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Praxis Precision Medicines/$PRAX

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About Praxis Precision Medicines

Praxis Precision Medicines Inc is a clinical-stage biopharmaceutical company. It is engaged in translating genetic insights into the development of therapies for patients affected by central nervous system disorders characterized by a neuronal excitation-inhibition imbalance. The company applies genetic insights to the discovery and development of therapies for neurological disorders through two proprietary platforms: Cerebrum and Solidus. It has established a diversified, multimodal CNS portfolio with four clinical-stage product candidates across movement disorders and epilepsy, which include Ulixacaltamide, Relutrigine, Vormatrigine, and Elsunersen. The firm operates in only one segment and is focused on discovering and developing therapies for CNS disorders.
Ticker
$PRAX
Sector
Health
Primary listing
NASDAQ
Employees
168

PRAX Metrics

BasicAdvanced
$8B
-
-$12.86
2.78
-

What the Analysts think about PRAX

Analyst ratings (Buy, Hold, Sell) for Praxis Precision Medicines stock.
Analyst projections of the future price of Praxis Precision Medicines stock.

Bulls say / Bears say

Ulixacaltamide could give Praxis a first-mover opportunity in essential tremor: it is the first investigational treatment to report positive Phase 3 results for a condition affecting about seven million people in the US. The FDA’s mid-cycle review found no major safety or efficacy concerns, and no advisory committee meeting is planned. (Praxis Precision Medicines)
Relutrigine offers a second near-term approval catalyst in rare genetic epilepsy and, if approved, could be the first treatment for SCN2A and SCN8A developmental and epileptic encephalopathies. Its FDA review found no major safety or efficacy concerns, with a decision due by 27 December 2026. (Praxis Precision Medicines)
Elsunersen adds longer-term pipeline potential: positive results from its early study led to the FDA granting Breakthrough Therapy Designation. Its registrational EMBRAVE3 study is enrolling, with results expected in 2027. (Praxis Precision Medicines)
Vormatrigine failed to meet the primary endpoint in the POWER1 focal-seizure study, and Praxis paused enrolment in another trial while it reassessed the programme. That leaves the drug’s development path and commercial potential less certain. (Reuters)
The FDA classified additional sensitivity analyses for relutrigine as a major amendment, pushing its decision date back three months to 27 December 2026. The delay creates further uncertainty for a key near-term approval catalyst. (Praxis Precision Medicines)
Praxis is still making substantial losses as it builds towards commercial launches: its second-quarter net loss widened to $83.7 million from $71.1 million a year earlier, while general and administrative expenses more than doubled. The company has sizeable cash reserves, but it must turn that rising spend into approved products and sales. (Praxis Precision Medicines)
Data summarised monthly by Lightyear AI. Last updated on 19 Oct 2026.

PRAX Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

PRAX Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
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