Clin2
NCT07820085Possibly a fitRecruiting

Oral treatment for light sensitivity in EPP and XLP

Erythropoietic Protoporphyria (EPP)X-Linked Protoporphyria (XLP)EPP2

Part of Digestive system, Genetic & congenital, Hormones & metabolism, Skin clinical trials.

This study tests an oral medication, PORT-77, to reduce pain and sensitivity to sunlight in people with EPP or XLP. It may help those who experience symptoms shortly after sun exposure.

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

Phase
Phase 2/Phase 3
Enrollment
225 people
Ages
12 years and older
Study type
Interventional

Who can take part

  • Be at least 12 years old
  • Have a confirmed diagnosis of EPP or XLP
  • Experience symptoms of sun sensitivity within about 45 minutes of sun exposure
  • Be willing to fill out a daily symptom diary and follow study procedures
  • Meet weight or body mass index (BMI) criteria (weight ≥32 kg for ages 12-17, BMI ≥18.5 for adults)
  • Not be taking certain light-sensitivity medications or supplements (e.g., afamelanotide, beta carotene) within 90 days before the study starts

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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