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Menopur And Rekovelle Combination Study — MARCS  

Fertility Disorders Clinical Trial

Official title:
An Exploratory Study to Evaluate a Mixed Protocol of Menopur (Highly Purified Human Menopausal Gonadotropin) and REKOVELLE (Follitropin Delta) for Controlled Ovarian Stimulation in IVF (in Vitro Fertilization)

Clinical Trial Summary

This study proposes to evaluate the effect of adding HP-hMG (Menopur) to follitropin delta in a "mixed protocol" regimen, using an individualized, fixed dose of follitropin delta based on the established algorithm, combined with a variable, adjustable dose of Menopur based on body weight and ovarian reserve.

Clinical Trial Description

The initial dose of follitropin delta will be determined at enrolment by the analysis of serum AMH on days 2 to 5 of the menstrual cycle preceding the IVF treatment cycle and body weight in Kg The initial dose of HP-hMG to be added on top of follitropin delta will be determined at enrolment by the total follitropin delta dose and body weight in Kg ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03483545
Study type Interventional
Source OVO R & D
Contact
Status Completed
Phase N/A
Start date July 17, 2018
Completion date July 31, 2019
View Details
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