The remaining health‐related QoL parameters in the 50 and 25 μg desmopressin ODT groups showed an improvement compared with placebo, although the differences did not reach statistical significance (Table 4 ).
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Efficacy and safety of 25 and 50 μg desmopressin orally disintegrating tablets in Japanese patients with nocturia due to nocturnal polyuria: Results from two phase 3 studies of a multicenter randomized double-blind placebo-controlled parallel-group development program.
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