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Data updated: Jun 28, 2026

INTRA-CELLULAR

Pharma
NeurologyCardiovascular Execution: Fair

INTRA-CELLULAR is a pharmaceutical company focused on Neurology, Cardiovascular. Key products include CAPLYTA.

2019
Since
1
Drugs
-
Trials
0
New Drugs (2yr)
Modality:
1 Small Molecules

FDA Novel Drug Designations

(2019)
1 Novel 1 Fast Track
See 1 novel approval →
2019 CAPLYTA (LUMATEPERONE TOSYLATE) Fast Track

INTRA-CELLULAR at a Glance

  • Growing R&D activity with 12 trials in last 2 years
  • Fast trial execution (16 months median completion)

INTRA-CELLULAR's Key Drugs

INTRA-CELLULAR's core commercial portfolio centers on CAPLYTA, spanning Neurology and Cardiovascular — its most strategically important drugs approved in the last 15 years.

INTRA-CELLULAR's Recent FDA Approvals

New NDA/BLA approvals for INTRA-CELLULAR over the last two years — novel drugs only, excluding generics and label supplements.

No recent approvals

INTRA-CELLULAR's Therapeutic Areas

INTRA-CELLULAR's approved drugs and pipeline span 2 therapeutic areas, led by Neurology and Cardiovascular, across 0 biologic and 1 small-molecule drug. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Neurology 92%
0 drugs Phase 3: 1 Phase 2: 3 Phase 1: 2
Cardiovascular 8%
0 drugs Phase 1: 1

INTRA-CELLULAR's Top Competitors

INTRA-CELLULAR's closest competitors by therapeutic-area and drug-target overlap include GE HEALTHCARE, Novo Nordisk, and LEDERLE. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

INTRA-CELLULAR Pipeline Snapshot

INTRA-CELLULAR has 7 active clinical programs from ClinicalTrials.gov — 1 Phase 3, 3 Phase 2 and 3 Phase 1.

1
Phase 3
3
Phase 2
3
Phase 1

Pro Intelligence Preview

Deep insights for investors and analysts

Revenue Insights

  • CAPLYTA leads revenue
  • Drug-level revenue analysis
View revenue breakdown →

Trial Catalysts

  • Neurology pipeline focus
  • Phase 3 readout tracking
View full pipeline →

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: 10/18 completed
  • Speed: 16 months avg
Unlock Full Intelligence

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