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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…
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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're seeing
Autumn 2026 Biopharma Catalyst Season: Late-Breaking Data, FDA Milestones and the Rise of AI-Designed Drugs
Late-September and early-October 2026 conferences (EASD, EADV, IGCS) brought a cluster of positive late-breaking trial readouts. These covered obesity and metabolic disease (Novo Nordisk's CagriSema), immunology (Lilly's EBGLYSS, tulisokibart) and oncology (Rina-S, Agenus BOT+BAL). Ahead lie hard regulatory catalysts, led by the 14 Nov 2026 FDA PDUFA date for ivonescimab. At the same time, Insilico-style AI-designed drugs such as rentosertib are showing anti-aging signals. That points to AI-driven drug discovery moving from concept toward clinical validation. Unrelated tech and regulatory items (Tesla Cybercab probe, xAI litigation, OpenAI agent incident) and the speculative QAIAx claims are peripheral to this story.
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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.
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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.
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