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NEUROCRINE BIOSCIENCES INC

Biological Products, (No Diagnostic Substances)·SAN DIEGO, CA·FY end 12/31·CIK 914475
OverviewFinancialsCompensationGovernanceInsidersFilings

Board of Directors

11 members · 10 independent · FY 2025
DirectorRoleTenureAgeCommitteesIndep.Annual fees
William H. Rastetter, Ph.D.Chair16y77Tech
Kyle W. Gano, Ph.D.CEO and Director2y53
George J. MorrowDirector11y74NCGComp
Leslie V. NorwalkDirector7y60NCG
Christine A. PoonDirector3y73NCGAudit
Richard F. PopsDirector28y64TechComp
Shalini SharpDirector6y51CompAudit
Stephen A. Sherwin, M.D.Director27y77TechAudit
Kevin C. Gorman, Ph.D.Director18y68Tech
Gary A. LyonsDirector33y74Tech
Johanna MercierDirector5y56

Risk-factor diff

FY 2025 10-K vs. FY 2024
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Net-new paragraphs in the most recent 10-K's Item 1A. Companies rarely add risk language without a real reason — additions here are often a leading signal of management concerns.

NEW · FY 2025

Neurocrine Biosciences is a neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing, and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine, and immunological disorders.

NEW · FY 2025

Our portfolio of products includes U.S. Food and Drug Administration (FDA) approved treatments for tardive dyskinesia (TD), chorea associated with Huntington's disease, classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (CAH), and endometriosis and uterine fibroids in collaboration with AbbVie Inc. (AbbVie). In addition, we have a diversified portfolio of multiple compounds in mid- to late-phase development across our core therapeutic areas and an expanding early-phase pipeline that includes a range of modalities including small molecules, peptides, proteins, antibodies, c…

NEW · FY 2025

(valbenazine) in the U.S. as the first FDA-approved drug for the treatment of TD in May 2017 and for the treatment of chorea associated with Huntington's disease in August 2023 and launched CRENESSITY

NEW · FY 2025

We estimate that TD affects approximately 800,000 people in the U.S., that approximately 90% of the 40,000 people in the U.S. affected by Huntington’s disease will develop chorea, and that CAH affects at least 20,000 people in the U.S. Key elements of our commercial strategy include maximizing the opportunities in INGREZZA and CRENESSITY through consistent and effective commercial execution, continued development of valbenazine as the best-in-class treatment for new patient populations, and to lead the evolving understanding of vesicular monoamine transporter 2 (VMAT2) biology and its role in …

NEW · FY 2025

Total net product sales for 2025 increased $503.3 million, or 21.6%, to $2.83 billion, reflecting increased net product sales of CRENESSITY, which was launched in the U.S. as a first-in-class FDA-approved treatment of CAH in December 2024, and INGREZZA, driven by record total prescriptions on strong patient demand, partially offset by a lower net price due to new market access investments to support long-term growth.

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Policies & disclosures

Clawback, anti-hedging, stock ownership, and related-party policies will populate from extracted proxy sections.