Pulling SEC filings + quote and writing the call…

Anteris Technologies Global Corp.
Next earnings Aug 10, 2026 · consensus $-0.21 EPS, $1.51M rev
Last earnings -2.5% on 2026-05-13
Clinical-stage cash burner trading at 522x sales with negative equity — investable only as a binary bet on DurAVR, not a stock.
Revenue $1.91M · FY2025
Anteris is a pre-revenue structural heart company whose FY2025 financials read like a clinical-stage biotech, not an operating business: $1.91M of revenue (down 29.2% YoY) against a $94.1M net loss and $77.8M of operating cash burn. R&D alone ($69.1M) is ~36x revenue, and the accumulated deficit has reached $370.5M. Stockholders' equity has collapsed to essentially zero (-$93K, down from a positive base a year ago), and total assets fell 71.5% to $23.0M while liabilities grew 29%. By any conventional fundamentals lens this is a melting ice cube — the operating margin is -4,908% and the company explicitly warns it 'expect[s] to continue to incur additional losses for the foreseeable future.'
The entire investment case rests on a single asset: the DurAVR THV System, a biomimetic balloon-expandable aortic valve. The MD&A confirms only ~130 patients have been implanted to date, with the pivotal PARADIGM Trial just initiated — first European approval came in October 2025 (Denmark), and the FDA granted IDE approval in November 2025 for a staged enrollment of the first 200 patients. Commercial approval is years away, and the Risk Factors are blunt: 'It is possible that none of our products will be successfully commercialized.'
AI-generated analysis, produced by our proprietary engine from SEC filing data.
Investment recommendation produced by TENK/calls (tenkcalls.com), Luxembourg. Completed Jun 25, 2026, 10:23 AM ET. Ratings & methodology: definitions · All recommendations to date: track record · Conflicts: disclosures. Not investment advice.
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| Line item | FY24 | FY25 |
|---|---|---|
| Revenue | $2.70M | $1.91M |
| Gross profit | — | — |
| Operating income | -$78.4M | -$93.9M |
| Net income | -$76.3M | -$94.1M |
| Diluted EPS | -$3.68 | -$2.55 |
| Net margin | -2822.5% | -4921.3% |
Annual figures from SEC 10-K XBRL filings. Open the filing links below for full statement detail.
Computed from SEC XBRL annual figures + the current quote. EV and ROIC use long-term + current debt where filed; estimates, not investment advice.
Entered new material agreement with exhibits filed; terms expand commercial relationships.
Q1 2026 results press release furnished alongside the 10-Q; losses continue as expected.
Q1 2026 results press release furnished alongside the 10-Q; losses continue as expected.
Q1 2026 10-Q: cash bolstered by Jan $320M raise; opex and trial spend keep rising.
Termination of a material definitive agreement disclosed; removes a prior commercial tie.
Entered into a new material definitive agreement supporting PARADIGM Trial execution.
Officer/director change with exhibits; another leadership move ahead of trial scale-up.
FY25 loss widened to $94M but $320M Jan raise + Medtronic PIPE fund PARADIGM Trial.
Shelf registration filed enabling future at-will equity raises; dilution overhang risk.
Sources: SEC EDGAR (CIK 0002011514, latest 10-Q filed 2026-05-12) · EODHD · Proprietary analysis · as of 6/25/2026, 2:23:14 PM.
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Dates from 8-K (Item 2.02); beat/miss = reported EPS vs consensus (Finnhub, recent quarters); move = prior close → close on/after.
1195 tracked peers · median
Recent news tone vs the market's typical (which skews positive). A soft signal, not a recommendation.