RBC Capital Markets Global Healthcare Conference 2026
Logotype for Mirum Pharmaceuticals Inc

Mirum Pharmaceuticals (MIRM) RBC Capital Markets Global Healthcare Conference 2026 summary

Event summary combining transcript, slides, and related documents.

Logotype for Mirum Pharmaceuticals Inc

RBC Capital Markets Global Healthcare Conference 2026 summary

20 May, 2026

Strategic overview and recent developments

  • Operating as a global rare disease company with 430 employees and three approved medicines, including LIVMARLI, which has expanded from pediatric to adult populations.

  • Two major clinical data readouts this quarter: positive pivotal data from the VISTAS study in primary sclerosing cholangitis and a phase II-B readout in hepatitis delta following the Bluejay Therapeutics acquisition.

  • Announced a new business development (BD) transaction for an ultra-rare disease medicine, expanding the portfolio.

  • BD strategy focuses on high unmet medical needs, conviction in biology, and disciplined deal selection, with recent deals spanning commercial to phase II-ready assets.

  • Recent capital raise refinanced convertible notes at a 0% coupon, improving financial flexibility without altering BD approach.

Commercial performance and market dynamics

  • LIVMARLI achieved $114 million in Q1 2026 net sales, up 55% year-over-year, with full-year guidance raised to $660–$680 million.

  • Growth driven by strong demand in PFIC, especially later-onset cases, and better-than-expected international sales.

  • Alagille syndrome market penetration is about 50%, with continued steady patient additions; PFIC market is split 50/50 with competitor BYLVAY.

  • Significant growth potential remains, particularly as adult providers increase genetic testing for PFIC.

  • The EXPAND phase III study could further boost LIVMARLI, with potential for over $1 billion in peak sales across indications.

Pipeline progress and clinical milestones

  • VISTAS phase IIb study in PSC met its primary endpoint, with full data to be presented at EASL; opportunity for volixibat remains over $1 billion.

  • Study design elements, such as placebo run-in periods and patient training, have effectively reduced noise in pruritus trials.

  • Interim results in the VANTAGE study for PBC are promising, with expectations to outperform competitors on pruritus improvement.

  • Pricing strategy for volixibat will be determined after further data and competitor pricing are available, aiming to maximize access and value.

  • Combination therapy with PPAR agonists is possible in PBC, with IBATs targeting pruritus where other therapies may not suffice.

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