| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 7.46M | 8.55M | 2.45M | 0.00 | 0.00 | 0.00 |
| Gross Profit | 7.37M | 8.55M | 2.45M | -1.17M | -1.59M | -746.00K |
| EBITDA | -288.03M | -199.81M | -125.94M | -212.86M | -165.47M | -61.08M |
| Net Income | -273.04M | -182.82M | -123.28M | -213.07M | -166.88M | -61.82M |
Balance Sheet | ||||||
| Total Assets | 396.39M | 483.11M | 87.95M | 115.13M | 292.75M | 303.18M |
| Cash, Cash Equivalents and Short-Term Investments | 267.16M | 392.57M | 81.30M | 100.49M | 275.91M | 296.61M |
| Total Debt | 436.00K | 1.37M | 2.50M | 4.50M | 4.31M | 763.00K |
| Total Liabilities | 52.88M | 37.66M | 18.28M | 39.02M | 41.94M | 15.72M |
| Stockholders Equity | 343.50M | 445.45M | 69.67M | 76.11M | 250.81M | 287.46M |
Cash Flow | ||||||
| Free Cash Flow | -228.92M | -131.76M | -111.19M | -185.49M | -125.60M | -52.62M |
| Operating Cash Flow | -228.87M | -131.76M | -111.14M | -185.04M | -124.55M | -52.62M |
| Investing Cash Flow | 6.33M | -248.49M | 38.95M | 96.89M | -140.52M | 4.00K |
| Financing Cash Flow | 203.42M | 514.32M | 91.87M | 10.46M | 107.59M | 304.42M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
58 Neutral | $4.15B | ― | -60.98% | ― | 338.45% | -19.64% | |
56 Neutral | $1.35B | -12.21 | ― | ― | ― | ― | |
55 Neutral | $1.26B | ― | -88.40% | ― | ― | ― | |
52 Neutral | $860.78M | ― | -23.56% | ― | 22367.80% | -5.15% | |
52 Neutral | $867.63M | ― | -32.78% | ― | -13.37% | -1025.90% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
49 Neutral | $1.46B | ― | -15.64% | ― | -0.54% | -6.28% |
Praxis Precision Medicines, Inc. is conducting a clinical trial titled ‘A Randomized, Multi-Center, Double-Blind, Sham-Procedure-Controlled Clinical Trial to Investigate the Efficacy and Safety of Elsunersen in Pediatric Participants With Early Onset SCN2A Developmental and Epileptic Encephalopathy.’ The study aims to evaluate the efficacy and safety of Elsunersen in treating pediatric patients with SCN2A-related epileptic encephalopathy, a severe neurological disorder.
Praxis Precision Medicines, Inc. is conducting a Phase 3 clinical trial titled A Clinical Trial for Participants With DEE to Assess Efficacy, Safety, Tolerability, and PK of Relutrigine. The study aims to evaluate the effectiveness and safety of Relutrigine in treating Developmental and Epileptic Encephalopathies (DEE), a severe neurological condition. This trial is significant as it seeks to provide a new therapeutic option for individuals affected by DEE.
Praxis Precision Medicines, Inc. is conducting a Phase 3 clinical study titled ‘Essential 3,’ which aims to evaluate the safety and efficacy of ulixacaltamide in treating essential tremor. This study is significant as it seeks to determine whether ulixacaltamide can be a safe and effective treatment option for patients suffering from this condition.
Praxis Precision Medicines, Inc. is conducting a clinical trial titled ‘A Seamless, Clinical Trial to Investigate the Safety and Efficacy of Multiple Doses of PRAX-222 in Pediatric Participants With Early Onset SCN2A Developmental and Epileptic Encephalopathy.’ The study aims to assess the safety and efficacy of PRAX-222 in children aged 2 to 18 years with this rare neurological condition, which could significantly impact treatment options for affected families.
