CELLDEX (CLDX) Phase 3 Trials of Barzolvolimab Hit All Endpoints in Hives

Both EMBARQ-CSU studies met their primary and all key secondary endpoints, with complete response rates above 42% at 12 weeks; BLA planned for 2027.

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Barzolvolimab is being developed for chronic spontaneous urticaria, a condition marked by persistent hives and itch.

Celldex Therapeutics (CLDX) reported positive topline results from its two pivotal Phase 3 trials of barzolvolimab in chronic spontaneous urticaria, with both EMBARQ-CSU1 and EMBARQ-CSU2 meeting the primary endpoint and all key secondary endpoints at 12 weeks across both dose groups. The company said it intends to file a Biologics License Application with the FDA in 2027.