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Approved Uses and Current Clinical Evidence in the UK Neither cagrilintide nor retatrutide is licensed by the MHRA or EMA
The rates of clinical response after escalating to an HD IFX regimen [84.9% and 62.3% at the early and late time periods, respectively] closely parallel the response rates of 6696% seen in other studies examining standard escalation from 5mg/kg every 8 weeks to 5mg/kg every 4 weeks or to 10mg/kg every 8 weeks

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Switching biologic agent in patients with psoriasis: A systematic review and meta-analysis

However, underlaying mechanisms remain understudied

10.1017/s095026881000052x 21 EndoH.HigurashiT.HosonoK.SakaiE.SekinoY.IidaH.et al (2011)
