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Mirum Pharmaceuticals, Inc. logo

Mirum Pharmaceuticals, Inc.

MIRM
NASDAQ: MIRM Delayed
94.25USD 0.3%
As of 6 June 2026, Mirum Pharmaceuticals, Inc. has a market cap of $5.75B USD, ranking #3402 globally and #1014 in the United States. It ranks #251 in the Healthcare sector, and #97 in the Drug Manufacturers - General industry.
Global Rank
3402
Country Rank
1014
Sector Rank
251
Industry Rank
97
Key Stats
Market Cap
$5.75BUSD
Enterprise Value
$5.68BUSD
Revenue (TTM)
$521.31MUSD
EBITDA (TTM)
$2.11MUSD
Net Income (TTM)
-$23.36MUSD
EBITDA Margin
0.4%
Profit Margin
-4.5%
PS Ratio
11.0
PB Ratio
15.5
EV/EBITDA
2695.8
Company Profile
Country (HQ)
Sector
Healthcare
Industry
Drug Manufacturers - General
CEO
Christopher Peetz open_in_new
Employees
372
Founded
2018
IPO
18 Jul 2019
Website
mirumpharma.com open_in_new
1d 1w 1m 3m 6m 1y
0.3% -0.1% 6.6% -6.5% 34% 128%

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Markets

Exchange Ticker Price
NASDAQ
MIC: XNAS
PRIMARY
MIRM
Mirum Pharmaceuticals Inc
ISIN: US6047491013
Shares Out.:
60.981M1 Shares Float: 49.588M2
TV:
SA:
YF:
GF:
NQ:
BA:
MS:
94.25 USD
Frankfurt Stock Exchange
MIC: XFRA
08D
Mirum Pharmaceuticals Inc
ISIN: US6047491013
TV:
SA:
YF:
GF:
BA:
08D
MS:
77.32 EUR
Mexican Bolsa
MIC: XMEX
MIRM
Mirum Pharmaceuticals Inc
ISIN: US6047491013
Shares Out.:
50.238M1 Shares Float: 40.642M2
TV:
SA:
YF:
GF:
BA:
MS:
1,256.12 MXN
1Market cap is calculated using shares outstanding.
2Float shares are publicly tradable shares, excluding insider-held stock.

About Mirum Pharmaceuticals, Inc.

Mirum Pharmaceuticals, Inc., a biopharmaceutical company, focuses on the development and commercialization of novel therapies for debilitating rare and orphan diseases. Its lead product candidate is LIVMARLI (maralixibat), an orally administered and minimally absorbed ileal bile acid transporter (IBAT) inhibitor that is approved for the treatment of cholestatic pruritus in patients with Alagille syndrome in the United States and internationally. The company is also involved in the commercialization of Cholbam, a cholic acid capsule, which is approved as treatment for pediatric and adult patients with bile acid synthesis disorders due to single enzyme defects and for adjunctive treatment of patients with peroxisomal disorders, including peroxisome biogenesis disorder-Zellweger spectrum disorder and Smith-Lemli-Opitz syndrome; and Chenodal, a tablet, which is approved for the treatment of radiolucent stones in the gallbladder, and under development for the treatment cerebrotendinous xanthomatosis. In addition, it develops Volixibat, an oral and minimally absorbed agent designed to inhibit IBAT, currently under Phase 2b clinical trial for the treatment of adult patients with cholestatic liver diseases; Brelovitug, for the treatment of chronic HDV infection, which is in Phase 2 clinical trial; and MRM-3379, that is in Phase 2 clinical study for the treatment of FXS. The company has a collaboration agreement with the Shire International GmbH; License Agreement with Pfizer Inc.; Sanofi-Aventis Deutschland GmbH; Novartis Pharma AG; Lonza Ltd.; Enthorin Therapeutics, LLC and Dart Neuroscience LLC; Asset Purchase Agreement with Asklepion Pharmaceuticals, LLC; License and Manufacturing Agreement with LGM Pharma; and Asset Purchase Agreement with Travere Therapeutics, Inc. The company was incorporated in 2018 and is headquartered in Foster City, California.

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