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Description
The approval was backed by the Phase II open-label AGAVE-201 trial, where treatment with a 0.3-mg/kg dose of Niktimvo elicited an overall response rate of 75%, with a median time to response of 1.5 months
doi: 10.3390/ijms22115996 32 DomonHTeraoY
DOI: 10.46497/ArchRheumatol.2022.9109
The therapy causes much higher levels of high-sensitivity C-reactive protein (hs-CRP) in about 70% of patients
doi: 10.1038/s41593-023-01315-6
