Baker Bros. Advisors Adds $52M in Mirum Pharmaceuticals, Inc. ($MIRM)

Editorial illustration for Mirum Pharmaceuticals, Inc. (MIRM)

Key Points

  • Wall Street's consensus rating on $MIRM is Strong Buy and an average price target of $138.21.
  • $MIRM last traded around $117.07.

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Baker Bros. Advisors acquired a new position in Mirum Pharmaceuticals, Inc. ($MIRM), according to its most recent Form 13F filing with the Securities and Exchange Commission. The fund owned 445,975 shares of Mirum Pharmaceuticals, Inc.. Baker Bros. Advisors's holdings in Mirum Pharmaceuticals, Inc. were worth $52.21 million as of its most recent filing.

Mirum Pharmaceuticals, Inc. Stock Up 20.1%

Shares of Mirum Pharmaceuticals, Inc. ($MIRM) traded around $117.07 on Saturday, up 20.1% for the day.

Last price$117.07
Market cap$5.98B
Forward P/E-282.83
Beta0.51
52-week low$63.23
52-week high$130
50-day MA$110.09
200-day MA$95.48
Current ratio2.86
Quick ratio2.62

Mirum Pharmaceuticals, Inc. Earnings

EPS (ttm)-$14.08
Revenue (ttm)$618.07M
Revenue growth37.90%
Net margin-139.18%
Return on equity-702.97%
Next earningsNov 4, 2026

Analysts Set New Price Targets

ConsensusStrong Buy
Average target$138.21
High target$183
Low target$118
Analysts covering14

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.

ExchangeNasdaqGM
SectorHealthcare
IndustryBiotechnology
HeadquartersFoster City, CA
CEOMr. Christopher Peetz
Employees433

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