Xbrane Working Towards Q2 2025 US Ranibizumab Approval

Plan Follows April CRL, Addition Of New US Marketing Partner

Xbrane plans to refile its proposed biosimilar to Lucentis by the end of 2024, after the recent disappointment of a US FDA complete response letter. However, the goal requires its manufacturing partners to successfully execute remediation plans.

Sprinter on starting blocks With 2025 text
• Source: Shutterstock

Xbrane Biopharma aims to resubmit its proposed US Xlucane (ranibizumab) biosimilar to Lucentis in the final three months of this year, potentially teeing up a BsUFA date and approval during the second quarter of 2025.

The Swedish developer has prioritized resubmission of its ranibizumab biosimilar since being hit with a US Food and Drug Administration...

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