Clin2
NCT06126380Possibly a fitEnrolling by invitation

Long-term safety of tegoprubart in kidney transplant patients

Kidney Transplant Rejection

Treatments studied

Part of Kidney & urinary, Women’s health & pregnancy clinical trials.

This is a long-term follow-up study for people who have already completed a study of the drug tegoprubart after a kidney transplant. It checks how safe and effective the drug is over a longer period.

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

Phase
Phase 2
Enrollment
132 people
Ages
18 years to 100 years
Study type
Interventional

Who can take part

  • You must have completed an earlier (parent) study that offered you the chance to join this long-term follow-up.
  • You must be able to understand the study information and agree to the consent form.
  • You must agree not to take part in any other research study while on this treatment.
  • If you could become pregnant, you need a negative pregnancy test before starting and must use effective birth control during and for 90 days after the last dose.
  • If you are a man with a partner who could become pregnant, you must use effective birth control and not donate sperm for 90 days after the last dose.
  • You cannot be pregnant or breastfeeding.

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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