Clinical Trials Directory

Trials / Completed

CompletedNCT02458768

Multicenter, Randomized, Open Label, Parallel Study to Evaluate the Efficacy & Safety of IVF-M HP Inj. vs. Menopur® Inj.

A Multicenter, Randomized, Open Label, Parallel Study to Evaluate the Efficacy & Safety of s.c. Administration of IVF-M HP Inj. Versus Menopur® Inj. in Infertility Women Undergoing Controlled Ovarian Hyperstimulation for Assisted Reproductive Technologies (ART) Such as in Vitro Fertilization-embryo Transfer (IVF-ET)

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
112 (actual)
Sponsor
LG Life Sciences · Industry
Sex
Female
Age
20 Years – 39 Years
Healthy volunteers
Not accepted

Summary

The objective of this study was to demonstrate the non-inferiority of IVFM HP Inj. by evaluating its efficacy versus Menopur® Inj. in infertility women undergoing the in vitro fertilization and embryo transfer (IVF-ET) among the assisted reproductive technologies.

Conditions

Interventions

TypeNameDescription
DRUGIVF-M HP Inj.
DRUGMenopur® Inj.

Timeline

Start date
2013-07-01
Primary completion
2014-11-01
First posted
2015-06-01
Last updated
2016-02-03
Results posted
2016-02-03

Source: ClinicalTrials.gov record NCT02458768. Inclusion in this directory is not an endorsement.

Multicenter, Randomized, Open Label, Parallel Study to Evaluate the Efficacy & Safety of IVF-M HP Inj. vs. Menopur® Inj. (NCT02458768) · Clinical Trials Directory