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KESIMPTA is only indicated for the treatment of relapsing forms of MS, to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults 1 3

Unless there is clear evidence of primary bladder pathology (e.g., small capacity under anesthesia, Hunner lesions), patients should have a multidisciplinary evaluation including assessment for neuropathic pain and psychological profile

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Its approval means it has undergone Phase 3 clinical trials, FDA safety review, and ongoing post-market surveillance

Other animal wound-model work has been more mixed, including a report of slower reorganization and delayed fibroblast activation