Clin2
NCT06225882Likely a fitRecruiting

Follow-up study for patients with primary hyperoxaluria type 1 on Lumasiran

Patients With PH1 Treated With Lumasiran in France

Part of Genetic & congenital, Kidney & urinary clinical trials.

This study follows patients with primary hyperoxaluria type 1 who are being treated with Lumasiran. It aims to understand how well the treatment works over time.

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

Phase
N/A
Enrollment
100 people
Ages
birth to 99 years
Study type
Observational

Who can take part

  • You have primary hyperoxaluria type 1 (a rare disease that causes too much oxalate in your body).
  • You have been treated with Lumasiran (a medication that lowers oxalate levels).
  • You started treatment as part of a temporary authorization program or after it was approved for use.

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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