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Efficacy and Safety of BG2109 During Controlled Ovarian Hyperstimulation in Female Subjects Undergoing ART Procedures

Assisted Reproductive Technology Clinical Trial

Official title:
A Randomized, Double-blind, Open for Active Comparator, Parallel, Multi-center Phase II Study to Explore the Efficacy, Safety and Tolerability of BG2109 Compared With Cetrorelix During COH in Female Subjects Undergoing ART Procedures

Clinical Trial Summary

To explore the optimal effective daily dose of BG2109 to suppress premature luteinizing hormone (LH) surge during COH in female subjects undergoing ART procedures.

Clinical Trial Description

This study is a randomized, double-blind, open for active comparator, parallel, multi-center phase II dose-finding clinical study to explore the efficacy, safety and tolerability of different doses of BG2109 compared with Cetrorelix during Controlled Ovarian Hyperstimulation (COH) in Chinese female subjects undergoing Assisted Reproductive Technology (ART) procedures. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05738382
Study type Interventional
Source Bio Genuine (Shanghai) Biotech Co., Ltd.
Contact Jing Zhao
Phone 021-58590032
Email Jing.zhao@Biogenuine.con
Status Not yet recruiting
Phase Phase 2
Start date August 2023
Completion date December 2024
View Details
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