Cambridge biotech tracker · Boston

Praxis Precision Medicines

Listed on Nasdaq as PRAX, filed under SEC industry code 2834 (pharmaceutical preparations). Fiscal year ends in December. Numbers below are from the company’s own SEC filings through Q2 '26.

Cash & investments
$1.37B
Q2 '26 · Jun 30, 2026
Burn per quarter
$76.3M
avg. operating cash flow, 4 qtrs
Runway
4.5 yrs
3+ years
Net loss
$83.7M
Q2 '26
R&D expense
$69.4M
72% of opex
Raised, last 4 qtrs
+$1.23B
net financing cash flow
FDA decision
Jan 2027
FDA decision · cash past the catalyst

Cash & investments

Quarter-end balance

Cash & investments$0$1B$2BQ3 '24Q4 '24Q1 '25Q2 '25Q3 '25Q4 '25Q1 '26Q2 '26$1.37B$1.45B

Operating cash flow

Per quarter; below zero is burn

Operating cash flow−$100M−$50M$0Q3 '24Q4 '24Q1 '25Q2 '25Q3 '25Q4 '25Q1 '26Q2 '26−$77.5M−$86.2M

R&D expense

Per quarter

R&D expense$0$50M$100MQ3 '24Q4 '24Q1 '25Q2 '25Q3 '25Q4 '25Q1 '26Q2 '26$69.4M$78.0M

Two views of the runway

Compare across the cluster

The outside view

4.5 years

Cash at Q2 '26 divided by the average burn of the last four quarters, $25.4M a month.

Management’s own date

Into 2028

Jan–Dec 2028

That implies $45.7M to $76.0M a month, 1.8–3.0× the recent pace.

Planning to spend faster
“We expect that our cash, cash equivalents, and marketable securities as of June 30, 2026 will be sufficient to fund our operating expenditures and capital expenditure requirements necessary to advance our operating activities into 2028.”
10-Q for the period ended Jun 30, 2026, filed Aug 6, 2026. Open the filing

Cash against the calendar

What the runway has to reach.

Next FDA decisionFDA decision

Jan 29, 2027

FDA target action date (PDUFA)

Disclosed in the 8-K filed Aug 6, 2026

Does the cash reach it?

Cash past the catalyst

Runway
4.5 years
Time to the date
3 months

It is about 3 months out. At the current burn there is roughly 51 months of cash left on the far side of it, which is enough room to raise on the result rather than ahead of it.

FDA decision dates disclosed in filings

  • Dec 27, 2026PDUFA target action date8-K filed Aug 6, 2026

    “…-cycle meeting completed for relutrigine FDA identified no major safety or efficacy concerns to date and does not plan to request an advisory committee meeting PDUFA date of December 27, 2026 FDA Bioresearch Monitoring (BIMO) inspections of Praxis for both ulixacaltamide and relutrigine completed with no Form FDA 483 observations Commerci…”

  • Jan 29, 2027PDUFA target action date8-K filed Aug 6, 2026

    “…meeting completed for ulixacaltamide HCl FDA identified no major safety or efficacy concerns to date and does not plan to request an advisory committee meeting PDUFA date of January 29, 2027 Mid-cycle meeting completed for relutrigine FDA identified no major safety or efficacy concerns to date and does not plan to request an advisory comm…”

Pulled from the company’s own filing text. An approval decision is a financing event as much as a clinical one, since the commercial build-out has to be funded months before any revenue from it arrives.

Pipeline

8 active trials, through phase 3.

