Mirum Pharmaceuticals (MIRM) Stifel 2026 Healthcare Conference 2026 summary
Event summary combining transcript, slides, and related documents.
Stifel 2026 Healthcare Conference 2026 summary
11 Nov, 2026Financial outlook
2026 revenue guidance is $715M-$720M, with growth expected across all four approved medicines and significant 2027 contributions from recently approved ATEBRIOZ in FOP.
Cash-flow-positive guidance remains for 2027; cash flow was positive in 2025 and H1 2026, while H2 2026 includes elevated R&D and CMC investment for brelovitug and volixibat.
Volixibat in PSC and PBC
PSC filing is planned for H1 2027 after further FDA engagement; the FDA recommended Phase III at the July pre-NDA meeting but said filing could proceed at discretion, and plans remain on track.
A pre-planned PSC analysis found no IBD exacerbation signal, reassuring for the ~70% of PSC patients with IBD.
Estimated PSC population is ~50,000 in the U.S., with ~60% having significant itch warranting treatment; a similar number is estimated outside the U.S.
PBC data are expected in Q1 2027; 2024 interim results showed >2-point pruritus improvement plus sleep and fatigue improvements, supporting breakthrough designation and increased FDA dialogue.
PBC population is estimated at 80,000-100,000; ~1/3 are controlled on UDCA but still have itch, while volixibat may also address patients with inadequate control on PPARs.
Brelovitug and HDV
AZURE-1 and AZURE-4 Phase III studies met their 24-week primary endpoint versus delayed therapy, with rapid viral suppression and ALT normalization; responses continued to deepen in follow-up through 96 weeks.
Phase IIa extension data through 108 weeks showed 100% ALT normalization, 100% virologic response and >70% TND; tolerability was also described as favorable.
Management raised brelovitug’s projected opportunity to >$1B from $750M, driven by a higher-than-assumed Hepcludex price; the estimate includes competitive assumptions, with market share still uncertain.
Claims data identified ~15,000 diagnosed, insured patients under physician care as a baseline; broader reflex testing could expand identification beyond that pool.
The planned sales-force expansion includes ~40 representatives for adult PFIC, brelovitug and volixibat, expected to be in place by year-end 2026.
Latest events from Mirum Pharmaceuticals
- 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 - Sales growth lifted FY26 guidance as launches and late-stage programs advanced.MIRM
Q3 2026 - 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