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SUPNNasdaq

SUPERNUS PHARMACEUTICALS, INC.

Biopharma developer (SEC filing verified)·Commercial·Rockville, MD, United States·CEO: Mr. Jack A. Khattar M.B.A.
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SUPN evidence brief

What we can confirm

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What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

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BioSniper AIPage evidence connected

Prepared research question

What matters most for SUPN—catalysts, financial risk and supporting evidence?

Run cited research

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BioSniper AI · SUPN

Supernus Pharmaceuticals is a commercial-stage biopharmaceutical company focused on developing and commercializing products for the central nervous system (CNS), with a portfolio of marketed drugs and a pipeline of late-stage candidates.

Key risk: Patent expirations for key products

8.2/10

BioSniper Score

Based on 6 of 6 signals

Market Cap

$2.54B

Cash Runway

214.6 mo

Financial data as of Jun 30, 2026.

Tracking 8 pipeline candidates · 16 clinical trials · 7 catalysts for SUPERNUS PHARMACEUTICALS, INC..

AI OverviewAI overview is shown in English only.

Supernus Pharmaceuticals is a commercial-stage biopharmaceutical company focused on developing and commercializing products for the central nervous system (CNS), with a portfolio of marketed drugs and a pipeline of late-stage candidates.

  • Reported total revenue of $219.1M and a net loss of -$58.4M for the six months ended June 30, 2026 [sec].
  • Cash, cash equivalents, and marketable securities totaled $372.1M as of June 30, 2026, expected to fund operations for at least the next twelve months [sec_mda].
  • Qelbree prescriptions grew 17% year-over-year in Q2 2026, with adult prescriptions up 25% and pediatric up 14% [sec_mda].
  • GOCOVRI net sales increased 2% to $37.6M in Q2 2026, with total prescriptions growing 9% year-over-year [sec_mda].
  • Phase 2b study of SPN-817 for treatment-resistant focal seizures is ongoing with targeted enrollment of ~258 patients [sec_mda].

What works

  • Strong commercial product portfolio with growing prescription trends for Qelbree (17% increase) and GOCOVRI (9% increase) in Q2 2026 [sec_mda].
  • Solid cash position of $372.1M as of June 30, 2026, providing runway for operations and pipeline investment [sec_mda].
  • Diversified pipeline with multiple CNS candidates (SPN-812, SPN-817, SPN-820/821) targeting large markets like ADHD and epilepsy [sec].

What to weigh

  • Reported a net loss of -$58.4M for the first half of 2026, indicating ongoing profitability challenges [sec].
  • Significant patent expirations approaching for key products: OXTELLAR XR (2027), ONAPGO (2028), TROKENDI XR (2028), XADAGO (2031) [catalyst].
  • Pipeline candidates are still in clinical development with no guarantee of FDA approval; SPN-817 Phase 2b is ongoing and SPN-820/821 are in earlier stages [sec_mda].
  • Cash generation is highly dependent on commercial product success and FDA approvals, creating variability in future profitability [sec_mda].

From the filings

Quoted directly from source documents.

  • Qelbree prescription growth in Q2 2026

    elbree were 264,545 for the second quarter 2026, representing an increase of 17% compared to the same period last year.

    SEC MD&A · August 3, 2026

  • Cash and marketable securities position as of June 30, 2026

    securities, which totaled $372.1 million as of June 30, 2026, along with cash generated from ongoing operations and continued access to debt markets, will be sufficient to satisfy its cash requirements over the next twelve months and beyond.

    SEC MD&A · August 3, 2026

  • GOCOVRI sales and prescription growth in Q2 2026

    Net sales of GOCOVRI increased 2% to $37.6 million in the second quarter of 2026, compared to the same period in 2025. Total number of prescriptions grew by 9% in the second quarter of 2026 compared to the same period last year.

