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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
$8.3B
-
-$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 gives Praxis a near-term route into essential tremor, a large underserved market: its Phase 3 programme was positive, and the FDA’s review had raised no major safety or efficacy concerns by August. The agency was not planning an advisory committee meeting, with a decision due by January 2027. (GlobeNewswire)
Relutrigine could address severe SCN2A- and SCN8A-related epilepsies with no approved treatment for those genetic forms. In the registrational study, it delivered a 53% placebo-adjusted reduction in motor seizures, giving the application meaningful clinical support despite the extended FDA review. (NeurologyLive)
Praxis has further upside beyond its two pending drug applications: elsunersen received FDA Breakthrough Therapy designation after positive early trial results in SCN2A-related epilepsy. That offers another potential development path if later studies confirm the early findings. (GlobeNewswire)
The FDA extended relutrigine’s review by three months after treating additional analyses of existing clinical data as a major amendment. No new studies or safety concerns were cited, but the delay leaves the application exposed to further regulatory uncertainty. (GlobeNewswire)
Vormatrigine failed to meet POWER1’s primary endpoint for reducing focal seizures, and Praxis paused enrolment in a second study while reassessing the programme. This weakens the value of a pipeline asset that had been expected to broaden the company’s epilepsy opportunity. (Endpoints News)
Praxis is still pre-commercial and reported a $176.3 million net loss for the first half of 2026 as it expanded research and launch spending. A delay to approvals or slower uptake would leave it consuming cash before product sales can help fund the business. (StockTitan)
Data summarised monthly by Lightyear AI. Last updated on 3 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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