Apply to trial NCT07587021

A few quick questions so the study team can decide if you might be a fit.

RecruitingPhase 2Genetic intervention

Study of YOLT-203 in Children and Adults With Primary Hyperoxaluria Type 1 (PH1)

This study will be conducted to evaluate the efficacy and safety of YOLT-203 in children and adults with Primary Hyperoxaluria Type 1. After the initial randomized, 6-month double-blind, placebo-controlled period, participants who were initially assigned to placebo will receive a single-dose of YOLT-203 treatment whereas participants in the YOLT-203 group will receive a single-dose of placebo infusion. For patients interested in additional information on how to participate, please follow this link: https://mytomorro.ws/ph1trial.

How this works

Answer a few questions
About 5 to 10 minutes. Skip-friendly where possible.
We connect you with the study team
When a site picks up your application, we introduce you to their team directly — with you on the thread.
The team reaches out to schedule screening
Usually within a few business days, via the contact you give.

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Study of YOLT-203 in Children and Adults With Primary Hyperoxaluria Type 1 (PH1)

How this works

Answer a few questions

We connect you with the study team

The team reaches out to schedule screening