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Mirum Pharmaceuticals MIRM offering, convertible notes and lawsuit news

Top story · Sep 8, 2026 · SEC filing 8-K

Mirum Pharmaceuticals reports a leadership change

(the “Company”) announced that, on September 2, 2026, the Company’s Board of Directors appointed Rob Myers, M.D., to succeed Joanne Quan, M.D., as the Company’s Chief Medical Officer, effective upon Dr.

Source: 8-K filed Sep 8, 2026 on SEC EDGAR

The world Mirum works in, not its own labs. Credits in the footer.
Ticker
MIRM
Listing
NASDAQ, United States
Next date
Q4 2026
Chief executive
Chris Peetz

Desk view · Opinion · Updated Oct 22, 2026

Mirum widens beyond Livmarli with a new approval and two phase 3 wins

Mirum has a growing commercial base and a run of positive late-stage data, with a new approval in September and 2026 sales guidance of $680 million to $700 million. The open issue is volixibat, where the FDA recommended a phase 3 study, and whether spending on trials and launches outpaces sales.

Read the full desk view

aibio.space Investor Rank · Opinion

8/10 Positive view

A growing rare liver franchise with a new approval and two phase 3 wins, though spending still exceeds sales and volixibat needs a phase 3 study.

Technology
2/2
Odds
2/2
Balance sheet
1/2
Risk
1/2
Momentum
2/2

Opinion only. The Investor Rank is aibio.space's opinion of the company's business position, drawn from the public sources on this page. It is not a recommendation to buy, sell or hold any security and it is not investment advice. It does not consider the share price, valuation or your circumstances, and it can change at any time. Payments from companies never affect it. How the rank works.

Technology
Proven in rare liver disease. Livmarli is approved and growing, and Mirum is extending the same bile acid transporter approach and adding an antibody for hepatitis delta.
Odds
Strong recent data. EXPAND and AZURE-1 both met primary endpoints, and Atebrioz was approved, but the FDA recommended a phase 3 study for volixibat in PSC.
Balance sheet
Better after refinancing. Cash was $561.3 million at June 30, 2026, helped by $690.0 million of zero-coupon converts, though operating expenses still exceed sales.
Main risk
Volixibat timing and concentration. Livmarli makes up most sales, and volixibat now faces a phase 3 recommendation from the FDA.
Watch next
Late 2026 readouts. AZURE-4 topline in the fourth quarter and the October launch of Atebrioz.

Top news on Mirum

  1. Legal

    Mirum sues Sandoz, Hetero, Biophore and Zydus in Delaware over generic Livmarli; trial set for 2028

    Mirum, Satiogen and Shire Human Genetic Therapies are plaintiffs in four consolidated cases. A 30-month FDA stay runs through March 29, 2029, and the Markman hearing is April 21, 2027.

  2. Debt Financing

    Mirum prices $600 million of 0% convertible notes and refinances 2029 debt

    The notes carry no interest and convert at about $138.94 a share, a 30% premium to the May 12 price. Mirum swapped $237.2 million of 4% notes due 2029 for cash and shares.

  3. Debt Financing

    Mirum proposes $600.0 million convertible notes offering

    Mirum plans to sell $600.0 million of convertible senior notes due 2032, with an option for up to $90.0 million more. Part of the proceeds would go toward exchanges of its 2029 notes.

Questions investors ask

What is aibio.space's Investor Rank for Mirum Pharmaceuticals?

8 out of 10, our positive view. A growing rare liver franchise with a new approval and two phase 3 wins, though spending still exceeds sales and volixibat needs a phase 3 study. This is opinion only, not a recommendation to buy, sell or hold, and it does not consider the share price or valuation. Source

What did the FDA approve for Mirum in September 2026?

On Sept. 25, 2026 the FDA approved Atebrioz (zilurgisertib), a once-daily oral ALK2 inhibitor, to reduce new heterotopic ossification in patients 12 and older with FOP. Incyte developed it and licensed it to Mirum. Source

What is Mirum's 2026 sales guidance?

Mirum raised its 2026 net product sales guidance to $680 million to $700 million on Aug. 5, 2026, after second-quarter net product sales of $176.2 million. Source

What were the AZURE-1 phase 3 results for brelovitug?

At week 24, 56% of hepatitis delta patients on 300 mg weekly and 45% on 900 mg every four weeks met the combined virologic and ALT endpoint, versus 0% on delayed treatment (p<0.0001). Source

Did the EXPAND trial of Livmarli succeed?

Yes. The phase 3 EXPAND study met its primary endpoint and all five prespecified secondary endpoints, and Mirum plans a supplemental U.S. application in the first half of 2027. Source

What did the FDA say about volixibat in PSC?

The FDA granted volixibat Breakthrough Therapy designation, but at a pre-NDA meeting it recommended conducting a phase 3 study. Mirum plans more discussions and targets a possible NDA in the first half of 2027. Source

What is the latest Mirum Pharmaceuticals (MIRM) stock news?

