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Data updated: Jun 28, 2026

NEUROCRINE

Pharma

NEUROCRINE is a pharmaceutical company focused on Dermatology, Neurology, Gastroenterology. Key products include INGREZZA SPRINKLE.

2017
Since
3
Drugs
-
Trials
2
New Drugs (2yr)
Modality:
3 Small Molecules

FDA Novel Drug Designations

(2017-2024)
2 Novel 1 First-in-Class 1 Orphan 2 Breakthrough 2 Priority Review 2 Fast Track
See 2 novel approvals →
2024 CRENESSITY (CRINECERFONT) First-in-Class · Orphan · Breakthrough · Priority Review · Fast Track
2017 INGREZZA (VALBENAZINE TOSYLATE) Breakthrough · Priority Review · Fast Track

NEUROCRINE at a Glance

  • Fast trial execution (15 months median completion)

NEUROCRINE's Key Drugs

NEUROCRINE's core commercial portfolio centers on INGREZZA SPRINKLE, INGREZZA, CRENESSITY, spanning Dermatology and Neurology — its most strategically important drugs approved in the last 15 years.

NEUROCRINE's Recent FDA Approvals

NEUROCRINE secured 2 new FDA approvals for novel drugs (NDA/BLA) in the last two years.

NEUROCRINE's Therapeutic Areas

NEUROCRINE's approved drugs and pipeline span 3 therapeutic areas, led by Dermatology and Neurology, across 0 biologic and 3 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Dermatology 82%
2 drugs Phase 3: 4 Phase 2: 5 Phase 1: 4
Neurology 16%
0 drugs Phase 2: 2 Phase 1: 4
Gastroenterology 2%
0 drugs Phase 1: 1

NEUROCRINE's Top Competitors

NEUROCRINE's closest competitors by therapeutic-area and drug-target overlap include Pfizer, Eli Lilly, and Bristol-Myers Squibb. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

NEUROCRINE Pipeline Snapshot

NEUROCRINE has 20 active clinical programs from ClinicalTrials.gov — 4 Phase 3, 7 Phase 2 and 9 Phase 1.

4
Phase 3
7
Phase 2
9
Phase 1

Phase 3 Readout Calendar Pro

8 Phase 3 trials with confidence-graded primary completion dates.

Full calendar →
Q3 2027
NBI-1065845
Major Depressive Disorder
Estimated · fresh NCT06963021
Q3 2027
NBI-1065845
Major Depressive Disorder
Estimated · aging NCT06911112
Q3 2027
NBI-1065845
Major Depressive Disorder
Estimated · aging NCT06786624
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Anchored on CT.gov primary completion date. Topline announcements typically precede this by 3–9 months. Confidence labels combine date type (ACTUAL/ESTIMATED) with last-update freshness.

Pro Intelligence Preview

Deep insights for investors and analysts

Revenue Insights

  • INGREZZA SPRINKLE leads revenue
  • 3 key drugs tracked
View revenue breakdown →

Trial Catalysts

  • Dermatology pipeline focus
  • 8 Phase 3 readouts tracked
View readout calendar →

Patent Risk

  • Patent expiration timeline
  • Revenue at risk analysis
View patent timeline →

Compare Companies

  • Side-by-side pipeline analysis
  • Revenue & market share comparison
Compare with competitor →

Execution Intelligence

  • Phase 3: 6/20 completed
  • Speed: 15 months avg
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Revenue forecasts • Trial milestones • Patent risk modeling

How We Calculate These Metrics

Execution Quality Score

Measures trial completion rates weighted by phase importance. Phase 3 trials count 4x more than Phase 1 because late-stage completion is harder and more valuable.

What counts as "completed": A trial that reached its planned endpoint and reported results. Trials that were terminated early, withdrawn, or suspended are not counted as completed—these often indicate safety issues, lack of efficacy, or strategic pivots.

  • Excellent (80%+): Top-tier execution, most trials reach planned endpoints
  • Good (60-79%): Strong execution with occasional early terminations
  • Fair (40-59%): Average execution, notable rate of terminated/withdrawn trials
  • Needs Improvement (under 40%): High termination rates, execution challenges