drugset / Trial / NCT00335569

Clinical Tolerance and Equivalence of hCG-IBSA vs Recombinant Human Chorionic Gonadotrophin in Women Undergoing In Vitro Fertilisation

NCT00335569 ↗

Phase 3 Completed 144 enrolled IBSA Institut Biochimique SA
RandomizedParallel-groupSingle-blindTreatment

Summary

The purpose of the study is to evaluate the clinical equivalence and the general tolerability of two different subcutaneous hCG preparations (hCG-IBSA, IBSA vs Ovitrelle, Serono) when administered to patients undergoing IVF.

Timeline

Start
2005-08
Primary completion
—
Completion
2008-12

Outcome

Met primary endpoint

paper The number of retrieved oocytes was not inferior when HP-hCG was used as compared to r-hCG: PMID 23116325 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject hCG-IBSA Unknown — Subcutaneous

Indications