
The new approval is backed by ADAPT SERON results showing significant MG-ADL improvement and consistent safety.

The new approval is backed by ADAPT SERON results showing significant MG-ADL improvement and consistent safety.

The FDA approved anifrolumab via a once-weekly subcutaneous autoinjector for moderate to severe SLE based on phase 3 TULIP-SC trial results.
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The decision is made off findings from the 2 phase 3, randomized, double-blind, placebo-controlled POETYK PsA-1 and POETYK PsA-2 trials.

The FDA designates litifilimab as a breakthrough therapy for cutaneous lupus erythematosus, highlighting its potential to transform treatment options.