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Source document· March 19, 2026

Solid Biosciences Reports Fourth Quarter and Full Year 2025 Financial Results and Provides Business Updates

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Solid Biosciences Reports Fourth Quarter and Full Year 2025 Financial Results and Provides Business Updates - Duchenne (SGT-003): Positive interim Phase 1/2 INSPIRE DUCHENNE data reported at the 2026 MDA Annual Meeting continued to suggest differentiated clinical, safety and tolerability profiles; SGT-003 has been gene…
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  • SGT-003 continued to be generally well tolerated in 41 participants dosed as of March 18, 2026

    60% confidence
  • 2026 will be a transformational year for Solid with multiple anticipated regulatory and clinical milestones

    60% confidence
  • Net proceeds from private placement will be used to fund ongoing pipeline development programs, business development activities, working capital and general corporate purposes

    60% confidence
  • First participant in ARTEMIS trial expected to be dosed in Q2 2026, with initial safety data anticipated in second half of 2026

    60% confidence
  • Company anticipates dosing first participant in Phase 3 IMPACT DUCHENNE trial in April 2026

    60% confidence
  • INSPIRE DUCHENNE interim data provided continuing evidence suggesting a disease-relevant treatment effect with robust microdystrophin expression, DAPC restoration, muscle integrity biomarker improvements, and cardiac function stabilization

    60% confidence
  • Additional meetings with FDA planned in H1 2026 for guidance on potential accelerated approval pathway for SGT-003

    60% confidence
  • Initial data from FALCON trial expected in second half of 2026, subject to participant enrollment

    60% confidence
  • We continue to build momentum across our portfolio, highlighted by updated interim INSPIRE DUCHENNE data presented at MDA, positive feedback from FDA Type C meeting on Phase 3 IMPACT DUCHENNE trial design, dosing of first participant in FALCON trial and completion of oversubscribed $240 million private placement

    60% confidence
  • SGT-003 could be a potential best-in-class investigational gene therapy for treatment of Duchenne based on design features including R16/17 domains and POLARIS-101 capsid

    60% confidence
  • SGT-212 was well tolerated with no treatment-related adverse events as of March 18, 2026

    60% confidence
  • Company's cash runway anticipated to extend into H1 2028 including net proceeds from $240 million private placement

    60% confidence

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Autumn 2026 Biopharma Catalyst Season: Late-Breaking Data, FDA Milestones and the Rise of AI-Designed Drugs
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A nossa leitura dos dados ›
Sinais que acompanhamos
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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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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