Patient Guide: A Study to Learn How Well the Study Treatment Finerenone Works and How Safe it is in People With Long-term Decrease in the Kidneys' Ability to Work Properly (Chronic Kidney Disease) Together With Type 1 Diabetes

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 80 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05901831
Status: ACTIVE_NOT_RECRUITING
Condition: Chronic Kidney Disease, Type 1 Diabetes Mellitus
Phase: PHASE3

Where You Can Participate

This study is available at 80 locations across the country.

Top locations include:
  • • Surprise, Arizona
  • • Stanford, California
  • • Vallejo, California
  • • And 77 more locations

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A Study to Learn How Well the Study Treatment Finerenone Works and How Safe it is in People With Long-term Decrease in the Kidneys' Ability to Work Properly (Chronic Kidney Disease) Together With Type 1 Diabetes - Join Clinical Trial NCTNCT05901831

How to Join This Clinical Trial - NCTNCT05901831

Learn how to participate in this PHASE3 trial studying an investigational therapy for Chronic Kidney Disease, Type 1 Diabetes Mellitus. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Chronic Kidney Disease, Type 1 Diabetes Mellitus. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Chronic Kidney Disease, Type 1 Diabetes Mellitus
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05901831 - 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 80 locations. Find a study site near you:

Clinical Research Site

Surprise, Arizona 85374 - United States

Status: Contact for availability

Clinical Research Site

Stanford, California 94305 - United States

Status: Contact for availability

Clinical Research Site

Vallejo, California 94592 - United States

Status: Contact for availability

Clinical Research Site

Miami, Florida 33136-1013 - United States

Status: Contact for availability

Clinical Research Site

Orlando, Florida 32804 - United States

Status: Contact for availability

Clinical Research Site

Orlando, Florida 32806 - United States

Status: Contact for availability

Clinical Research Site

Port Charlotte, Florida 33952 - United States

Status: Contact for availability

Clinical Research Site

Tampa, Florida 33619 - United States

Status: Contact for availability

Clinical Research Site

West Palm Beach, Florida 33401 - United States

Status: Contact for availability

Clinical Research Site

Atlanta, Georgia 30303 - United States

Status: Contact for availability

And 70 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Chronic Kidney Disease, Type 1 Diabetes Mellitus:

  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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