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Recruiting

NCT Number: NCT06545877

REKOVELLE PEN for S.C. Injection General Drug Use Survey (Controlled Ovarian Stimulation in Assisted Reproductive Technologies)

This survey targets controlled ovarian stimulation with this drug for the development of multiple oocytes in women undergoing assisted reproduction (ART) such as in vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI).

Recruiting

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Key information

Sex eligibility

Female

Study type

Observational

Primary location

Ferring Investigational Site

Omitama, Ibaraki, Japan

Location status: Recruiting

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants who received the REKOVELLE in controlled ovarian stimulation in assisted reproductive technologies and have consented to participate in the survey.

Exclusion criteria

  • No exclusion criteria because data are collected under conditions of use in daily practice.

Treatment and study plan

Primary outcomes

  1. Adverse Events

    Time frame: From initiation of the administration, in case of embryo transfer is not performed, until 1 week after oocyte collection, and in case embryo transfer is performed, 6 weeks after embryo transfer

    Frequency of Adverse Events

Study contacts

Contact information is provided by the study sponsor or research team.

Global Clinical Compliance

CONTACT

[email protected]

+1 833-548-1402 (US/Canada)

Global Clinical Compliance

CONTACT

[email protected]

+1 862-286-5200 (outside US)

Sponsors and collaborators

Lead sponsor

Ferring Pharmaceuticals

Industry

Registry information

Official study title

REKOVELLE® PEN S.C. Injection 12μg/36μg/72μg for Controlled Ovarian Stimulation in Assisted Reproductive Technologies - General Drug Use-results Survey

Important dates

Study start
2022
Primary completion
2026
Study completion
2029
First posted
Aug 9, 2024
Registry last updated
Aug 20, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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