77 Remission (HAMD‐17 total score ≤ 7) was observed in 7 of 10 patients in the brexanolone group compared to 1 of 11 patients in the placebo group at 60 hours ( P = .0364), whereas response rates (50% or greater reduction from baseline in total HAMD‐17 score) did not reach statistical significance between groups (7 in 10 patients in the brexanolone group compared to 4 of 11 patients in the placebo group; P = .1450). 77 There were no serious adverse events (AEs) or discontinuations in either group, and the most frequent AEs in the brexanolone group were dizziness (2 patients in the brexan
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Development of neuroactive steroids for the treatment of postpartum depression.
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0.1450