Patient Guide: Real World Evidence in China: Faricimab Use in Diabetic Macular Edema, Retinal Vein Occlusion, and Neovascular Age-Related Macular Degeneration (The Farseeing Study)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 41 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06439576
Status: ACTIVE_NOT_RECRUITING
Condition: Diabetic Macular Edema, Neovascular Age-related Macular Degeneration, Retinal Vein Occlusion
Phase: Not Specified

Where You Can Participate

This study is available at 41 locations across the country.

Top locations include:
  • • Shantou, Guangdong
  • • Luoyang, Henan
  • • Shiyan, Hubei
  • • And 38 more locations

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Real World Evidence in China: Faricimab Use in Diabetic Macular Edema, Retinal Vein Occlusion, and Neovascular Age-Related Macular Degeneration (The Farseeing Study) - Join Clinical Trial NCTNCT06439576

How to Join This Clinical Trial - NCTNCT06439576

Learn how to participate in this Not Specified trial studying an investigational therapy for Diabetic Macular Edema, Neovascular Age-related Macular Degeneration, Retinal Vein Occlusion. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Diabetic Macular Edema, Neovascular Age-related Macular Degeneration, Retinal Vein Occlusion. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Diabetic Macular Edema, Neovascular Age-related Macular Degeneration, Retinal Vein Occlusion
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT06439576 - 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 41 locations. Find a study site near you:

Clinical Research Site

Shantou, Guangdong 515051 - China

Status: Contact for availability

Clinical Research Site

Luoyang, Henan 471000 - China

Status: Contact for availability

Clinical Research Site

Shiyan, Hubei 442000 - China

Status: Contact for availability

Clinical Research Site

Xuzhou, Jiangsu 221002 - China

Status: Contact for availability

Clinical Research Site

Fushun, Liaoning 110114 - China

Status: Contact for availability

Clinical Research Site

Panjin, Liaoning 124010 - China

Status: Contact for availability

Clinical Research Site

Shenyang, Liaoning 110001 - China

Status: Contact for availability

Clinical Research Site

Weifang, Shandong 261031 - China

Status: Contact for availability

Clinical Research Site

Shanghai, Shanghai Municipality 200080 - China

Status: Contact for availability

Clinical Research Site

Chengdu, Sichuan 610016 - China

Status: Contact for availability

And 31 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Diabetic Macular Edema, Neovascular Age-related Macular Degeneration, Retinal Vein Occlusion:

  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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