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FYB-201 Biosimilar ranibizumab (Ongavia/Ranivisio/Cimerli) Efficacy and Safety in Clinical Settings - FORCE study.

Publication ,  Journal Article
Sharma, A; Nicholson, L; Vazquez-Alfageme, C; Sivagnanavel, V; Fausto, R; Soare, MC; Salamanca, MB; Fabozzi, L; Tsika, C; Corbalan, OC; Woo, SJ ...
Published in: Eye (Lond)
December 2025

PURPOSE: To understand the early experience of ranibizumab biosimilar (FYB 201) that has been approved in the United Kingdom (Ongavia, Teva Pharmaceuticals, Tel Aviv Israel), United States (Cimerli, Sandoz Inc, Princeton, NJ, USA) and Europe (Ranivisio, Bioeq AG, Zug, Switzerland). METHODS: 1230 patients received 3595 ranibizumab biosimilar (FYB 201) injections for variable indications in this multicentric retrospective study. All patients were treated with at least one intravitreal injection of ranibizumab biosimilar (FYB 201) 0.5 mg. Primary outcome was best-corrected visual acuity (BCVA). Secondary outcome was central foveal thickness (CFT). Other outcome measures included adverse events. RESULTS: A total of 3595 ranibizumab biosimilar (FYB 201) injections were given for neovascular age-related macular degeneration (n-AMD) (n = 802), other causes of choroidal neovascularization (CNV) (n = 36), diabetic macular oedema (DMO) (n = 169), retinal vein occlusion (RVO) (n = 155), myopic macular neovascularisation (m-MNV) (n = 61), cystoid macular oedema (CMO) (n = 6) and proliferative diabetic retinopathy (n = 1). Mean age was 77.2 ± 12.7 years and 80.9% were females. The mean follow-up period was 15.7 ± 9.9 weeks after the first injection of ranibizumab biosimilar (FYB 201). Overall, the mean BCVA remained stable from 0.57 ± 0.21 at baseline to 0.56 ± 1.8 at the last follow-up (p = 0.84, 95% CI -0.0915 to 0.1115). The mean CFT was significantly reduced from 260.5 ± 141.8 μm at baseline to 211.4 ± 113.2 μm at the last follow-up (p = 0.0001, 95% CI 38.935 to 59.265). Three eyes (0.24%) had ocular adverse events and 6 patients (0.48%) experienced systemic adverse events during the study period. CONCLUSION: Ranibizumab biosimilar (FYB 201) injections were effective and safe in this real-world experience, with stable visual acuity and reduced CFT with no major complications.

Duke Scholars

Published In

Eye (Lond)

DOI

EISSN

1476-5454

Publication Date

December 2025

Volume

39

Issue

17

Start / End Page

3129 / 3134

Location

England

Related Subject Headings

  • Visual Acuity
  • Vascular Endothelial Growth Factor A
  • Treatment Outcome
  • Tomography, Optical Coherence
  • Retrospective Studies
  • Ranibizumab
  • Ophthalmology & Optometry
  • Middle Aged
  • Male
  • Macular Edema
 

Citation

APA
Chicago
ICMJE
MLA
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Sharma, A., Nicholson, L., Vazquez-Alfageme, C., Sivagnanavel, V., Fausto, R., Soare, M. C., … International Retina Biosimilar Study Group (Inter BIOS Group). (2025). FYB-201 Biosimilar ranibizumab (Ongavia/Ranivisio/Cimerli) Efficacy and Safety in Clinical Settings - FORCE study. Eye (Lond), 39(17), 3129–3134. https://doi.org/10.1038/s41433-025-04030-7
Sharma, Ashish, Luke Nicholson, Clara Vazquez-Alfageme, Vasuki Sivagnanavel, Riccardo Fausto, Maria Cristina Soare, Marta Bautista Salamanca, et al. “FYB-201 Biosimilar ranibizumab (Ongavia/Ranivisio/Cimerli) Efficacy and Safety in Clinical Settings - FORCE study.Eye (Lond) 39, no. 17 (December 2025): 3129–34. https://doi.org/10.1038/s41433-025-04030-7.
Sharma A, Nicholson L, Vazquez-Alfageme C, Sivagnanavel V, Fausto R, Soare MC, et al. FYB-201 Biosimilar ranibizumab (Ongavia/Ranivisio/Cimerli) Efficacy and Safety in Clinical Settings - FORCE study. Eye (Lond). 2025 Dec;39(17):3129–34.
Sharma, Ashish, et al. “FYB-201 Biosimilar ranibizumab (Ongavia/Ranivisio/Cimerli) Efficacy and Safety in Clinical Settings - FORCE study.Eye (Lond), vol. 39, no. 17, Dec. 2025, pp. 3129–34. Pubmed, doi:10.1038/s41433-025-04030-7.
Sharma A, Nicholson L, Vazquez-Alfageme C, Sivagnanavel V, Fausto R, Soare MC, Salamanca MB, Fabozzi L, Tsika C, Corbalan OC, Verdejo AG, Wakabayashi T, Woo SJ, Kolomeyer AM, Mansour H, Momenaei B, Regillo CD, International Retina Biosimilar Study Group (Inter BIOS Group). FYB-201 Biosimilar ranibizumab (Ongavia/Ranivisio/Cimerli) Efficacy and Safety in Clinical Settings - FORCE study. Eye (Lond). 2025 Dec;39(17):3129–3134.

Published In

Eye (Lond)

DOI

EISSN

1476-5454

Publication Date

December 2025

Volume

39

Issue

17

Start / End Page

3129 / 3134

Location

England

Related Subject Headings

  • Visual Acuity
  • Vascular Endothelial Growth Factor A
  • Treatment Outcome
  • Tomography, Optical Coherence
  • Retrospective Studies
  • Ranibizumab
  • Ophthalmology & Optometry
  • Middle Aged
  • Male
  • Macular Edema