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Data updated: Jun 28, 2026

SUPERNUS PHARMS

Specialty
NeurologyDermatology Execution: Good

SUPERNUS PHARMS is a specialty pharmaceutical company focused on Neurology, Dermatology. Key products include TROKENDI XR.

2012
Since
5
Drugs
-
Trials
0
New Drugs (2yr)
Modality:
4 Small Molecules

FDA Novel Drug Designations

(2021)
1 Novel
See 1 novel approval →
2021 QELBREE (VILOXAZINE HYDROCHLORIDE)

SUPERNUS PHARMS at a Glance

  • Fast trial execution (14 months median completion)

SUPERNUS PHARMS's Key Drugs

SUPERNUS PHARMS's core commercial portfolio centers on TROKENDI XR, GOCOVRI, OXTELLAR XR, spanning Neurology and Dermatology — its most strategically important drugs approved in the last 15 years.

SUPERNUS PHARMS's Recent FDA Approvals

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

No recent approvals

SUPERNUS PHARMS's Therapeutic Areas

SUPERNUS PHARMS's approved drugs and pipeline span 2 therapeutic areas, led by Neurology and Dermatology, across 0 biologic and 4 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Neurology 75%
3 drugs
Dermatology 25%
1 drugs

SUPERNUS PHARMS's Top Competitors

SUPERNUS PHARMS's closest competitors by therapeutic-area and drug-target overlap include Pfizer, Eli Lilly, and PAI HOLDINGS PHARM. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

SUPERNUS PHARMS Pipeline Snapshot

Active clinical trials for SUPERNUS PHARMS across all therapeutic areas, from ClinicalTrials.gov.

No active pipeline data available

Phase 3 Readout Calendar Pro

1 Phase 3 trial with confidence-graded primary completion dates.

Full calendar →
Q3 2026
SPN-812
Attention-Deficit/Hyperactivity Disorder
Estimated · stale NCT02736656

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

  • TROKENDI XR leads revenue
  • 4 key drugs tracked
View revenue breakdown →

Trial Catalysts

  • Neurology pipeline focus
  • 1 Phase 3 readout 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: 14/19 completed
  • Speed: 14 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