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XENE

Xenon Pharmaceuticals Inc.

Pharmaceutical preparations·Phase 3·Burnaby, BC, Canada·CEO: Mr. Ian C. Mortimer C.M.A., CPA, M.B.A.
NeurologyPsychiatry

XENE evidence brief

What we can confirm

BioSniper Score:
5.5 / 10
Market Cap:
$5.63B
Lead Asset:
xen1101 (Phase 2)

What it means

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

What to watch

Market Cap: $5.63B · Lead Asset: xen1101 (Phase 2)
BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · XENE

Xenon Pharmaceuticals Inc. (XENE) is a neuroscience-focused biopharmaceutical company advancing clinical-stage programs in epilepsy, major depressive disorder, and bipolar disorder, with its lead asset azetukalner in Phase 3 trials.

Key risk: Pre-revenue stage

5.5/10

BioSniper Score

Based on 4 of 6 signals

Market Cap

$5.63B

Cash Runway

—

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 1 pipeline candidate · 14 clinical trials for Xenon Pharmaceuticals Inc..

Similar companies

AI OverviewAI overview is shown in English only.

Xenon Pharmaceuticals Inc. (XENE) is a neuroscience-focused biopharmaceutical company advancing clinical-stage programs in epilepsy, major depressive disorder, and bipolar disorder, with its lead asset azetukalner in Phase 3 trials.

  • Lead asset azetukalner is in Phase 3 trials for focal onset seizures (X-TOLE2, X-TOLE3), primary generalized tonic-clonic seizures (X-ACKT), major depressive disorder (X-NOVA2, X-NOVA3), and bipolar disorder (X-CEED) [sec_mda · as of 2026-08-06].
  • Positive topline Phase 3 X-TOLE2 data in focal onset seizures was announced on March 9, 2026, supporting a planned FDA NDA submission in Q3 2026 [news · published 2026-05-11].
  • Cash & equivalents of $119.5M as of 2026-06-30, with shareholders' equity of $1,242.4M and net income of -$110.7M for the quarter [latest reported financials].
  • Accumulated deficit of $1,458.4 million as of 2026-08-06, primarily from R&D and general/administrative costs [sec_mda · as of 2026-08-06].
  • Enrollment is ongoing in multiple Phase 3 studies, with topline data from X-NOVA2 (MDD) expected in H1 2027 [sec_mda · as of 2026-08-06].

What works

  • Positive Phase 3 X-TOLE2 topline data in focal onset seizures announced March 9, 2026, supporting a planned FDA NDA submission in Q3 2026 [news · published 2026-05-11].
  • Multiple Phase 3 programs are advancing across epilepsy, MDD, and BPD, indicating a broad pipeline [sec_mda · as of 2026-08-06].
  • Company expects existing cash and marketable securities to fund operating expenses for at least the next 12 months as of 2026-08-06 [sec_mda · as of 2026-08-06].
  • Mechanistic data suggests azetukalner may offer additive benefits in combination with commonly used anti-seizure medications [news · published 2026-08-28].

What to weigh

  • Net loss of $110.7M for the quarter ended 2026-06-30, with accumulated deficit of $1,458.4M as of 2026-08-06 [latest reported financials; sec_mda · as of 2026-08-06].
  • No revenue reported as of 2026-06-30, indicating the company is pre-commercial [latest reported financials].
  • Operating expenses are expected to increase substantially as the company prepares for potential commercial launch and further development [sec_mda · as of 2026-08-06].
  • Cash & equivalents of $119.5M as of 2026-06-30, a significant drop from the $1.34B in cash and marketable securities reported at end of Q1 2026 [latest reported financials; news · published 2026-05-11].

From the filings

Quoted directly from source documents.

  • Positive Phase 3 X-TOLE2 topline data announced March 9, 2026

    “positive topline data announced on March 9, 2026”

    SEC filings · April 22, 2026

  • Planned FDA NDA submission in Q3 2026

    “supporting a planned FDA New Drug Application submission in the third quarter of 2026”

    News · May 11, 2026

  • Accumulated deficit of $1,458.4 million as of 2026-08-06

    “we had an accumulated deficit of $1,458.4 million”

    SEC MD&A · August 6, 2026

Risks & what to watch (4)›

Key risks

  • Pre-revenue stage — No revenue reported as of 2026-06-30; company depends on financing to fund operations [latest reported financials].
  • High accumulated deficit — Accumulated deficit of $1,458.4M as of 2026-08-06, with net losses continuing [sec_mda · as of 2026-08-06].
  • Cash burn rate — Cash & equivalents dropped from ~$1.34B (Q1 2026) to $119.5M (Q2 2026), though equity remains high [news · published 2026-05-11; latest reported financials].
  • Clinical trial execution — Multiple Phase 3 trials ongoing; delays or negative data could impact timelines and funding [sec_mda · as of 2026-08-06].

What to watch

  • FDA NDA submission for azetukalner in focal onset seizures, planned for Q3 2026 [news · published 2026-05-11].
  • Topline data from Phase 3 X-NOVA2 (MDD) expected in H1 2027 [sec_mda · as of 2026-08-06].
  • Completion of enrollment in X-TOLE3 and X-ACKT epilepsy studies, with X-ACKT enrollment outside Japan expected to complete in 2026 [sec_mda · as of 2026-08-06].
  • Cash runway and potential need for additional financing given pre-revenue status and high operating expenses [sec_mda · as of 2026-08-06].

Sources: Catalysts · News · SEC filings · SEC MD&A · Generated October 6, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 4 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health9.9

D/E 0.04 · 0% dilution

Pipeline Maturity6.0

Lead: Phase 2

Pipeline Breadth3.3

1 candidate

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider Signal2.9

0 buys · 3 sells (180d)

Pipeline

Regulatory

Financials

Short Interest

as of Apr 30, 2026
% of float
5.0%
Days to cover
4.1
Shares short
4,854,352
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 →

XENE short interest

Governance

Frequently asked questions

What is the AI investment thesis for Xenon Pharmaceuticals Inc.?

Xenon Pharmaceuticals Inc. (XENE) is a neuroscience-focused biopharmaceutical company advancing clinical-stage programs in epilepsy, major depressive disorder, and bipolar disorder, with its lead asset azetukalner in Phase 3 trials.

What is Xenon Pharmaceuticals Inc.'s lead drug candidate?

Xenon Pharmaceuticals Inc.'s most advanced tracked candidate is xen1101 (Phase 2) for Focal Epilepsy; Major Depressive Disorder; Focal Onset Seizures.

Who is the CEO of Xenon Pharmaceuticals Inc.?

Mr. Ian C. Mortimer C.M.A., CPA, M.B.A. is the chief executive officer of Xenon Pharmaceuticals Inc. (XENE).

Where is Xenon Pharmaceuticals Inc. headquartered?

Xenon Pharmaceuticals Inc. (XENE) is headquartered in Burnaby, BC, Canada.

What therapeutic areas does Xenon Pharmaceuticals Inc. focus on?

Xenon Pharmaceuticals Inc. develops therapies across Neurology, Psychiatry.

923 companies304,846 SEC filings22,720 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.