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Study of Nolasiban to Increase Pregnancy Rates in Women Undergoing IVF — IMPLANT4  

Infertility Clinical Trial

Official title:
A Phase 3, Double-blind, Randomized, Placebo-controlled Study to Assess the Safety and Efficacy of a Single Oral Administration of Nolasiban to Increase On-going Pregnancy Rate Following Fresh Single Blastocyst Transfer Resulting From IVF

Clinical Trial Summary

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

Clinical Trial Description

The study is a prospective, randomised, parallel group, double-blind, placebo-controlled, Phase 3 study to confirm the efficacy and the safety of nolasiban versus placebo to increase pregnancy and live birth rates in 820 women undergoing fresh single blastocyst transfer following in vitro fertilisation (IVF) or intra-cytoplasmic sperm injection (ICSI). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03758885
Study type Interventional
Source ObsEva SA
Contact
Status Completed
Phase Phase 3
Start date January 10, 2019
Completion date November 11, 2020
View Details
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