To Investigate REKOVELLE in Chinese Women Undergoing Assisted Reproductive Technologies: Effectiveness, Safety, and Patterns of Use in Real-world Practice

Recruiting Observational Study
Infertility
No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
20 and older
Sex
Female
Study type
Observational
Participants needed
2,500 (estimated)
Sponsor
Ferring Pharmaceuticals · Industry
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About This Trial
This is a multi-centre prospective non-interventional trial to assess the pattern of use of REKOVELLE® in Women Undergoing In Vitro Fertilisation (IVF) or Intracytoplasmic Sperm Injection (ICSI) Procedures in Routine Clinical Practice. There will be approximately 2500 patients initiated with REKOVELLE® treatment and enrolled in 30-50 sites in China. The total duration of the study will be approxi…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Women who meet all the following criteria are eligible for participation: * At least 20 years of age (including the 20th birthday) when signing informed consent * Prescribed REKOVELLE for the first time in controlled ovarian stimulation for in vitro fertilisation (IVF) or…
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