how to participate in this PHASE2 trial studying an investigational therapy for Overweight, Obesity, Chronic Kidney Disease, Type 2 Diabetes, T2D. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Overweight, Obesity, Chronic Kidney Disease, Type 2 Diabetes, T2D. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Overweight, Obesity, Chronic Kidney Disease, Type 2 Diabetes, T2D
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05536804 - 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 27 locations. Find a study site near you:

Clinical Research Site

Northridge, California 91325 - United States

Status: Contact for availability

Clinical Research Site

Aurora, Colorado 80045 - United States

Status: Contact for availability

Clinical Research Site

Denver, Colorado 80210 - United States

Status: Contact for availability

Clinical Research Site

Avon, Indiana 46123 - United States

Status: Contact for availability

Clinical Research Site

Greenfield, Indiana 46140 - United States

Status: Contact for availability

Clinical Research Site

Indianapolis, Indiana 46202 - United States

Status: Contact for availability

Clinical Research Site

Muncie, Indiana 47304 - United States

Status: Contact for availability

Clinical Research Site

Troy, Michigan 48098 - United States

Status: Contact for availability

Clinical Research Site

Seattle, Washington 98195 - United States

Status: Contact for availability

Clinical Research Site

Spokane, Washington 99204 - United States

Status: Contact for availability

And 17 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 Overweight, Obesity, Chronic Kidney Disease, Type 2 Diabetes, T2D:

  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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