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Multi-center Real-world Study on Safety, Efficacy and Economy of Ranibizumab Biosimilars in Different Treatment Courses

Multi-center Real-world Study on Safety, Efficacy and Economy of Ranibizumab Biosimilars in Different Treatment Courses

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116694
Enrollment
Unknown
Registered
2026-01-14
Start date
2026-01-15
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ocular fundus diseases such as diabetic macular edema (DME), retinal vein occlusion (RVO), and neovascular age-related macular degeneration (nAMD)

Interventions

Observation Group:None

Sponsors

The First People's Hospital of Xuzhou
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Only patients who meet all the following inclusion criteria will be eligible for data collection in this study: 1. Patients have signed the informed consent form, volunteered to participate in this study, and have the willingness and ability to cooperate with data collection herein. 2. Patients have a clinical diagnosis of ocular fundus diseases such as diabetic macular edema (DME), retinal vein occlusion (RVO), and neovascular age-related macular degeneration (nAMD); 3. A prescription for the biosimilar ranibizumab was issued at the time of enrollment in the study. (The decision to prescribe the biosimilar ranibizumab shall be made by the attending physician and shall not be influenced by this study.)

Exclusion criteria

Exclusion criteria: Patients who meet any of the following criteria are prohibited from being enrolled in this study: The patient is undergoing or planning to participate in other clinical interventional studies. The patient is unable to understand the nature of this study or has not provided informed consent. The investigator determines that the patient is otherwise unsuitable for enrollment in the study.

Design outcomes

Primary

MeasureTime frame
Safety;

Secondary

MeasureTime frame
Changes in BCVA (Best-Corrected Visual Acuity) before and after treatment;Changes in CST (Central Subfield Thickness) before and after treatment;Economy;

Countries

China

Contacts

Public ContactLi Suyan

The First People's Hospital of Xuzhou

lisuyan1226@126.com+86 138 5210 1775

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026