Compare

Praxis Precision Medicines/$PRAX

1D1W1M3M6MYTD1Y5YMAX

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
$9.1B
-
-$12.76
2.84
-

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 has delivered positive Phase 3 results in essential tremor, and its NDA is under FDA review with a January 2027 decision date. Praxis is already building its sales team, giving it a route to launch quickly if approved. (GlobeNewswire)
Relutrigine showed a 53% placebo-adjusted reduction in seizures at week 16 in its confirmatory trial cohort. If approved, it could be the first treatment for SCN2A and SCN8A developmental epilepsies, where treatment options are limited. (Fierce Biotech, GlobeNewswire)
Praxis had $1.3 billion in cash and investments at the end of September, which management expects to fund operations into 2028. That gives it room to prepare potential launches and advance its pipeline without an immediate need to raise more capital. (GlobeNewswire)
The FDA extended relutrigine’s review by three months after classifying added sensitivity analyses as a major amendment, moving its decision date to 27 December 2026. The extra review time adds uncertainty around a key near-term catalyst. (Praxis Precision Medicines)
Vormatrigine missed the main endpoint in the POWER1 trial, and Praxis paused enrolment in POWER2 while it reassessed the programme. This setback weakens the breadth of the pipeline and leaves the drug’s future benefit less certain. (Reuters)
Commercial preparation is becoming costly: third-quarter general and administrative expenses rose to $42.7 million from $12.6 million a year earlier, while the net loss widened to $94.2 million. Higher spending makes delays or a slow launch more costly to absorb. (GlobeNewswire)
Data summarised monthly by Lightyear AI. Last updated on 9 Nov 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
Data displayed above is indicative only and its accuracy or completeness is not guaranteed. Actual execution price may vary. Past performance is not indicative of future results. Your return may be affected by currency fluctuations and applicable fees and charges. Capital at risk.
Real-time US market data is sourced from the IEX order book provided by Polygon. After-hours US market data is 15 minutes delayed and may differ significantly from the actual tradable price at market open.