Wilson Disease is a rare genetic disorder caused by an inability to remove excess copper from the body. Too much copper can lead to issues like liver disease and neurological complications.
We appreciate your interest. See if you may qualify to participate, and let’s start a personalized conversation.
By submitting this form, you confirm that a diagnosis of Wilson Disease has been made by a medical professional.
*All fields are required.
At Ultragenyx, our goal is to bring novel therapies to patients with serious rare and ultra-rare genetic diseases. Since our founding in 2010, our team has had a proven track record of identifying, developing, and launching medicines for rare diseases. During this time, we’ve launched 3 FDA-approved treatments in 4 indications and developed a diverse portfolio of investigational therapies. We have deep expertise in multiple therapeutic areas, such as endocrine/bone diseases, metabolic diseases, and central nervous system (CNS)/muscle diseases. Most importantly, we put patients and their caregivers at the center of our work. All our efforts are rooted in our commitment to provide patients and their families with hope today.
One of our medical representatives will be reaching out to you shortly to continue the conversation. Please check your spam inbox if a confirmation email is not received within 5 business days.
Clinical trials help provide invaluable information to empower healthcare professionals to treat, diagnose, or discover new breakthroughs in treating disease. By choosing to participate in a clinical trial, people may help advance treatments, provide crucial insights, and ultimately improve the quality of life for others. A person might also benefit in learning more about their condition, gain access to specific care, or achieve faster access to treatment.