Cambridge biotech tracker · Cambridge

Parabilis Medicines

Listed on Nasdaq as PBLS, 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
$1.12B
Q2 '26 · Jun 30, 2026
Burn per quarter
$47.3M
net loss less stock comp
Runway
5+ yrs
3+ years
Net loss
$52.5M
Q2 '26
R&D expense
$39.4M
77% of opex
Raised, last 4 qtrs
$0
net financing cash flow
Next readout
Apr 2027
Phase 1/2 · cash past the catalyst

Cash & investments

Quarter-end balance

Cash & investments$0$1B$2BQ4 '24Q1 '25Q2 '25Q4 '25Q1 '26Q2 '26$1.12B
Operating cash flow

Not reported in a standard XBRL tag for this company.

R&D expense

Per quarter

R&D expense$0$25M$50MQ4 '24Q1 '25Q2 '25Q4 '25Q1 '26Q2 '26$39.4M

Two views of the runway

Compare across the cluster

The outside view

5+ years

Cash at Q2 '26 divided by the average burn of the last four quarters, $15.8M a month.

Management’s own date

Into 2030

Jan–Dec 2030

That implies $20.7M to $26.6M a month, 1.3–1.7× the recent pace.

Planning to spend faster
“We believe that our existing cash, cash equivalents and marketable securities will enable us to fund our operating expenses and capital expenditure requirements into 2030.”
10-Q for the period ended Jun 30, 2026, filed Aug 13, 2026. Open the filing

Cash against the calendar

What the runway has to reach.

Next expected readoutPhase 1/2

Apr 2027estimated

FOG-001 in Locally Advanced or Metastatic Solid Tumors

Cancer · Colorectal Cancer · Solid Tumor

NCT05919264 on ClinicalTrials.gov

Does the cash reach it?

Cash past the catalyst

Runway
5+ years
Time to the date
5 months

It is about 5 months out. At the current burn there is roughly 66 months of cash left on the far side of it, which is enough room to raise on the result rather than ahead of it.

Pipeline

1 active trial, through phase 1/2.

Phase 1/2 · 1

Study
FOG-001 in Locally Advanced or Metastatic Solid TumorsNCT05919264 · Cancer, Colorectal CancerPhase 1/2Apr 2027est.

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 phase 1/2 readout in Apr 2027, about 5 months out. That leaves roughly 66 months of cash afterwards, which is the position you want: the raise can be negotiated on the data instead of on the calendar.

About 5+ years of runway

Cash and investments of $1.12B at Q2 '26 against an average operating cash burn of $47.3M per quarter over the last four reported quarters runs out around May 2032. More than two years of runway means the finance conversation is about deployment, not survival.

Cash position up $1.07B since Q4 '24

No meaningful financing inflows over the last four quarters, so the change is essentially operating burn. The balance is the number the board watches; the trend is the number the auditors watch.

R&D is 77% of operating expenses

$39.4M of R&D against $51.0M of total operating expenses in Q2 '26, with G&A at $11.7M. 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.

Revenue of $148K in Q2 '26

The balance sheet carries $41.5M of deferred revenue, which is typically upfront collaboration or license payments being recognized over time. Collaboration and license revenue under ASC 606 and ASC 808 is the single most judgment-heavy area in biotech accounting: performance obligations, variable consideration on milestones, and the split between revenue and cost-sharing.

Accumulated deficit of $639M

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
Q4 '24 · Dec 31, 24$50.1M———————
Q1 '25 · Mar 31, 25——−$38.3M—————
Q2 '25 · Jun 30, 25$80.4M—−$34.8M$30.1M$6.4M$0$823K—
Q4 '25 · Dec 31, 25$27.7M———————
Q1 '26 · Mar 31, 26——−$45.3M—————
Q2 '26 · Jun 30, 26$1.12B—−$52.5M$39.4M$11.7M$148K$3.6M—

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.