Clin2
NCT07262268Worth exploringEnrolling by invitation

Testing BHV-7000 for inherited erythromelalgia pain

Familial Erythromelalgia

Treatments studied

Part of Brain & nervous system, Heart & circulation, Pain clinical trials.

This clinical trial tests an investigational medication (BHV-7000) for people with inherited erythromelalgia caused by a specific NaV1.7 gene mutation. The study aims to see if the drug can safely reduce the chronic burning pain that is typical of this condition.

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

Phase
Phase 1
Enrollment
5 people
Ages
18 years to 75 years
Study type
Interventional

Who can take part

  • You are between 18 and 75 years old.
  • You have a confirmed inherited form of erythromelalgia (a rare condition causing severe burning pain in hands/feet) caused by a specific NaV1.7 gene change.
  • You do not have a different genetic change (Kv7.2/7.3) that affects nerve channels.
  • Your pain medicines have been stable for the last 30 days and you can keep them the same during the study.
  • You can and will stick to the study schedule, including filling out daily pain diaries.

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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