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Potential limitations of both studies include the use of a single dose rather than multiple doses of cagrilintide and the use of doses (0.6 mg in the renal impairment study and 0.9 mg in the hepatic impairment study) lower than the 2.4 mg dose being evaluated in clinical development
However, all adverse events should be closely monitored and clearly reported in the results section of the RCT publication, typically using a detailed table to break down the adverse events experienced and the proportion of the participants who experienced them in each treatment group [36]
Thanks Kenny, cant wait to come back!!Posted onGage FloryTrustindex verifies that the original source of the review is Google.Extremely professional, clean, and well run
Everything else is just plugging in numbers
2002;56(11):113742 Hojs R, Bevc S, Antolinc B, Gorenjak M, Puklavec L
