*Figures in parentheses refer to the corresponding period of the previous year.

SIGNIFICANT EVENTS DURING
THE FIRST QUARTER 2026
• On March 31, Xbrane released a revised timeline for resubmission of the BLA application for its ranibizumab biosimilar to the U.S. Food and Drug Administration (FDA). It is estimated that the ap plication can be resubmitted in April–May 2026, when the contract manufacturer is expected to have completed all outstanding tasks associated with a previous Complete Response Letter (CRL). The processing time at the agency is then esti mated to be six months.

SIGNIFICANT EVENTS
AFTER THE END OF THE QUARTER
• In April, the company announced that it had resubmitted its Biologics License Application (BLA) to the U.S. Food and Drug Administra tion for its biosimilar candidate to Lucentis® (ranibizumab).
• In May, the Company announced that it had revised the agreement with its collaboration partner Intas, whereby Intas will assume f inancing of certain CMC-related develop ment activities. The agreement entails that all costs financed by Intas, including an accumulated markup of 18% per annum, will be deducted from future profit-sharing payments. Intas is also granted the option, instead of profit sharing, to elect a lump-sum payment equivalent to 40 months of forecast profit sharing. Otherwise, Xbrane’s and Intas’s respective commitments remain unchanged in accordance with the original license agreement.

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Q1 Report 2026