May 2026 Johnson & Johnson received U.S. FDA approval for a supplemental Biologics License Application to update the TREMFYA (guselkumab) label with evidence demonstrating inhibition of structural joint damage progression in adults with active psoriatic arthritis, expanding its approved clinical benefits.
May 2026 Bristol Myers Squibb received European Commission approval for Sotyktu (deucravacitinib) for the treatment of adults with active psoriatic arthritis who have had an inadequate response or intolerance to prior disease-modifying antirheumatic drug therapy, marking the first TYK2 inhibitor approved for this indication in the EU.
March 2026 Bristol Myers Squibb received U.S. FDA approval for Sotyktu (deucravacitinib) for the treatment of adults with active psoriatic arthritis, expanding its immunology portfolio with the first TYK2 inhibitor approved for this indication.
March 2026 Sun Pharma announced that the U.S. FDA accepted the supplemental Biologics License Application for ILUMYA (tildrakizumab-asmn) for the treatment of adults with active psoriatic arthritis, advancing the regulatory pathway for a label expansion.