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News articleYahoo Finance· June 2, 2026

Nanobiotix Provides First Quarter 2026 Operational and Financial Update

View original at finance.yahoo.com
Nanobiotix Provides First Quarter 2026 Operational and Financial Update Nanobiotix S.A…
Opening lines of the source · Yahoo Finance · short snapshot — read the full document at the original

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  • Complete response rate of 57.1% (4/7 patients) observed in CONVERGE Part 1 cohort, reported at ESTRO 2026

    60% confidence
  • With standard of care (cCRT ± durvalumab), depth of response in Stage 3 Inoperable NSCLC is limited with very low rates of complete response below 5%

    60% confidence
  • Nanoprimer pre-treatment followed by LNP-DNA administration showed increased systemic bioavailability, reduced hepatic toxicity, and reduced cGAS-STING related inflammation compared to LNP-DNA alone in preclinical data

    60% confidence
  • Absence of progressive disease and deepening response over time in CONVERGE patients suggests potential for long-term durability of JNJ-1900 treatment

    60% confidence
  • ORR of 71.4% (5/7 patients) observed at earlier time point in same CONVERGE cohort and reported at ELCC 2026

    60% confidence
  • Early results suggest intratumoral/intranodal injection of JNJ-1900 is feasible and can be performed safely in patients with stage III unresectable NSCLC

    60% confidence
  • Overall response rate of 85.7% (6/7 patients) observed in CONVERGE Part 1 cohort following full treatment regimen of cCRT, JNJ-1900, and durvalumab consolidation, reported at ESTRO 2026

    60% confidence
  • CONVERGE treatment procedure demonstrated an acceptable safety profile without serious treatment-emergent adverse events

    60% confidence
  • Nanobiotix continues to advance with focus, discipline, and ambition to unlock the full potential of physics-based nanotherapeutics; Q1 2026 strengthened the foundation via JNJ-1900 advancement, Nanoprimer progress, and reinforced financial position

    60% confidence

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What we know · the intelligence behind this page
Live from the substrate
What we're seeing
Q4 2026 Clinical Catalyst Season: Big-Pharma Data Flow, Regulatory Milestones, and a Thin AI-Drug Fringe
October 2026 conferences (EASD, IGCS, NACFC, HFSA) are producing a dense run of late-stage readouts from Novo Nordisk, Lilly, Roche, Bayer, Vertex and Galderma. Regulatory milestones are scheduled behind them: the ivonescimab BLA PDUFA date on 2026-11-14, FDA acceptance of Roche's vamikibart BLA, and Scholar Rock's EMA resubmission. The AI-and-finance angle is peripheral. It consists of the AI-designed drug Rentosertib and QAIAx, a speculative microcap whose trial claims (the QIII pilot, anticipated 2027-01-01, and a patent update) are forecasts and filings rather than data, so they warrant skepticism.
Our read on the data ›
Signals we're tracking
EPKINLY Regulatory-Clinical Success Cascade
High probability of expanded label indications, additional combination approvals, and competitive positioning strength in follicular lymphoma market. Predicts positive commercial uptake and potential accelerated review for related indications.
Patterns we're watching ›
Where sources disagree
ING Group
Both facts record the same metric (shares_outstanding) for ING Group at the identical observation date (2025-12-31). FACT A states 2,902,437,688 shares; FACT B states 2,902 million shares (2,902,000,000). The difference is 437,688 shares (~0.015%). This is a genuine value conflict, though the discrepancy appears to result from FACT B rounding to the nearest million while FACT A provides the precise count.
We flag conflicts openly ›
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