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Bimekizumab response maintenance to 48 weeks in patients with moderate to severe hidradenitis suppurativa: Pooled responder analysis from the phase 3, double-blind, placebo-controlled, randomized clinical trials BE HEARD I & II

Important Information Related to Your Request:

The material below is provided in response to your specific search for information on UCBCOMPASS® and may contain information that is not part of the FDA-approved Prescribing Information. UCB, Inc. does not recommend or endorse the use of its products in a manner not consistent with the approved Prescribing Information. Please review the Full Prescribing Information.

The safety and efficacy of bimekizumab in hidradenitis suppurativa (HS) have not been established and it is not approved for use in HS by any regulatory authority worldwide.  The material below is provided in response to your specific search for information on UCBCOMPASS®.  It is not intended to draw any conclusion regarding the efficacy and safety of bimekizumab for any indication, dosage, or other claim.

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