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NCT07266324Possibly a fitNot yet recruiting

Study of BMB-101 for people with Prader-Willi syndrome

Prader-Willi Syndrome

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

This study tests an experimental drug called BMB-101 to see if it can help reduce the constant hunger (hyperphagia) that is common in Prader-Willi syndrome. The trial will check how safe and effective the drug is, and if it works, it may offer a new treatment option.

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

Phase
Phase 2
Enrollment
16 people
Ages
18 years to 65 years
Study type
Interventional

Who can take part

  • You must be between 18 and 65 years old.
  • You need a confirmed genetic diagnosis of Prader-Willi syndrome.
  • You must have moderate to severe hyperphagia, measured by a standard scale.
  • If you take growth hormone, you must have been on a stable dose for at least 90 days before the study starts.
  • You must not have certain heart, liver, or kidney problems.
  • You must be willing to use effective birth control during the study and for 90 days after the last dose.

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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