Our latest story on Mirum Pharmaceuticals, dated Aug 5, 2026: "Mirum sues Sandoz, Hetero, Biophore and Zydus in Delaware over generic Livmarli; trial set for 2028". Mirum, Satiogen and Shire Human Genetic Therapies are plaintiffs in four consolidated cases. A 30-month FDA stay runs through March 29, 2029, and the Markman hearing is April 21, 2027. Source

Does Mirum Pharmaceuticals have debt, a term loan or convertible notes?

Our latest debt story, dated May 12, 2026: "Mirum prices $600 million of 0% convertible notes and refinances 2029 debt". The notes carry no interest and convert at about $138.94 a share, a 30% premium to the May 12 price. Mirum swapped $237.2 million of 4% notes due 2029 for cash and shares. Source

How much cash does Mirum Pharmaceuticals have?

From our story of May 12, 2026: Mirum had $391.4 million of cash and investments at the end of 2025. Source

Is Mirum Pharmaceuticals facing a lawsuit?

Our latest legal story, dated Aug 5, 2026: "Mirum sues Sandoz, Hetero, Biophore and Zydus in Delaware over generic Livmarli; trial set for 2028". Mirum, Satiogen and Shire Human Genetic Therapies are plaintiffs in four consolidated cases. A 30-month FDA stay runs through March 29, 2029, and the Markman hearing is April 21, 2027. Claims in lawsuits are allegations until a court rules. Source

What is Mirum Pharmaceuticals's market cap?

We do not publish live share prices. In its annual report, Mirum Pharmaceuticals, Inc. put the market value of shares held by non-affiliates (public float) at $2.30 billion as of Jun 30, 2025. Source

Is Mirum Pharmaceuticals a smaller reporting company?

SEC records list Mirum Pharmaceuticals, Inc.'s filer category as: Large accelerated filer. Source

Where is Mirum Pharmaceuticals headquartered?

SEC records list its business address as 989 EAST HILLSDALE BOULEVARD, SUITE 300, FOSTER CITY, CA, 94404. Source

When does Mirum Pharmaceuticals's fiscal year end?

Mirum Pharmaceuticals, Inc.'s fiscal year ends on December 31, per SEC records. Source

What did Mirum Pharmaceuticals last file with the SEC?

Its most recent filing in our record is an 8-K filed 2026-10-13. All of its filings are on SEC EDGAR. Source

Pipeline

ProgramIndicationStage
Livmarli (maralixibat)Cholestatic pruritus in ultra-rare cholestatic liver diseases incl. biliary atresia (EXPAND)Phase 3 met primary endpoint (Oct. 2026); supplemental NDA planned 1H 2027 Source
BrelovitugChronic hepatitis delta virus infectionPhase 3 AZURE-1 met primary endpoint (Sept. 2026); AZURE-4 topline Q4 2026 Source
Atebrioz (zilurgisertib)Fibrodysplasia ossificans progressiva (FOP), age 12 and olderFDA approved Sept. 25, 2026; EU application under review Source
VolixibatCholestatic pruritus in primary sclerosing cholangitis (PSC)Phase 2b VISTAS met primary endpoint; Breakthrough Therapy designation; NDA targeted 1H 2027 Source
Volixibat (VANTAGE)Cholestatic pruritus in primary biliary cholangitis (PBC)Phase 2b fully enrolled; data expected Q1 2027 Source

Stock chart

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SEC filings and registration

SEC name
Mirum Pharmaceuticals, Inc.
CIK
1759425
Industry (SIC)
Pharmaceutical Preparations (2834)
US tickers
MIRM (Nasdaq)
State or country of incorporation
DE
Fiscal year ends
December 31
Filer category
Large accelerated filer
Business address
989 EAST HILLSDALE BOULEVARD, SUITE 300, FOSTER CITY, CA, 94404
Phone
650-667-4085
Shares outstanding
64,932,203 as of 2026-07-31 (10-Q filed 2026-08-05)

Recent filings (8-K and 6-K are the company's own announcements)

  • 8-K filed 2026-10-13
  • 8-K filed 2026-09-28
  • 8-K filed 2026-09-08
  • 10-Q filed 2026-08-05
  • 8-K filed 2026-08-05
  • 8-K filed 2026-06-18
  • 8-K filed 2026-05-18
  • 10-Q filed 2026-05-06

Source: SEC EDGAR, retrieved October 23, 2026. Shares outstanding is the cover-page figure from the latest periodic report. The SEC does not publish share prices.

Who manages this page This page is managed by aibio.space. The company does not run, edit or pay for this page. News, desk views and Investor Ranks are written and managed independently by aibio.space under our editorial and analytical judgment. Opinion only, not investment advice. How we work · Terms · Request a correction

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