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Post-menopausal Vasomotor Symptoms clinical trials

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NCT ID: NCT02865538 Completed - Clinical trials for Post-menopausal Vasomotor Symptoms

Evaluation of the Pharmacokinetics and Safety of NT-814 in Post-Menopausal Women With Vasomotor Symptoms

Start date: August 2016
Phase: Phase 1/Phase 2
Study type: Interventional

This is a multi-center, double-blind, randomized, placebo-controlled multiple ascending dose study in post-menopausal women with vasomotor symptoms. Single ascending doses of NT-814 will be investigated in 4 cohorts. Each cohort will comprise of 20 subjects. Subjects will be dosed for 14 days.