Praxis Precision Medicines, Inc. is conducting a clinical study titled ‘A Double-Blind, Randomized, Multicenter, Trial Evaluating the Efficacy and Safety of PRAX-628 in Adults With Focal Seizures (POWER1)’. The study aims to assess the effectiveness and safety of PRAX-628 in treating adults with focal seizures, a condition characterized by localized brain activity leading to seizures. This research is significant as it could offer a new therapeutic option for patients with limited treatment choices.
Praxis Precision Medicines, Inc. is conducting an open-label clinical trial titled ‘An Open Label Clinical Trial to Evaluate the Efficacy and Safety of PRAX-628 in Adult Patients With Focal Onset or Primary Generalized Tonic-Clonic Seizures.’ The study aims to assess the efficacy and safety of PRAX-628, a drug intended to treat focal onset and tonic-clonic seizures in adults. This research is significant as it could lead to a new treatment option for epilepsy patients.
Praxis Precision Medicines, Inc. (PRAX) is conducting a Phase 1 clinical trial titled ‘A Phase 1, Randomized, Open-Label, 2-Way Crossover Clinical Trial in Healthy Participants to Evaluate the Relative Bioavailability of PRAX-628 Tablet Formulation Compared to Capsule Formulation.’ The study aims to assess the bioavailability of PRAX-628 when administered as a tablet versus a capsule, which is crucial for determining the most effective delivery method for this drug.
Praxis Precision Medicines, Inc. is conducting a Phase 2 clinical trial titled ‘A Clinical Trial of PRAX-562 in Subjects With Developmental and Epileptic Encephalopathies (DEE).’ The study aims to assess the safety, tolerability, efficacy, and pharmacokinetics of PRAX-562 in pediatric patients with SCN2A and SCN8A encephalopathies, conditions characterized by early-onset seizures.
On October 21, 2025, Praxis Precision Medicines updated its corporate presentation for investors and analysts, highlighting its recent progress and future plans. The company announced that the FDA granted a Type B meeting for its drug candidate ulixacaltamide, following the review of the Essential3 topline results, indicating a significant step forward in its regulatory process for treating essential tremor.
The most recent analyst rating on (PRAX) stock is a Hold with a $181.00 price target. To see the full list of analyst forecasts on Praxis Precision Medicines stock, see the PRAX Stock Forecast page.
On October 16, 2025, Praxis Precision Medicines announced positive topline results from its Phase 3 Essential3 program for ulixacaltamide, aimed at treating essential tremor. The studies demonstrated statistically significant improvements in patients’ conditions, with ulixacaltamide showing a 4.3-point mean improvement in mADL11 scores compared to placebo. The drug was generally well tolerated, with no drug-related serious adverse events reported. These results position Praxis favorably within the neurological treatment market and potentially offer a new therapeutic option for essential tremor, pending regulatory approval.
The most recent analyst rating on (PRAX) stock is a Buy with a $270.00 price target. To see the full list of analyst forecasts on Praxis Precision Medicines stock, see the PRAX Stock Forecast page.
Praxis Precision Medicines, Inc. announced the termination of its 2024 Sales Agreement with Jefferies LLC on September 2, 2025, which previously allowed the company to sell shares of its common stock up to $250 million. This decision halts further sales under the 2024 ATM Program after raising approximately $86.2 million. Subsequently, on September 5, 2025, Praxis entered into a new sales agreement with TD Securities (USA) LLC to offer shares worth up to $250 million through an ‘at the market’ equity offering program, indicating a strategic shift in its capital-raising approach.
The most recent analyst rating on (PRAX) stock is a Buy with a $117.00 price target. To see the full list of analyst forecasts on Praxis Precision Medicines stock, see the PRAX Stock Forecast page.
Praxis Precision Medicines, Inc. recently held an earnings call that was predominantly positive, highlighting significant achievements in their clinical trials. The company expressed optimism regarding the efficacy of their treatments, particularly vormatrigine, which demonstrated best-in-disease results. However, challenges such as a high discontinuation rate in the RADIANT study were also acknowledged.
Praxis Precision Medicines, Inc. is a clinical-stage biopharmaceutical company focused on developing therapies for central nervous system disorders characterized by neuronal excitation-inhibition imbalance, utilizing genetic insights to address both rare and common neurological disorders.