Why Did PRAX Stock Rocket 24% Pre-Market Today?

The Data Monitoring Committee (DMC) recommended stopping the EMBOLD study ahead of schedule after the interim analysis demonstrated strong positive outcomes.
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Rising stock market chart on a trading board background. | Image source: Yuichiro Chino on Getty Images
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Shivani Kumaresan·Stocktwits
Published Dec 05, 2025   |   6:10 AM EST
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  • Relutrigine targets patients suffering from severe, genetic epilepsy syndromes.
  • To date, no approved therapy specifically addresses these conditions, making the trial’s success potentially important.
  • Praxis will present the topline EMBOLD results on December 6 at the American Epilepsy Society’s meeting.

Praxis Precision Medicines, Inc. (PRAX) stock is on track to reach its January 2022 highs on Friday, after its experimental epilepsy drug candidate, relutrigine, produced positive results in the trials. 

The Data Monitoring Committee (DMC) recommended stopping the study ahead of schedule after an interim analysis demonstrated strong positive outcomes. 

Praxis Precision’s stock traded over 24% higher in Friday’s premarket. On Stocktwits, retail sentiment around the stock improved to ‘extremely bullish’ from ‘bullish’ territory the previous day. Message volume jumped to ‘extremely high’ from ‘normal’ levels in 24 hours. 

PRAX’s Sentiment Meter and Message Volume as of 05:30 a.m. ET on Dec. 5, 2025 | Source: Stocktwits
PRAX’s Sentiment Meter and Message Volume as of 05:30 a.m. ET on Dec. 5, 2025 | Source: Stocktwits

Why This Matters

Relutrigine targets patients suffering from severe, genetic epilepsy syndromes and developmental and epileptic encephalopathies (DEEs), neurological disorders marked by frequent seizures and high mortality. 

To date, no approved therapy specifically addresses these conditions, making the trial’s success potentially important for affected children and families worldwide. 

What Comes Next

Following the DMC’s recommendation, Praxis will present the topline EMBOLD results on December 6 at the American Epilepsy Society’s meeting in Atlanta. If regulatory discussions with the FDA go favorably, the company could soon file a New Drug Application (NDA) for relutrigine.

Basically, Relutrigine works as a preferential inhibitor of persistent sodium current, shown to be a key driver of seizure symptoms in severe DEEs. 

Studies in live animal models show that relutrigine can reduce seizures in a dose-dependent way, even stopping them entirely in mice with SCN2A, SCN8A, and other DEE conditions. The drug has also been well-tolerated in three Phase 1 trials. 

PRAX stock has gained over 146% in 2025 and over 178% in the last 12 months. 

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