Corifollitropin alfa N02 versus recombinant FSH for ovarian stimulation: a phase 3 trial and safety study in Chinese women.

Reprod Biomed OnlineJun 11, 2026 (epub)
Clinical ResearchObstetrics & Gynecology

Tingting Li, Xiujuan Chen, Yingpu Sun et al.

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In 30 seconds

This phase 3 randomized controlled trial evaluated the efficacy and safety of corifollitropin alfa N02 compared to daily recombinant FSH (rFSH) for ovarian stimulation in 474 Chinese women aged 20-39 with normal ovarian reserve. The corifollitropin alfa N02 group retrieved a mean of 12.1 oocytes, demonstrating non-inferiority to the 10.9 oocytes retrieved in the rFSH group.

Key findings

  • Mean oocytes retrieved: 12.1 for corifollitropin alfa N02 vs 10.9 for daily rFSH.
  • Clinical pregnancy rate: 46.3% in corifollitropin alfa N02 group vs 51.1% in rFSH group.
  • Ovarian hyperstimulation syndrome occurred in 3.8% of corifollitropin alfa N02 group vs 2.5% in rFSH group.
  • Birth defect rate: 7.6% for corifollitropin alfa N02 vs 12.0% for daily rFSH.

Why it matters

The findings suggest that corifollitropin alfa N02 provides a viable alternative to daily rFSH for ovarian stimulation, potentially simplifying treatment protocols while maintaining similar efficacy and safety profiles.

Source

Published in Reprod Biomed Online. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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