Clinical trial No longer in our active list Phase2; Phase3 Interventional Ages 50 and up

Evaluating Faricimab for treating eye diseases

Official title: Evaluation of Therapeutic Efficacy of Faricimab for Clinical AMD, DME, and RVO Patients

Run by Second Affiliated Hospital, School of Medicine, Zhejiang University · NCT06572553 · Data updated 2026-05-14

This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.

This study is testing if a new eye treatment called Faricimab can help adults with certain eye diseases, like age-related macular degeneration and diabetic macular edema, see better.

Quick facts

PhasePhase2; Phase3
Study typeInterventional
Ages50 Years and up
SexAll
Enrollment30 (estimated)
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University
Academic / other
Drugs / interventionsfaricimab
Locations1 site (Hanzhou, Zhejiang)
Trial IDNCT06572553 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include Chinese adults aged 18 and older diagnosed with nAMD, DME, or RVO.

Probably not a fit

Patients with active ocular inflammation, those receiving other anti-VEGF therapies, or unable to provide necessary clinical data may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial aims to assess the efficacy and safety of Faricimab in treating adults with neovascular age-related macular degeneration (nAMD), diabetic macular edema (DME), and retinal vein occlusion (RVO). Participants will receive monthly intravitreal injections of Faricimab for three months, with bi-weekly clinic visits for monitoring. The study focuses on improving visual acuity and understanding any medical issues related to the treatment. Faricimab is a bispecific antibody targeting both VEGF-A and Ang-2, potentially offering enhanced treatment outcomes for these retinal conditions.

Why it matters

Potential benefit: If successful, this treatment could significantly improve vision and quality of life for patients with these retinal diseases.

How similar studies have gone: Other studies have shown promise with similar dual-pathway approaches, indicating potential for success with Faricimab.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Chinese patients aged 18 years or older and of any gender;
2. Patients who have been diagnosed with nAMD, DME or RVO by OCT, FFA, ICGA or OCTA;
3. Patients whose decision to receive treatment with faricimab was made prior to and independent of study participation;
4. Patients who have received at least one treatment with faricimab during the course of the study;
5. have signed an informed consent form.

Exclusion Criteria:

1. Active ocular inflammation or suspected active ocular infection in either eye;
2. Receipt of any other anti-VEGF therapy after faricimab;
3. Patient is unable to provide clinical data (visual acuity and OCT images) within 2 weeks (14 days) prior to receiving the initial faricimab injection;
4. Currently participating in any other clinical trial.

Where it's running

  • 2 nd Affiliated Hospital, School of Medicine, Zhejiang University, China
    Hanzhou, Zhejiang, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.