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NCT07482787Possibly a fitRecruiting

Study of SD-101 for epidermolysis bullosa in children

Epidermolysis Bullosa (EB)

Part of Genetic & congenital, Skin clinical trials.

This trial tests a new medicine called SD-101 for children with epidermolysis bullosa (EB), a condition that causes fragile skin and blistering. It aims to see if SD-101 can help heal wounds and improve quality of life.

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

Phase
Phase 3
Enrollment
80 people
Ages
4 weeks to 12 years
Study type
Interventional

Who can take part

  • Your child is between 28 days and 12 years old.
  • Your child has been diagnosed with simplex, recessive dystrophic, or intermediate junctional EB.
  • Your child has at least one wound that is 10 to 50 square centimeters (about the size of a credit card to a small hand) and has been present for at least 21 days.
  • The total skin affected by wounds is at least 5% of their body surface area.
  • Your child has not used certain treatments (like steroids, antibiotics, or other investigational drugs) within the past month.
  • Your child does not have a current or past cancer.

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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