Nanobiotix Q2FY27 Results: Net loss widens to €34.3m on revenue drop
- Net loss widened to €34.3 million in H1 2026 from €5.4 million in H1 2025
- Revenue and other income dropped to €5.6 million from €26.6 million year-on-year
- Cash position strengthened to €110.9 million as of June 30, 2026
- R&D expenses decreased slightly to €12.7 million from €14.5 million
- Lead candidate JNJ-1900 showed 79% locoregional control in Phase 1 NSCLC study

*this image is generated using AI for illustrative purposes only.
Nanobiotix (NASDAQ: NBTX) reported a net loss of €34.3 million for the first half of 2026, a significant expansion from the €5.4 million loss recorded in the same period of 2025. The widened deficit stems primarily from a steep decline in revenue and other income, which fell to €5.6 million from €26.6 million year-on-year.
The variance is largely attributable to a one-off non-cash revenue impact of €21.2 million recognized in H1 2025 following the transfer of NANORAY-312 study sponsorship to Johnson & Johnson. Excluding this accounting adjustment, operational expenses remained relatively stable, with R&D spending decreasing slightly to €12.7 million from €14.5 million.
Financial performance overview
The company’s cash position strengthened significantly during the period, aided by a successful capital raise. Cash and cash equivalents stood at €110.9 million as of June 30, 2026, compared to €52.8 million at the end of 2025. This increase supports management’s guidance that current funds will extend the cash runway into 2029.
| Metric | H1 2026 | H1 2025 | Change |
|---|---|---|---|
| Revenue and other income | €5.6 million | €26.6 million | -€21.0 million |
| R&D expenses | €12.7 million | €14.5 million | -€1.8 million |
| SG&A expenses | €10.8 million | €11.3 million | -€0.5 million |
| Net loss | €34.3 million | €5.4 million | +€28.9 million |
| Cash and equivalents | €110.9 million | N/A | +€58.1 million (vs Dec 2025) |
Operational highlights
Nanobiotix advanced its clinical pipeline through several key milestones involving its lead candidate, JNJ-1900 (NBTXR3):
- Phase 1 NSCLC Study: Data presented at the 2026 WCLC Meeting showed a one-year locoregional control rate of 79% and overall survival of 70% in evaluable patients. No dose-limiting toxicities were reported among the 24 patients treated.
- Phase 2 CONVERGE Study: Early results from the Johnson & Johnson-led study in unresectable Stage 3 NSCLC indicated an overall response rate of 85.7% and a complete response rate of 57.1% in seven patients.
- Phase 3 NANORAY-312: The FDA cleared a protocol amendment that eliminates the interim analysis and modifies the final analysis to include fewer events, aiming for earlier completion.
- Capital Raise: The company completed an oversubscribed global follow-on offering in May 2026, generating approximately €86 million in gross proceeds.
What the numbers show
A critical divergence exists between the reported net loss and the underlying operational burn. While the net loss expanded by €28.9 million, this figure is heavily skewed by the absence of the €21.2 million non-cash revenue recognition from the prior year. When isolating operational costs, R&D expenses fell by €1.8 million and SG&A decreased by €0.5 million, indicating that core spending discipline was maintained despite the headline loss increase. The primary driver of the financial deterioration was the structural change in revenue recognition tied to the J&J partnership, rather than an escalation in cash outflows.
Strategic positioning
Laurent Levy, Chief Executive Officer and Chairman, stated that the company remains strategically equipped to support the development of Nanoradioenhancer JNJ-1900 (NBTXR3) and next-generation platforms like Nanoprimer. The inclusion of Nanobiotix in the Euronext Tech Leaders Index further underscores its standing among high-growth European technology firms.
How will the FDA-approved protocol amendment for the Phase 3 NANORAY-312 trial specifically alter the projected timeline for final data readout and potential regulatory submission?
Given the 85.7% overall response rate in early CONVERGE data, what are the specific criteria Johnson & Johnson must meet before triggering milestone payments to Nanobiotix?
With cash reserves extending into 2029, does Nanobiotix plan to initiate new clinical trials for its next-generation Nanoprimer platform, or remain focused solely on JNJ-1900?






