Phase 3 · 5Phase 2/3 · 1Phase 1/2 · 1Phase 2 · 1

Study
Essential 3 - Decentralized, Phase 3 Study Evaluating the Safety and Efficacy of Ulixacaltamide in Essential Tremor (ET)NCT06087276 · Essential TremorPhase 3Oct 2025
A Clinical Trial of Elsunersen in Pediatric SCN2A-DEE to Assess Efficacy and SafetyNCT07019922 · Epileptic Encephalopathy, SCN2A EncephalopathyPhase 3Dec 2026est.
A Clinical Trial for Participants With DEE to Assess Efficacy, Safety, Tolerability, and PK of RelutrigineNCT07010471 · Developmental and Epileptic Encephalopathy 1Phase 3Dec 2026est.
Randomized Clinical Trial Evaluating the Efficacy and Safety of Vormatrigine in Adults With Focal SeizuresNCT07505004 · Focal EpilepsyPhase 3Jan 2027est.
Clinical Trial of Vormatrigine in Adult Patients With EpilepsyNCT07287163 · Epilepsy, Tonic-Clonic, Focal SeizurePhase 3May 2028est.
A Clinical Trial of PRAX-562 in Subjects With Developmental and Epileptic Encephalopathies (DEE)NCT05818553 · SCN2A Encephalopathy, SCN8A EncephalopathyPhase 2/3Nov 2025
An Open Label Trial to Evaluate the Efficacy and Safety of PRAX-628 in Adults With Focal Onset or Tonic-Clonic SeizuresNCT06908356 · Focal Onset Seizure, Primary Generalized EpilepsyPhase 2Jul 2025est.· not a catalyst
A Clinical Trial of PRAX-222 in Pediatric Participants With Early Onset SCN2A Developmental and Epileptic EncephalopathyNCT05737784 · SCN2A-DEE, EpilepsyPhase 1/2Apr 2026
Double-blind, Randomized Trial of PRAX-628 in Adults With Focal Seizures to Evaluate Efficacy and Safety (POWER1)NCT06999902 · Focal SeizurePhase 2/3May 2026
A Clinical Trial to Evaluate the Relative Bioavailability of PRAX-628NCT06840925 · HealthyPhase 1Jun 2025

Interventional studies where this company is the lead sponsor, from ClinicalTrials.gov. Primary completion is when the last patient is measured on the primary endpoint, which is when the data exists rather than when it is announced. Extension, rollover and healthy-volunteer studies are listed but marked as non-catalysts, because they finish long after the result that mattered. Sponsors revise these dates as enrollment moves, so an estimate is a plan rather than a promise.

The controller’s read

What the filings say.

Generated from the numbers above using the same questions I ask when I open a client’s books: how long the cash lasts, what is driving the gap between loss and burn, and where the accounting judgment sits.

Get this read on your company

The cash clears the next catalyst

The next dated event is a FDA target action date in Jan 2027, about 3 months out. That leaves roughly 51 months of cash afterwards, which is the position you want: the raise can be negotiated on the data instead of on the calendar.

About 4.5 years of runway

Cash and investments of $1.37B at Q2 '26 against an average operating cash burn of $76.3M per quarter over the last four reported quarters runs out around December 2030. More than two years of runway means the finance conversation is about deployment, not survival.

Cash position up $963M since Q3 '24

Net financing inflows of $1.23B over the last four quarters, from equity, debt, or ATM sales, more than covered operating burn. The balance is the number the board watches; the trend is the number the auditors watch.

R&D is 72% of operating expenses

$69.4M of R&D against $96.9M of total operating expenses in Q2 '26, with G&A at $27.5M. For a clinical-stage company, the accounting questions live inside that R&D line: CRO and CMC accruals, milestone recognition, and what gets capitalized versus expensed under ASC 730.

Accumulated deficit of $1.32B

Total losses since inception. It is also roughly the size of the net operating loss carryforward the tax provision has to track, subject to Section 382 limits after each ownership change.

Quarterly detail, eight quarters
QuarterCash & inv.Op. cash flowNet incomeR&DG&ARevenueStock compFinancing
Q3 '24 · Sep 30, 24$411M−$27.5M−$51.9M$41.9M$15.3M$302K$12.4M$1.4M
Q4 '24 · Dec 31, 24$215M−$56.1M−$58.7M$56.3M$15.1M$7.5M$8.6M$114M
Q1 '25 · Mar 31, 25$472M−$53.0M−$69.3M$60.8M$13.9M$0$8.8M$54.3M
Q2 '25 · Jun 30, 25$447M−$54.7M−$71.1M$63.0M$13.1M$0$7.8M$28.6M
Q3 '25 · Sep 30, 25$389M−$65.1M−$73.9M$65.8M$12.6M$0$7.4M$6.8M
Q4 '25 · Dec 31, 25$926M−$76.3M−$88.6M$77.5M$19.5M$0$9.9M$613M
Q1 '26 · Mar 31, 26$1.45B−$86.2M−$92.6M$78.0M$27.9M—$17.1M$609M
Q2 '26 · Jun 30, 26$1.37B−$77.5M−$83.7M$69.4M$27.5M—$11.3M$4.6M

Source: SEC EDGAR XBRL company facts, latest filed value for each period. Fourth quarters are derived from annual less nine-month figures; quarterly cash flows are derived from year-to-date amounts. Not investment advice. If a figure disagrees with the filing, the filing is right.