Samsung Bioepis Reports Results of Post-Hoc Analysis from P-III Study of Byooviz (biosimilar- ranibizumab) for the Treatment of nAMD
- The P-III study evaluates Byooviz (0.5 mg- IVT) vs ranibizumab in 634 patients with nAMD. The results will be presented at EURETINA 2021
- The 1EPs are changed from baseline in BCVA @8wks. and change in CST @4wks. with both EPs- followed by 52wks. The post-hoc analysis showed that the baseline age- BCVA- CST- and total lesion size were identified to be associated with the visual acuity & anatomical outcomes
- In subgroup analysis- similar visual outcomes of 2 products in change from baseline in BCVA in multiple subgroups were observed & support an equivalent clinical efficacy. Byooviz is an effective & valuable treatment option for nAMD patients globally
| Ref: Samsung Bioepis | Image: Samsung Bioepis
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