Mirum Pharmaceuticals Q2 Results: Earnings call set for Aug 5, 2026
Mirum Pharmaceuticals Inc is set to release its Q2 2026 earnings on August 5, 2026, accompanied by a conference call at 4:30 p.m. ET. The rare disease firm will discuss financial outcomes and corporate updates, with access available via dial-in or webcast. The company continues to advance its commercial portfolio including LIVMARLI and CHOLBAM, alongside a robust pipeline targeting rare liver and genetic conditions.

*this image is generated using AI for illustrative purposes only.
Mirum Pharmaceuticals Inc (NASDAQ: MIRM) will announce its second quarter 2026 financial results on August 5, 2026. The rare disease company will also host a conference call to discuss the quarterly figures and recent corporate progress. This update provides investors with timely insight into the company’s operational and financial trajectory for the period ending June 30, 2026.
The conference call is scheduled for Wednesday, August 5, 2026, at 4:30 p.m. ET / 1:30 p.m. PT. Participants can join via dial-in or webcast.
| Access Method | Details |
|---|---|
| US/Toll-Free | + 1 833 461 5787 |
| International | +1 585 542 9983 |
| Access Code | 789239699 |
| Webcast | Available via Mirum’s corporate website Investors section |
An archived webcast of the event will be available for replay following the conclusion of the live broadcast.
Mirum Pharmaceuticals operates as a leading rare disease company with a global footprint of approved products and a broad pipeline of investigational medicines. The company focuses on rare liver and rare genetic diseases, leveraging deep expertise and strong connections to patient communities. Its commercial portfolio includes LIVMARLI (maralixibat) for Alagille syndrome (ALGS) and progressive familial intrahepatic cholestasis (PFIC), CHOLBAM (cholic acid) for bile-acid synthesis disorders, and CTEXLI (chenodiol) for cerebrotendinous xanthomatosis (CTX).
The company’s clinical-stage pipeline features several late-stage candidates. These include volixibat, an IBAT inhibitor for primary sclerosing cholangitis (PSC) and primary biliary cholangitis (PBC); brelovitug, a fully human monoclonal antibody for chronic hepatitis delta virus (HDV); zilurgisertib, an ALK2 inhibitor under regulatory review with the FDA for fibrodysplasia ossificans progressiva (FOP); and MRM-3379, a PDE4D inhibitor being evaluated for Fragile X syndrome (FXS).
How might the Q2 2026 revenue performance of LIVMARLI and CHOLBAM influence Mirum's cash runway ahead of potential commercialization for volixibat?
What specific guidance will management provide regarding the timeline for FDA approval decisions on zilurgisertib for fibrodysplasia ossificans progressiva (FOP)?
Will the conference call address any updates on the Phase 3 trial data for volixibat in primary sclerosing cholangitis (PSC) or primary biliary cholangitis (PBC)?






























