#TeamMirum will be hitting the road to present at three upcoming congresses in May. We’ll be at #DDW2025, #EASLCongress and #ESPGHAN25. Will you be there? Let us know in the comments. https://bit.ly/3GrQ54d
Mirum Pharmaceuticals, Inc.
Pharmaceutical Manufacturing
Foster City, CA 37,830 followers
Creating transformative medicine for people with rare disease.
About us
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 CTEXLI™ (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 of liver disease. CTEXLI is FDA-approved for the treatment of cerebrotendinous xanthomatosis (CTX) in adults. Mirum's late-stage pipeline includes two investigational treatments for several rare 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. Mirum is also planning for a Phase 2 study evaluating MRM-3379, a PDE4D inhibitor for the treatment of Fragile X syndrome, a rare genetic neurocognitive disorder.
- Website
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https://mirumpharma.com/
External link for Mirum Pharmaceuticals, Inc.
- Industry
- Pharmaceutical Manufacturing
- Company size
- 201-500 employees
- Headquarters
- Foster City, CA
- Type
- Public Company
- Founded
- 2018
Locations
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Primary
Get directions
989 E Hillsdale Blvd.
Suite 300
Foster City, CA 94404, US
Employees at Mirum Pharmaceuticals, Inc.
Updates
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We are proud to be a Presenting Sponsor at the inaugural Cholestatic Liver Disease Summit hosted by the Alagille Syndrome Alliance, BAREinc.org, and PFIC Network. Will you be there? Let us know in the comments! 👇
THANK YOU to Mirum Pharmaceuticals, Inc. for being a 2025 Cholestatic Liver Disease Summit Presenting Sponsor! Mirum has been in the field of pediatric cholestatic liver disease since the company began. We are thrilled to have their Presenting Sponsorship and appreciate their impactful and continuing work! Are you registered to come to the Summit? If not, now is the time! Register at liverdiseasesummit.org, our event website, and check out the event details while you're there! You do not want to miss it! 2025 Cholestatic Liver Disease Summit presented by Mirum Pharmaceuticals - Planned in partnership with Alagille Syndrome Alliance, BAREinc.org, PFIC Network, and Children's Hospital Colorado. #ALGS #biliaryatresia #pfic #liverdisease #raredisease
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#ICYMI: Philipp Anstaett-Pfeifer took the stage at Reuters Events Pharma #REpharma conference sharing with attendees a playbook focused on rapid global expansion in rare disease. Were you in the room? We’d love to hear your top takeaways – drop them in the comments below! 👇
Philipp Anstaett-Pfeifer Mirum Pharmaceuticals, Inc. kicked things off with an engaging case study into accelerating rare disease breakthrough, providing a playbook for rapid global expansion - key takeaways? - Agile Mindset for Rapid Change - Adaptive Cross-Functional Readiness - Data-Driven Opportunity Prioritization - Collaborative Change Management - Rapid Recalibration to Changes #REpharma
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This week, Mirum’s Philipp Anstaett-Pfeifer will take the stage during Reuters Events Pharma 2025 in Barcelona, Spain. Philipp’s session, “Accelerate a Rare Disease Breakthrough: A Playbook for Rapid Global Expansion,” will dive into the challenges of rapid expansion as well as key pillars for success. Have you registered? For details about the conference and to register, visit https://bit.ly/3TAqjz1 #REPharma #RareDisease #GlobalExpansion #Pharma2025
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Our partner, Takeda, announced that LIVMARLI®(maralixibat) oral solution is now approved by the Japanese Ministry of Health, Labour, and Welfare in two pediatric cholestatic liver diseases. With more than 30 countries globally, we are thrilled to see LIVMARLI available to patients in need and excited for its potential with the new approval in Japan! Congratulations to the Takeda team! Read the news release: https://bit.ly/3FFPiw2 or follow Takeda for more information. #Approved #RareDisease
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Team Mirum is on the ground at #ACMG2025 and excited for a fantastic meeting. Stop by and visit us at booth 511 now through Saturday! Hope to see you there!
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We are proud to share that MM+M has recognized our very own Erin Osborne Murphy as a Woman of Distinction, Class of 2025! Join us in congratulating Erin and the other honorees on this wonderful award. 🎉🌟 #MMMWomenofDistinction
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Are you registered for the Rare Disease Summit? Join us in Philadelphia tomorrow for a special presentation with Chris Peetz, who will discuss the challenges and rewards of building a company focused on delivering treatments for some of the rarest diseases. Hope to see you there! For more information, visit https://lnkd.in/ghFFGVqR.
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Happy International Women’s Day (IWD)! Today offers an opportunity to reflect, acknowledge, and celebrate the incredible contributions women have made in our industry and beyond. We’re proud that so many remarkable women have chosen to work at Mirum where they are making a significant impact on the global rare disease community every day. #InternationalWomensDay #IWD2025
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Our hearts are heavy with the recent loss of Cathy Mumford, a truly extraordinary, passionate patient advocate for people living with Primary Biliary Cholangitis (PBC). Cathy was a fierce champion and dedicated leader who made a significant impact on the PBC community, including the patient community, families, researchers and industry. Her legacy will live on as one determined to make the future of PBC brighter for patients and their families. We share our deepest condolences with Cathy’s family, friends, and the PBCers organization. 🤍
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