Apply to trial NCT05502133

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

Recruiting

Identification of Acute Intermittent Porphyria Modifying Genes

This study proposes to identify the predisposing/protective modifying genes that underlie the acute attacks in symptomatic patients with Acute Intermittent Porphyria (AIP), an autosomal dominant inborn error of heme biosynthesis.

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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Identification of Acute Intermittent Porphyria Modifying Genes

How this works

Answer a few questions

We connect you with the study team

The team reaches out to schedule screening