Clin2
NCT05908682Possibly a fitRecruiting

Study of ibrexafungerp safety during pregnancy

Vulvovaginal CandidiasisCandida InfectionVaginal Candidiasis

Part of Infections, Mouth & dental, Women’s health & pregnancy clinical trials.

This study looks at what happens when ibrexafungerp is taken during pregnancy, including outcomes for the baby. You may join if you were exposed to this medicine during pregnancy (or very close to conception) and you agree to share information and complete study follow-up.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
100 people
Ages
birth and older
Study type
Observational

Who can take part

  • You were exposed to ibrexafungerp during pregnancy
  • OR conception likely happened within 4 days after your last ibrexafungerp dose
  • You can provide consent (you or your legal representative) to join the study
  • You can do pregnancy testing if needed (a positive urine test confirms pregnancy for this study)
  • You can give accurate medical history and allow medical record sharing

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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