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During a three-hour budget work session Thursday night, the Frederick County Board of Supervisors reached a consensus on funding for some outside agencies but delayed decisions for Laurel Ridge Community
Takeda has announced that the U.S. Food and Drug Administration (FDA) has approved a subcutaneous (SC) version of Entyvio, its treatment for adults with moderate to severe Crohn’s disease (CD).
Announced on April 18, the approval is based on the VISIBLE 2 trial and comes less than 7 months after the approval of SC vedolizumab in ulcerative colitis.
The approval was based on data from the phase 3 VISIBLE 2 trial.
The primary endpoint of the study was clinical remission at week 52 with vedolizumab