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Xbrane publishes answers to questions received in recent days.

Following the communication regarding the delay in FDA approval for Lucamzi (Ximluci in the U.S.) and the Q3 report, Xbrane has received numerous questions. As many stakeholders have raised similar concerns, we have done our best to address these questions in the attached document.

Datum 2025-10-28, kl 21:00
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