Corporate presentation
Logotype for Mirum Pharmaceuticals Inc

Mirum Pharmaceuticals (MIRM) Corporate presentation summary

Event summary combining transcript, slides, and related documents.

Logotype for Mirum Pharmaceuticals Inc

Corporate presentation summary

28 Sep, 2026

Strategic overview and financial performance

  • Focused on delivering high-impact medicines for rare liver and genetic diseases, with a portfolio targeting multi-billion dollar revenue potential and a 2026 net product sales guidance of $680–700M.

  • Five approved indications and four in late-stage development, with five FDA Breakthrough Therapy Designations and over $4B estimated peak revenue potential.

  • Commercial portfolio includes Livmarli, Ctexli, Cholbam, and ATEBRIOZ, with significant year-over-year sales growth and global commercial reach.

  • Cash flow positive expected in 2027, supported by a $561M cash balance as of June 2026.

Pipeline and clinical development

  • Livmarli is approved for Alagille syndrome (ALGS) and progressive familial intrahepatic cholestasis (PFIC), with label expansion opportunities in ultra-rare cholestatic pruritus.

  • Volixibat demonstrated positive Phase 2b results in primary sclerosing cholangitis (PSC) and primary biliary cholangitis (PBC), with NDA submissions targeted for 2027.

  • Brelovitug showed efficacy and favorable safety in chronic hepatitis delta virus (HDV), meeting primary endpoints in Phase 3 and supporting FDA/EMA submissions.

  • ATEBRIOZ (zilurgisertib) received FDA approval for fibrodysplasia ossificans progressiva (FOP), with ongoing studies in younger patients.

  • MRM-3379, a PDE4D inhibitor for Fragile X syndrome (FXS), is in Phase 2 with topline data expected in 2027.

Market opportunity and patient impact

  • Addressable markets include rare liver diseases (ALGS, PFIC, PSC, PBC, HDV) and rare genetic diseases (CTX, BASD, FOP, FXS), with significant unmet needs and high symptom burden.

  • Livmarli demonstrated substantial improvements in pruritus, serum bile acids, and transplant-free survival in ALGS and PFIC patients.

  • Volixibat and brelovitug address pruritus and disease progression in PSC, PBC, and HDV, with strong clinical data supporting efficacy and safety.

  • Bile acid replacement therapies (Cholbam, Ctexli) address multiple high-need genetic settings, with growing commercial synergies.

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