Patient Guide: A Study to Investigate the Effects of Zibotentan/Dapagliflozin Combination Compared to Dapagliflozin Alone in Adult Participants With Chronic Kidney Disease and High Proteinuria

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 10 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06942910
Status: 🟢 Enrolling Now
Condition: Chronic Kidney Disease With High Proteinuria
Phase: PHASE2

Where You Can Participate

This study is available at 10 locations across the country.

Top locations include:
  • • Aramil,
  • • Izhevsk,
  • • Moscow,
  • • And 7 more locations

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A Study to Investigate the Effects of Zibotentan/Dapagliflozin Combination Compared to Dapagliflozin Alone in Adult Participants With Chronic Kidney Disease and High Proteinuria - Join Clinical Trial NCTNCT06942910

How to Join This Clinical Trial - NCTNCT06942910

Learn how to participate in this PHASE2 trial studying an investigational therapy for Chronic Kidney Disease With High Proteinuria. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Chronic Kidney Disease With High Proteinuria. 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 With High Proteinuria
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06942910 - 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 10 locations. Find a study site near you:

Clinical Research Site

Aramil, 624002 - Russian Federation

Status: RECRUITING

Clinical Research Site

Izhevsk, 426061 - Russian Federation

Status: SUSPENDED

Clinical Research Site

Moscow, 111539 - Russian Federation

Status: RECRUITING

Clinical Research Site

Moscow, 117036 - Russian Federation

Status: RECRUITING

Clinical Research Site

Moscow, 129327 - Russian Federation

Status: RECRUITING

Clinical Research Site

Perm, 614000 - Russian Federation

Status: RECRUITING

Clinical Research Site

Saratov, 410053 - Russian Federation

Status: RECRUITING

Clinical Research Site

Saratov, 410054 - Russian Federation

Status: RECRUITING

Clinical Research Site

St Petersburg, 195067 - Russian Federation

Status: RECRUITING

Clinical Research Site

Yaroslavl, 150062 - Russian Federation

Status: RECRUITING

How to Enroll in This Study

To learn more about participating in this PHASE2 clinical trial for Chronic Kidney Disease With High Proteinuria:

  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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