    SEC MD&A · August 3, 2026

Catalyst timeline

  • 2026-09-01 · Phase3_Topline · attention-deficit — Phase 3 Topline: Open-Label Extension Study to Evaluate the Long Term Safety and Efficacy of SPN-812 for the TreatmenTopline data from this study will inform the safety and efficacy profile of SPN-812 for ADHD.
  • 2027-04-13 · Patent_Expiry · OXTELLAR XR — Patent/Exclusivity Expiry: OXTELLAR XRExpiration could allow generic competition, impacting OXTELLAR XR revenue.
  • 2028-02-03 · Patent_Expiry · ONAPGO — Patent/Exclusivity Expiry: ONAPGOPatent expiry may open ONAPGO to generic entry.
  • 2028-04-04 · Patent_Expiry · TROKENDI XR — Patent/Exclusivity Expiry: TROKENDI XRPatent expiry could lead to generic competition for TROKENDI XR.
  • 2031-03-21 · Patent_Expiry · XADAGO — Patent/Exclusivity Expiry: XADAGOPatent expiry may affect XADAGO market exclusivity.
  • 2035-04-02 · Patent_Expiry · QELBREE — Patent/Exclusivity Expiry: QELBREELonger exclusivity for Qelbree, a key growth product.
  • 2038-08-23 · Patent_Expiry · GOCOVRI — Patent/Exclusivity Expiry: GOCOVRIExtended patent protection for GOCOVRI supports long-term revenue.
Risks & what to watch (4)

Key risks

  • Patent expirations for key productsOXTELLAR XR patent expires in 2027, ONAPGO in 2028, TROKENDI XR in 2028, XADAGO in 2031, exposing revenue to generic competition [catalyst].
  • Pipeline development riskSPN-817 Phase 2b is ongoing; SPN-820/821 are in earlier stages; failure or delay could impair long-term growth prospects [sec_mda].
  • Profitability variabilityCompany expects significant year-to-year profit variability due to market conditions and R&D investments; net loss of -$58.4M in H1 2026 [sec_mda].
  • Dependence on commercial successCash generation is highly dependent on product sales and FDA approvals; any decline could strain liquidity [sec_mda].

What to watch

  • Phase 3 topline data for SPN-812 open-label extension study expected September 1, 2026 [catalyst].
  • Progress of SPN-817 Phase 2b study for treatment-resistant focal seizures [sec_mda].
  • Revenue and prescription trends for Qelbree and GOCOVRI in upcoming quarters [sec_mda].
  • Any updates on SPN-820/821 pipeline development and regulatory milestones [sec].

Sources: Catalysts · SEC filings · SEC MD&A · Generated August 25, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 6 of 6 signals · derived from public data

Cash Runway10.0

214.6 months

Financial Health9.4

D/E 0.38 · 0% dilution

Pipeline Maturity10.0

Lead: Approved

Pipeline Breadth10.0

8 candidates

Catalyst Momentum10.0

7 upcoming, next in ~2d

Insider Signal0.0

0 buys · 15 sells (180d)

Runway

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

327

Total value held

$3.06B

Showing top 10 of 327 institutional holders of SUPERNUS PHARMACEUTICALS, INC.. Open the full 13F history after sign-in.

Short Interest

as of Apr 19, 2026
% of float
11.1%
Days to cover
7.3
Shares short
4,532,867
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

SUPN short interest

Governance

Frequently asked questions

What is the AI investment thesis for SUPERNUS PHARMACEUTICALS, INC.?

Supernus Pharmaceuticals is a commercial-stage biopharmaceutical company focused on developing and commercializing products for the central nervous system (CNS), with a portfolio of marketed drugs and a pipeline of late-stage candidates.

What is SUPERNUS PHARMACEUTICALS, INC.'s lead drug candidate?

SUPERNUS PHARMACEUTICALS, INC.'s most advanced tracked candidate is APOKYN (Approved) for Acute, intermittent treatment of hypomobility or "OFF" episodes in patients with advanced Parkinson's Disease.

What is SUPERNUS PHARMACEUTICALS, INC.'s next catalyst?

SUPERNUS PHARMACEUTICALS, INC.'s next tracked catalyst is a Phase3_Topline event — "Phase 3 Topline: Open-Label Extension Study to Evaluate the Long Term Safety and Efficacy of SPN-812 for the Treatmen" — expected September 1, 2026.

Who is the CEO of SUPERNUS PHARMACEUTICALS, INC.?

Mr. Jack A. Khattar M.B.A. is the chief executive officer of SUPERNUS PHARMACEUTICALS, INC. (SUPN).

Where is SUPERNUS PHARMACEUTICALS, INC. headquartered?

SUPERNUS PHARMACEUTICALS, INC. (SUPN) is headquartered in Rockville, MD, United States.

925 companies232,681 SEC filings21,417 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.