Mirum Pharmaceuticals to Participate in Upcoming Investor Conferences
08 11월 2024 - 6:30AM
Business Wire
Mirum Pharmaceuticals, Inc. (Nasdaq: MIRM), a biopharmaceutical
company focused on the identification, acquisition, development and
commercialization of novel therapies for debilitating rare and
orphan diseases, today announced that it will participate in the
following upcoming investor conferences:
- Stifel 2024 Healthcare Conference on Tuesday, November 19th
- Company presentation - Tuesday, November 19th starting at 10:20
a.m. ET
- 7th Annual Evercore HealthCONx Conference on Tuesday, December
3rd
- Company presentation - Tuesday, December 3rd starting at 2:10
p.m. ET
- Citi’s 2024 Global Healthcare Conference on Wednesday, December
4th
Visit the Investors and Media section of Mirum’s corporate
website for webcast links and additional information.
About Mirum Pharmaceuticals, Inc.
Mirum Pharmaceuticals, Inc. is a biopharmaceutical company
dedicated to transforming the treatment of rare diseases affecting
children and adults. Mirum has three approved medications:
LIVMARLI® (maralixibat) oral solution, CHOLBAM® (cholic acid)
capsules, and CHENODAL® (chenodiol) tablets.
LIVMARLI, an IBAT inhibitor, is approved for the treatment of
two rare liver diseases affecting children and adults. It is
approved for the treatment of cholestatic pruritus in patients with
Alagille syndrome in the U.S. (three months and older), in Europe
(two months and older), and in other regions globally. It is also
approved in the U.S. in cholestatic pruritus in PFIC patients 12
months of age and older; in Europe, it is approved for patients
with PFIC three months of age and older. Mirum is also initiating
the Phase 3 EXPAND study, a label expansion opportunity for
LIVMARLI in additional settings of cholestatic pruritus. CHOLBAM is
FDA-approved for the treatment of bile acid synthesis disorders due
to single enzyme deficiencies and adjunctive treatment of
peroxisomal disorders in patients who show signs or symptoms or
liver disease. CHENODAL has received medical necessity recognition
by the FDA to treat patients with cerebrotendinous xanthomatosis
(CTX).
Mirum’s late-stage pipeline includes two investigational
treatments for debilitating liver diseases. Volixibat, an IBAT
inhibitor, is being evaluated in two potentially registrational
studies including the Phase 2 VISTAS study for primary sclerosing
cholangitis (PSC) and Phase 2b VANTAGE study for primary biliary
cholangitis. Volixibat has been granted Breakthrough Therapy
Designation for the treatment of cholestatic pruritus in patients
with PBC. Lastly, chenodiol, has been evaluated in a Phase 3
clinical study, RESTORE, to treat patients with CTX, with positive
topline results reported in 2023. Mirum has submitted a new drug
application with the FDA for the approval of chenodiol to treat CTX
in the U.S.
To learn more about Mirum, visit mirumpharma.com and follow
Mirum on Facebook, LinkedIn, Instagram and Twitter (X).
View source
version on businesswire.com: https://www.businesswire.com/news/home/20241107101895/en/
Investors: Andrew McKibben ir@mirumpharma.com
Media: Erin Murphy media@mirumpharma.com
Mirum Pharmaceuticals (NASDAQ:MIRM)
과거 데이터 주식 차트
부터 10월(10) 2024 으로 11월(11) 2024
Mirum Pharmaceuticals (NASDAQ:MIRM)
과거 데이터 주식 차트
부터 11월(11) 2023 으로 11월(11) 2024