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NCT04667910

601 Versus Ranibizumab in Patients With Central Retinal Vein Occlusion (CRVO)

Completed Phase 2 Last updated 27 June 2025
What this trial tests

Phase 2 trial testing 601 1.25mg in Central Retinal Vein Occlusion in 60 participants. Completed in 16 November 2022.

Timeline
27 January 2021
Primary endpoint
16 November 2022
16 November 2022

Quick facts

Lead sponsorSunshine Guojian Pharmaceutical (Shanghai) Co., Ltd.
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment60
Start date27 January 2021
Primary completion16 November 2022
Estimated completion16 November 2022
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd. — full company profile →

Who can join

18 and older, any sex, with Central Retinal Vein Occlusion. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To evaluate the safety and efficacy of intravitreal recombinant humanized anti-VEGF monoclonal antibody in patients with visual impairment due to macular edema secondary to CRVO

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Efficacy and safety of anti-VEGF monoclonal antibody 601 for macular oedema in retinal vein occlusion: two phase IIa randomised clinical trials.
    Zhao S, Wu M, Zhong J, Chen B, et al · · 2025 · PMID 41448868 · DOI 10.1136/bjo-2025-327845

Verify or expand the search:

Other trials of 601 1.25mg

Trials testing the same drug.

Other recruiting trials for Central Retinal Vein Occlusion

Currently open trials in the same condition.

Other Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd. trials

Trials by the same sponsor.

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Data sources for this page

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