drugset / Trial / NCT03081208

Phase 3 Placebo Controlled Study of Nolasiban to Improve Pregnancy Rates in Women Undergoing IVF/ICSI

NCT03081208 ↗

Phase 3 Completed 810 enrolled ObsEva SA
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to confirm the efficacy of a single oral 900mg dose of nolasiban to increase the ongoing clinical pregnancy rate at 10 weeks post embryo transfer (ET) day.

Timeline

Start
2017-03-06
Primary completion
2018-03-21
Completion
2019-02-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Nolasiban Small molecule 900 mg Oral

Indications