Staying in
the know

We are committed to developing safe and effective therapies to help transform realities for those living with rare liver disease. But that also means helping you stay current and up to date on what is going on today. Learn more about resources that are available to provide support to you and your family.

to genetic

Mirum is working alongside Travere Therapeutics to provide support to
ensure qualified patients have access to the Emory Genetics Lab genetic
cholestasis panel at no charge. This panel may assist in diagnosing a
cholestatic liver disease.

Support for living with a rare disease

Find support for people and families living with rare disease:

Information about progressive familial
intrahepatic cholestasis (PFIC)
Information about intrahepatic cholestasis of pregnancy (ICP)
Information about primary sclerosing cholangitis (PSC)

LIVMARLITM (maralixibat)
oral solution

Mirum’s Expanded Access Program (EAP) offers access to
LIVMARLI (maralixibat) for the treatment of cholestatic pruritus
in eligible patients in Australia, Canada, the UK and several
countries in Europe.

Mirum Access Plus (MAP)

Designed to help patients and families start and stay on
LIVMARLI (maralixibat), this program connects patients and
families with MAP experts who can help educate on the
journey, from treatment access to financial support.