While the primary endpoint (adapted ACR 30) was achieved in all cases, the high-dose group showed a trend toward efficacy in several secondary endpoints compared with the other groups.
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A Phase-II Investigator-Initiated Randomized, Double-Blind, Parallel-Group Clinical Trial of 5-Aminolevulinic Acid Hydrochloride/Sodium Ferrous Citrate (5-ALA-HCl/SFC) for Patients With Adult-Onset Still's Disease (AOSD) Refractory to Corticosteroids.
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