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. 2019 Apr 25;63(5):e02083-18. doi: 10.1128/AAC.02083-18

TABLE 4.

Investigator assessment of clinical response to omadacycline (safety population)

Parameterb No. (%) of patients in groupa:
1 (i.v. 200 mg →
p.o. 300 mg [n = 11])
2 (p.o. 300 mg
[n = 10])
3 (p.o. 450 mg
[n = 10])
End of treatment
    Clinical success 10 (90.9) 10 (100) 9 (90.0)
    Clinical failure 0 0 1 (10.0)
    Indeterminate 1 (9.1) 0 0
Posttreatment evaluation
    Clinical success 11 (100) 7 (70.0) 8 (80.0)
    Clinical failure 0 2 (20.0) 2 (20.0)
    Indeterminate 0 1 (10.0) 0
a

Omadacycline doses are given in parentheses after each group. i.v., intravenous; p.o., oral.

b

Clinical success indicates resolution of signs and symptoms and no use of additional systemic antimicrobial therapy for the urinary tract infection. Clinical failure indicates no apparent response to therapy, persistence of signs and symptoms of infection at the end-of-treatment visit, or the use of additional systemic antimicrobial therapy for the current infection. Indeterminate indicates that the visit was not completed.