Mirum Pharmaceuticals Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Mirum Pharmaceuticals, Inc. (Nasdaq: MIRM) announced the grant of non-qualified stock options for 118,800 shares to 10 new employees on April 12, 2021. The exercise price is set at $18.18 per share, which aligns with the closing trading price on the same day. The options will vest over four years, contingent on employment status. Mirum is advancing its late-stage pipeline, including maralixibat for Alagille syndrome, with an NDA under priority review by the FDA, and a marketing application validated by the European Medicines Agency for pediatric PFIC2.
- Grant of stock options may attract and retain talent, boosting company performance.
- Maralixibat's NDA is under priority review by the FDA, potentially expediting market entry.
- Validation of marketing application by the European Medicines Agency for pediatric PFIC2 enhances market opportunities.
- None.
Mirum Pharmaceuticals, Inc. (Nasdaq: MIRM) today announced that on April 12, 2021, the Compensation Committee of Mirum’s Board of Directors granted non-qualified stock option awards to purchase an aggregate of 118,800 shares of common stock to 10 new employees under Mirum’s 2020 Inducement Plan. The Compensation Committee of Mirum’s Board of Directors approved the awards as an inducement material to the new employees’ employment in accordance with Nasdaq Listing Rule 5635(c)(4).
Each stock option has an exercise price per share equal to
About Mirum
Mirum Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company focused on the development and commercialization of a late-stage pipeline of novel therapies for debilitating liver diseases. Mirum’s lead product candidate, maralixibat, is an investigational oral drug in development for Alagille syndrome (ALGS), progressive familial intrahepatic cholestasis (PFIC), and biliary atresia. Mirum has submitted an NDA for maralixibat in the treatment of cholestatic pruritus in patients with ALGS. The NDA has been accepted for priority review by the FDA with a PDUFA action date of September 29, 2021. Additionally, Mirum’s marketing authorization application for the treatment of pediatric patients with PFIC2 has been accepted for review (validated) by the European Medicines Agency.
Mirum is also developing volixibat, also an oral ASBT-inhibitor, in primary sclerosing cholangitis, intrahepatic cholestasis of pregnancy, and primary biliary cholangitis. For more information, visit MirumPharma.com.
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