China Faricimab Real World Evidence: Evaluation of Faricimab Effectiveness, Safety and Treatment Pattern, in Diabetic Macular Edema, Retinal Vein Occlusion and Neovascular Age-Related Macular Degeneration: The Farseeing Study

Status: Recruiting
Location: See all (6) locations...
Intervention Type: Drug
Study Type: Observational
SUMMARY

The Farseeing Study will explore long-term effectiveness, safety, and treatment patterns among patients being treated with faricimab in real-world, routine clinical practice in China. It is a primary data collection, non-interventional, prospective and retrospective, multi-center study designed to collect real-world, long-term data to gain clinical evidence on faricimab, by observing cohorts of patients with neovascular age-related macular degeneration (nAMD), diabetic macular edema (DME), and retinal vein occlusion (RVO) who are receiving treatment with faricimab.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Have signed the informed consent

• Female and male Chinese patients, who had been diagnosed with nAMD, DME, or RVO by CFP, OCT, FFA, ICGA, or OCTA

• ≥50 years old for patients with nAMD, ≥18 years old both for patients with DME and RVO, at the time of signing informed consent (or the first administration of faricimab, whichever occurs first)

• Patients for whom the decision to receive treatment with faricimab is made prior to and independent from study participation

• Patients have received at least one faricimab treatment (the first dose) in the study eye

Locations
Other Locations
China
Qingdao Eye Hospital of Shandong First Medical University
RECRUITING
Qingdao
Shanghai General Hospital
RECRUITING
Shanghai
Affiliated Hospital of Shandong Second Medical University
RECRUITING
Weifang
Tongji Hospital Tongji Medical College Huazhong University of Science and Technology
RECRUITING
Wuhan
Xiehe Hospital, Tongji Medical College Huazhong University of Science & Technology
RECRUITING
Wuhan
Hebei Eye Hospital
RECRUITING
Xingtai
Contact Information
Primary
Reference Study ID Number: ML45401 https://forpatients.roche.com/
global-roche-genentech-trials@gene.com
888-662-6728 (U.S. Only)
Time Frame
Start Date: 2024-05-09
Estimated Completion Date: 2027-11-30
Participants
Target number of participants: 1000
Treatments
Cohort 1: Patients with nAMD
Cohort 2: Patients with DME
Cohort 3: Patients with RVO
Sponsors
Collaborators: Shanghai Roche Pharmaceutical Co., Ltd
Leads: Hoffmann-La Roche

This content was sourced from clinicaltrials.gov