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Xenon Pharmaceuticals Inc

Xenon Pharmaceuticals Inc. is a neuroscience-focused biopharmaceutical company that discovers, develops, and delivers therapeutics for neurological and psychiatric disorders. Its lead candidate, Azetukalner, is a novel, potent Kv7 potassium channel opener in Phase 3 clinical development for epilepsy, including focal onset seizures and primary generalized tonic-clonic seizures, as well as neuropsychiatric disorders such as major depressive disorder and bipolar depression. The company's Phase 1 Single Ascending Dose/Multiple Ascending Dose products include XEN1701 targeting the sodium channel and XEN1120 targeting the Kv7 potassium channel for pain. Xenon has a license and collaboration agreement with Neurocrine Biosciences, Inc. for the development of NBI-921355, a Nav1.2/1.6 sodium channel inhibitor in Phase 1 clinical trials for certain types of epilepsy. Incorporated in 1996, the company is headquartered in Burnaby, Canada.

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United States
Biotech & Genomic Medicine▼2

Steel Dynamics Falls on Weak Guidance, Xenon Plunges on Trial Enrollment Pause

Steel Dynamics issued weaker third-quarter earnings guidance, sending its shares down 4.1%. Xenon Pharmaceuticals announced it is temporarily pausing enrollment in its clinical studies for treatments for major and bipolar depression amid reports of side effects, and its shares plummeted 30.7%. Advanced Micro Devices rose 2.7% and Texas Instruments climbed 3.3%, both on the broader semiconductor rally.
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Biotech & Genomic Medicine › Neuroscience & Neurodegenerative ▼Regulation
Semiconductors › Logic, Compute & Connectivity Processors ▲Demand
STLD · Capital · Negative Issued weaker third-quarter earnings guidance, sending shares down 4.1%.
XENE · Technology · Negative Temporarily paused enrollment in clinical studies for depression treatments amid side-effect reports.
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United States
Biotech & Genomic Medicine▼impact 4

Xenon Pharmaceuticals Pauses Depression Trial Enrollment, Stock Sinks 31%

Xenon Pharmaceuticals paused enrollment in its Phase 3 psychiatry studies for major depressive disorder and bipolar disorder after higher rates of neuropsychiatric side effects, including confusion, somnolence, ataxia, and rare cases of psychosis. The company plans to adjust dosing through titration or lower doses to improve patient tolerance before resuming enrollment. Its X-NOVA2 trial for major depressive disorder had already enrolled 80% of its target 450 patients, with results still expected in Q1 2027, and Xenon will decide whether to resume the depression and bipolar trials after seeing those results. Needham cut its price target on Xenon Pharmaceuticals stock to $60 from $78 while keeping a Buy rating, removing all sales projections for major depressive disorder and bipolar disorder from its model for AZK, leaving the target to reflect only AZK's potential in epilepsy. Deutsche Bank downgraded the stock from Buy to Hold and slashed its price target from $90 to $46, citing safety concerns, while H.C. Wainwright kept its Buy rating and $74 price target, noting a pre-NDA meeting with the FDA raised no concerns about inadequate drug exposure levels. Analyst price targets now range from a low of $46 to a high of $100.
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Biotech & Genomic Medicine › Neuroscience & Neurodegenerative ▼Technology
XENE · Capital · Negative Needham cut its price target to $60 and Deutsche Bank downgraded to Hold with a $46 target, removing MDD/bipolar sales projections.
XENE · Technology · Negative Xenon paused Phase 3 enrollment for its depression/bipolar AZK trials after neuropsychiatric side effects, delaying the program.
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United StatesCanada
Biotech & Genomic Medicine2impact 4

Xenon Pauses Psychiatry Trials Enrollment Despite Positive NDA Data

Xenon Pharmaceuticals submitted a New Drug Application to the US FDA for azetukalner in focal seizures, supported by two randomized, double-blind, placebo-controlled trials showing statistically significant seizure reduction and a generally consistent safety profile across more than 1,500 patient-years of exposure. On the same day, the company voluntarily paused new enrollment in its Phase 3 major depressive disorder and bipolar depression studies due to neuropsychiatric adverse events, a precaution that could reshape expectations for azetukalner's use beyond epilepsy. The enrollment pause does not directly affect the epilepsy NDA or ongoing Phase 3 seizure studies, which remain the main driver of the investment story. Xenon's narrative projects $449.0 million revenue and $79.2 million earnings by 2029, requiring an earnings increase of $488.4 million from -$409.2 million today, while some of the lowest estimate analysts assume only US$169.5 million of revenue and US$30.0 million of earnings by 2029.
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Biotech & Genomic Medicine › Neuroscience & Neurodegenerative ▼Regulation
XENE · Regulation · Positive Xenon submitted an NDA to the FDA for azetukalner in focal seizures, supported by two positive Phase 3 trials.
XENE · Technology · Negative Xenon voluntarily paused new enrollment in its Phase 3 MDD and bipolar depression studies due to neuropsychiatric adverse events.
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United States
XENE▼

