Amgen starts phase III trial for aflibercept biosimilar

Biosimilars/News | Posted 13/03/2020 post-comment0 Post your comment

US-based biotech giant Amgen is initiating a phase III clinical trial for a biosimilar of Regeneron’s Eylea (aflibercept).

Age-related macular degeneration V15b19

Aflibercept is a vascular endothelial growth factor (VEGF) inhibitor. It is indicated for the treatment of neovascular (wet) age-related macular degeneration, macular oedema following retinal vein occlusion, diabetic macular oedema and diabetic retinopathy in patients with diabetic macular oedema.

Amgen’s trial is a randomized, double-masked, 4-arm, phase III study of their candidate aflibercept biosimilar, ABP 938, versus Eylea. It will compare the efficacy and safety of the two products in subjects with neovascular age-related macular degeneration.

Amgen plans to enrol 566 participants at approximately 116 global sites. Subjects will be randomized in a masked 1:1 ratio to receive 2 mg (0.05 mL) of either ABP 938 (Treatment Group A) or Eylea (Treatment Group B) administered by intravitreal (IVT) injection.

The primary endpoint is the change in Best Corrected Visual Acuity (BCVA) as measured by Early Treatment Diabetic Retinopathy Study (ETDRS) letter score from baseline to Week 8. Secondary endpoints include change from baseline in BCVA, change from baseline in ETDRS letter score at Week 8 and Week 52, change from baseline in Choroidal Neovascularization (CNV) area, change from baseline in Central Subfield Thickness (CST) and number of subjects with incidence of anti-drug antibodies (ADA).

The study will last for a total of 56 weeks for each subject and is expected to be completed in April 2022.

Amgen is not the only one pursuing an aflibercept biosmilar. South Korean biologicals company Alteogen started a phase I trial for its candidate aflibercept biosimilar ALT-L9 in 2019 [1]. Momenta, who is developing an aflibercept biosimilar candidate, M710, with Mylan, is carrying out a ‘pivotal clinical trial’ and ‘expects to target US jointly developing an aflibercept biosimilar, FYB203 [2]. US-based Coherus BioSciences is expected to initiate phase III clinical trials for its aflibercept biosimilar candidate, CHS-2020, in 2021 with launch projected in 2025.

Related articles
Alteogen gains approval to start aflibercept biosimilar trial in Korea

Alteogen wins process patent for aflibercept biosimilar

References
1. GaBI Online - Generics and Biosimilars Initiative. Phase I trials started for aflibercept and ustekinumab biosimilars [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2020 Mar 13]. Available from: www.gabionline.net/Biosimilars/News/Phase-I-trials-started-for-aflibercept-and-ustekinumab-biosimilars
2. GaBI Online - Generics and Biosimilars Initiative. Mylan/Momenta announce development strategy for aflibercept biosimilar [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2020 Mar 13]. Available from: www.gabionline.net/Biosimilars/General/Mylan-Momenta-announce-development-strategy-for-aflibercept-biosimilar

Permission granted to reproduce for personal and non-commercial use only. All other reproduction, copy or reprinting of all or part of any ‘Content’ found on this website is strictly prohibited without the prior consent of the publisher. Contact the publisher to obtain permission before redistributing.

Copyright – Unless otherwise stated all contents of this website are © 2020 Pro Pharma Communications International. All Rights Reserved.

Source: clinicaltrials.gov

comment icon Comments (0)
Post your comment
Related content
FDA approves filgrastim biosimilar Nypozi
Filgrastim Grastofil V13H23
Biosimilars/News Posted 04/09/2024
FDA approves third aflibercept biosimilar Ahzantive
Bevacizumab VEGF Lucentis V21D02MN
Biosimilars/News Posted 13/08/2024
China approves Simcare’s cetuximab beta Enlituo
Cancer Cell V13I20
Biosimilars/News Posted 30/07/2024
Most viewed articles
About GaBI
Home/About GaBI Posted 06/08/2009
EU guidelines for biosimilars
EMA logo 1 V13C15
Home/Guidelines Posted 08/10/2010