23 February 2023 | Thursday | News
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ALT-L9 Phase 3 trial (EudraCT: 2021-004530-11) is a randomized, double-masked, parallel group, multicenter study to compare the efficacy and safety of ALT-L9 versus Eylea® in 431 patients with wet AMD. Full recruitment of study volunteers refers to the 431st patient identified as an eligible subject and subsequently enrolled in the trial. In line with schedule set forth in trial protocol, study volunteers go through the process of investigational product administration and observation by investigators.
"Patient recruitment process has been further expedited as Altos Biologics closely communicated with trial collaborators at the local level," said an Alteogen official familiar with the study. "We plan to complete the product approval by the first half of 2025 as biologics license application (BLA) will be submitted to the relevant health authorities in early 2024. Altos Biologics is also making great strides in licensing-out efforts and companies possessing marketing capabilities and a proven track record would be prime candidates in forging partnerships."
The study builds upon earlier Phase 1 study (NCT: 04058535), which successfully demonstrated similar safety and efficacy profiles to the originator product and evaluated pharmacokinetic characteristics. Additionally, filing and registration of formulation patents related to higher thermal stability and process patents, enabling efficient drug substance manufacturing, further bolster the product's competitiveness from an intellectual property stance.
Eylea® is a leading treatment indicated for diabetic retinopathy and macular degeneration. In 2021 alone, the product clocked $5.8 billion in U.S. sales and worldwide, the revenue stood at $9.2 billion, making it one of the so-called blockbuster products. In an attempt to effectively capture Eylea® biosimilar market, Altos Biologics is pursuing licensing-out opportunities in each region.
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