Clin2
NCT07150013Possibly a fitRecruiting

Vorinostat for Rett syndrome safety study

Rett Syndrome

Treatments studied

Part of Brain & nervous system, Genetic & congenital clinical trials.

This trial tests whether vorinostat is safe and helpful for girls and young women with Rett syndrome. Participants must have a confirmed MeCP2 mutation and be in a stable phase of the condition.

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

Phase
Phase 1
Enrollment
15 people
Ages
6 years to 21 years
Study type
Interventional

Who can take part

  • Female aged 6 to 21 years
  • Diagnosed with typical Rett syndrome with a confirmed MeCP2 mutation
  • No worsening of walking, hand use, talking, or communication in the past 4 months
  • Stable medications (including seizure meds) for at least 4 weeks before starting; if taking trofinetide, stable for 6 months
  • Able to swallow capsules or take them through a feeding tube
  • Willing to wear a small activity monitor on wrist or ankle

View the official record on ClinicalTrials.gov

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

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