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Obexelimab met the primary endpoint, reducing IgG4-RD flare risk by 56%, and all four key secondary efficacy endpoints. It was well tolerated with no new safety signals. Zenas plans to submit a Biologics License Application to the FDA in Q2 2026 and a Marketing Authorization Application to the EMA in H2 2026. The company will host a conference call today at 8:00 a.m. ET.
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