Xenon plunges 24% on trial pause; Netflix downgraded by Wells Fargo

Xenon Pharmaceuticals plunged 24% in premarket trading after submitting a New Drug Application to the U.S. Food and Drug Administration for azetukalner as a treatment for focal seizures in epilepsy while voluntarily pausing new patient enrollment in ongoing Phase 3 trials for major depressive disorder and bipolar depression. Netflix slipped 2.1% after Wells Fargo downgraded the streaming giant to Underweight from Equal Weight and cut its price target to $57 from $80, citing weakening engagement trends. Array Technologies fell 3.1% to $4.11 after UBS downgraded the solar tracking company to Neutral from Buy and cut its price target to $5 from $10, pointing to a shift from payment-in-kind to cash payments on preferred dividend obligations that UBS estimates will total roughly $162 million in cumulative cash payments through 2030. Steel Dynamics dropped 3.4% after guiding third-quarter 2026 earnings to $5.34 to $5.38 per diluted share, below the analyst consensus of $5.60. Frontline fell 6% as the tanker company went ex-dividend for a combined payout of $3.41 per share, made up of a regular second-quarter dividend of $2.61 and a special dividend of $0.80 funded by the sale of two very large crude carriers.
ARRY · Capital · Negative UBS downgraded Array Technologies to Neutral and cut its price target to $5 from $10 on preferred dividend cash-payment concerns.
FRO · Capital · Negative Frontline fell 6% as it went ex-dividend for a combined $3.41 per share payout.
NFLX · Capital · Negative Wells Fargo downgraded Netflix to Underweight and cut its price target to $57 from $80, citing weakening engagement trends.
STLD · Capital · Negative Steel Dynamics guided Q3 2026 earnings to $5.34-$5.38 per share, below the $5.60 analyst consensus.
XENE · Regulation · Negative Xenon voluntarily paused new patient enrollment in ongoing Phase 3 trials for major depressive disorder and bipolar depression while submitting its azetukalner NDA to the FDA.
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Biotech & Genomic Medicine▲

BofA downgrades Biohaven to Underperform, cuts price target to $11

BofA downgraded Biohaven to Underperform from Neutral and lowered its price target to $11 from $12, citing a cautious view of the near-term risk-reward profile ahead of pivotal Phase 3 data for the company's Kv7 epilepsy program expected in the second half of the year. The firm noted Biohaven trails a competing program from Xenon Pharmaceuticals by at least two years and believes consensus expectations for approximately $1 billion in peak sales could face downside risk unless the company demonstrates meaningful clinical differentiation. Earlier, on June 26, Deutsche Bank raised its price target on Biohaven to $20 from $15 while maintaining a Buy rating, highlighting the troriluzole program for spinocerebellar ataxia as a potentially significant value driver that could benefit from the FDA's recent willingness to reconsider previous regulatory decisions in certain neurological diseases.
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Biotech & Genomic Medicine › Neuroscience & Neurodegenerative Competition
BHVN · Capital · Negative BofA downgraded Biohaven to Underperform and cut price target to $11, citing cautious risk-reward ahead of Phase 3 data and trailing competitor.
XENE · Competition · Positive Xenon's Kv7 program is noted as at least two years ahead of Biohaven's, giving Xenon a competitive advantage.
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Biotech & Genomic Medicine▲

Xenon Pharmaceuticals Stock Gains 22% in Six Months on Azetukalner Progress

Xenon Pharmaceuticals shares have risen approximately 22% over the past six months, outperforming the industry's 5.2% decline, driven by investor confidence in its neuroscience pipeline. The lead asset azetukalner met its primary endpoint in the phase III X-TOLE2 study for focal onset seizures, with the 25 mg dose showing a placebo-adjusted median percent change in monthly seizure frequency of -42.7%. Xenon plans to submit a new drug application to the FDA in the third quarter of 2026, and if approved, azetukalner would become the only KV7 potassium channel opener for epilepsy. The company is also advancing azetukalner in phase III studies for major depressive disorder and bipolar depression, with top-line data from the X-NOVA2 MDD study expected in the first half of 2027. Early-stage assets XEN1120 and XEN1701 are in phase I trials for pain, with data anticipated in the second half of 2026.
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Biotech & Genomic Medicine › Neuroscience & Neurodegenerative Competition
XENE · Technology · Positive Azetukalner met primary endpoint in phase III study for focal onset seizures, with NDA submission planned.
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