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Vedolizumab (Entyvio) SC Approved for Maintenance Therapy in Adults with Moderately to Severely Active Crohn Disease
Vedolizumab for subcutaneous injection in now indicated for maintenance therapy following IV induction in both Crohn disease and ulcerative colitis.
Vedolizumab (Entyvio; Takeda) subcutaneous (SC) injection has earned FDA approval for maintenance therapy in adults with moderately to severely active Crohn disease after they have completed intravenous induction therapy with the biologic, according to an announcement from Takeda.1
This approval in Crohn disease follows the September 2023 approval of the gut-selective alpha4beta7 integrin inhibitor via subcutaneous administration for the same maintenance indication in adults with moderately to severely active ulcerative colitis.1
The IV formulation of vedolizumab was first approved by the FDA in 2014 for adults with moderate to severe ulcerative colitis and Crohn disease who had an inadequate or loss of response to or could not tolerate at least one previous treatment with corticosteroids, immunomodulators, or tumor necrosis factor blockers.2
The approval of vedolizumab SC was based on the phase 3 randomized, double-blind placebo-controlled VISIBLE 2 trial, which enrolled 409 adults with moderately to severely active Crohn disease who had had clinical response to vedolizumab IV by study week 6 after receiving 2 doses of open label IV vedolizumab at baseline and week 2.1
At the 6-week mark, the 409 participants were randomly assigned to receive the biologic agent or placebo via SC injection every 2 weeks. The VISIBLE 2 primary endpoint was clinical remission at study week 52, defined as total Crohn Disease Activity Index (CDAI) score of 150 or less.1
Among the study participants who received SC vedolizumab, nearly half (48%) reached long-term clinical remission after 52 weeks of treatment compared with approximately one-third (34%) of those who received placebo (P <.01), according to the company statement.1 The safety evaluation determined the SC vedolizumab profile is generally consistent with the known safety profile of the IV formulation, but also included local injection site reactions (ie, injection-site erythema, rash, pruritus, swelling, bruising, hematoma, pain, urticaria, and edema), Takeda said.1
“Crohn’s disease is a complex and usually progressive disease for which an appropriate management plan is critical. My primary goal as a clinician is always to get patients to achieve remission,” Timothy Ritter, MD, senior medical director, Department of Research and Education, GI Alliance Research and assistant professor of medicine, TCU School of Medicine, said in the Takeda statement.1 “In VISIBLE 2, about half of patients treated with Entyvio SC achieved long-term clinical remission.” Ritter added that the VISIBLE 2 outcomes “reaffirm the well-established efficacy profile of Entyvio, regardless of route of administration.”1
According to the Centers for Disease Control and Prevention, approximately 3.1 million adults in the US have been diagnosed with inflammatory bowel disease, comprised of Crohn disease and ulcerative colitis.3 There are significant differences in prevalence of the disease among racial and ethnic groups, according to new findings from the Crohn’s & Colitis Foundation. The organization’s study found that among White Americans, the rate of IBD is 7 times higher among than among Black Americans, 6 times higher than among Hispanic Americans, and 21 times higher than among Asian Americans.4
