Mirum Pharmaceuticals (MIRM) Q4 2024 earnings summary
Event summary combining transcript, slides, and related documents.
Q4 2024 earnings summary
8 Jul, 2026Executive summary
Achieved 2024 net product sales of $336.4 million, up from $178.9 million in 2023, reflecting strong commercial growth across all three approved ultra-rare disease medicines and a robust pipeline with expanding patient populations.
Global commercial reach with LIVMARLI expanded to 30 countries, including major European markets, and a pipeline targeting multi-billion dollar orphan indications in hepatology, GI, and rare genetic neurology.
Portfolio includes LIVMARLI, CHOLBAM, and CTEXLI, with four additional indications in development and significant progress in 2024 through new approvals, label expansions, and pipeline advancements.
Strategic priorities include global expansion of commercial medicines, advancing pipeline assets, selective product acquisitions, and maintaining financial discipline.
2025 net product sales guidance is $420–$435 million, with continued positive cash flow expected and a $293 million cash balance at FY2024.
Financial highlights
2024 net product sales reached $336.4 million, up from $178.9 million in 2023; Q4 2024 net product sales were $99.4 million, a 43% year-over-year increase.
LIVMARLI 2024 net product sales were $213.3 million, a 50% increase over 2023; Bile acid medicines generated $123.1 million in 2024 sales.
Total operating expenses for 2024 were $424.5 million, including R&D of $140.6 million and SG&A of $202.2 million.
Net loss for 2024 was $87.9 million, improved from $163.4 million in 2023; operating loss was $87.6 million, improved from $109.2 million in 2023.
Ended 2024 with $293 million in cash, cash equivalents, and investments, up from $286.3 million at year-end 2023.
Outlook and guidance
2025 net product sales are projected between $420 million and $435 million, with positive cash flow anticipated.
Key milestones for 2025–2026 include completion of VISTAS (PSC) and VANTAGE (PBC) trial enrollments, and initiation of MRM-3379 Phase 2 study in Fragile X Syndrome.
VISTAS study for volixibat in PSC to complete enrollment in H2 2025; topline data expected 2026.
VANTAGE study in PBC and LIVMARLI EXPAND Phase 3 study expected to complete enrollment in 2026.
Anticipate adding close to $100 million to the top line in 2025.
Latest events from Mirum Pharmaceuticals
- Multiple late-stage data readouts and launches set the stage for rare disease market expansion.MIRM
Morgan Stanley 24th Annual Global Healthcare Conference - Commercial growth, pipeline catalysts, and global expansion position the business for continued momentum.MIRM
H.C. Wainwright 28th Annual Global Investment Conference - Key clinical milestones and regulatory filings for rare disease therapies expected in the next year.MIRM
Citigroup’s Biopharma Back to School Summit 2026 - Multiple late-stage catalysts and commercial expansion set the stage for significant financial growth.MIRM
12th Annual Cantor Fitzgerald Global Healthcare Conference - Multiple late-stage rare disease assets drive projected $680–700M sales in 2026.MIRM
Corporate presentation - Q2 2026 sales rose 38% to $176.2M, guidance raised, and pipeline advanced.MIRM
Q2 2026 - Robust sales growth and a rich late-stage pipeline position the company for five potential approvals by 2027.MIRM
Corporate presentation - Q2 2024 sales jumped 139% to $77.8M, with narrowed net loss and strong pipeline progress.MIRM
Q2 2024 - Volixibat Phase IIb interim results show rapid, significant itch reduction and strong safety in PSC and PBC.MIRM
Study Result