Mirum Pharmaceuticals (MIRM) Q3 2026 earnings summary
Event summary combining transcript, slides, and related documents.
Q3 2026 earnings summary
3 Nov, 2026Executive summary
Q3 net product sales were $185.7M; FY 2026 guidance rose to $715M-$720M as commercial growth and pipeline progress continued.
Four medicines are approved; five potential regulatory actions and portfolio peak revenue potential above $4B were cited.
Financial highlights
Q3 product sales were $185.7M vs. $133.0M year over year; nine-month sales were $521.8M vs. $372.4M.
Q3 operating loss was $59.7M vs. operating income of $2.6M; net loss was $40.8M vs. net income of $2.9M.
Nine-month net loss was $898.1M, including $756.2M of acquired IPR&D expense; nine-month operating loss was $891.7M.
Q3 operating expenses were $245.5M; cash-adjusted R&D was $93.6M, SG&A $70.4M and cost of sales $27.9M.
Q3 basic/diluted loss per share was $0.62/$0.87; nine-month basic and diluted loss per share was $14.35.
Outlook and guidance
FY 2026 net product sales guidance increased to $715M-$720M, reflecting growth across LIVMARLI and bile acid medicines; adult PFIC was the largest growth driver.
H1 2027 submissions planned for volixibat PSC NDA, LIVMARLI EXPAND sNDA, ATEBRIOZ pediatric sNDA and brelovitug BLA, subject to supportive AZURE-4 results.
Brelovitug AZURE-4 results expected Q4 2026; volixibat VANTAGE PBC topline data expected Q1 2027; MRM-3379 BLOOM topline data expected in 2027.
Management expects quarterly total revenue growth of $10M-$15M through 2027 and cash-flow positivity next year; net losses are expected to continue as pipeline investment proceeds.
If approved, brelovitug U.S. launch is anticipated in Q4 2027.
Latest events from Mirum Pharmaceuticals
- Four approved medicines, with 2027 catalysts in HDV, PSC and PBC.MIRM
Stifel 2026 Healthcare Conference 2026 - Five 2027 filings, expanding rare-disease launches and a return to positive cash flow.MIRM
8th Annual Wolfe Research Healthcare Conference - Four approved medicines anchor growth as late-stage rare-disease programs advance.MIRM
Corporate presentation - Brelovitug met its Week 24 primary endpoint at both doses in chronic hepatitis D.MIRM
Conference presentation - A growing rare-disease portfolio pairs $715M–$720M 2026 sales guidance with key 2027 milestones.MIRM
Corporate presentation - 2025 sales reached $521.3M as positive late-stage results set up 2027 filings.MIRM
Corporate presentation - EXPAND met its primary endpoint, supporting a planned U.S. filing in H1 2027.MIRM
Study result - Rare disease portfolio delivers strong growth, late-stage pipeline, and robust clinical momentum.MIRM
Corporate presentation - Brelovitug met key efficacy and safety endpoints in chronic HDV, supporting 2027 approval plans.MIRM
Study result