Cyclerion Therapeutics, Inc. · NASDAQ:CYCN

Cyclerion Therapeutics — Korsana Biosciences — Merger or Acquisition (July 2026)

32 slides from Cyclerion Therapeutics's merger presentation, July 2026

  1. Slide 1: Korsana Biosciences Overview

    Korsana Biosciences Overview July 2026

  2. Slide 2: Disclaimers

    Disclaimers The information contained in this presentation has been prepared by Korsana Biosciences, Inc. and its affiliates (“Korsana” or the “Company”) and contains information pertaining to the business and operations of the Company and the proposed reverse merger transaction with Cyclerion Thera

  3. Slide 3: Disclaimers

    Disclaimers No Offer or Solicitation This presentation and the information contained herein is not intended to and does not constitute (i) a solicitation of a proxy, consent or approval with respect to any securities or in respect of the proposed transactions or (ii) an offer to sell or the solicita

  4. Slide 4: Korsana is developing potentially best-in-class therapies, with initial focus on neurodegenerative disorders

    Korsana is developing potentially best-in-class therapies, with an initial focus on neurodegenerative disorders  Initially focused on potentially best-in-class therapies for neurodegenerative disorders like Alzheimer’s disease  Built on Therapeutic Targeting (THETA ), our next-generation BBB-penet

  5. Slide 5: Korsana is founded on four key beliefs

    Korsana is founded on four key beliefs Alzheimer's is a Shuttling is the Korsana has the Korsana has a rapid vast and de-risked best way to improve potential best-in-class path to value creation opportunity existing agents approach For the first time, there is a Transferrin receptor (TfR)-based Lead

  6. Slide 6: Alzheimer's is a vast and de-risked opportunity

    Alzheimer’s is a vast and de-risked opportunity

  7. Slide 7: Alzheimer's is a devastating neurological disorder with significant unmet need

    Alzheimer’s is a devastating neurological disorder with significant unmet need and a rapidly growing patient population The number of Americans with Alzheimer’s is projected to nearly double by 2050 Age 65+ US population (M) Total annual cost of care in US Alzheimer’s patients $1T 100 Other 65+ popu

  8. Slide 8: Today's anti-Aβ therapies leave significant room for improvement

    Despite clinical progress and approvals, today’s anti-Aβ therapies leave significant room for improvement Approved therapies only demonstrate ~30% slowing …and carry black box warnings for ARIA of disease progression at 18 months… risk, affecting ~15-25% of treated patients Months Months 0 3 6 9 12

  9. Slide 9: Approved therapies are highly inconvenient, with IV dosing and MRI monitoring

    Approved therapies are also highly inconvenient, with onerous IV dosing and MRI monitoring on label Month BL 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 Dosing Monitoring As needed for ARIA symptoms Dosing Monitoring As needed for ARIA symptoms 9 Notes: BL: baseline. Patients can be taken off Kisun

  10. Slide 10: Amyloid reduction predicts slowing of cognitive decline

    First-gen therapies have laid out the roadmap for success: amyloid reduction predicts slowing of cognitive decline 0.2 0.0 “The Agency has found… that reduction of brain Aβ plaque on PET is Lower score is better -0.2 reasonably likely to predict clinical benefit in Alzheimer’s disease.” Cognitive De

  11. Slide 11: Shuttling is the best way to improve existing agents

    Shuttling is the best way to improve existing agents

  12. Slide 12: Shuttling ferries large molecules across the blood-brain barrier

    Shuttling approaches actively ferry large molecules across the blood-brain barrier (BBB), fundamentally changing CNS penetration Capillary Brain parenchyma Shuttle-enabled mAb Receptor- Transferrin receptor mediated transcytosis Endothelial cell Amyloid plaque 12 Notes: Figure made in BioRender. Ada

  13. Slide 13: Trontinemab shows significant efficacy improvement over gantenerumab

    Roche’s trontinemab, the first shuttled anti-Aβ antibody, has shown a significant efficacy improvement over first-gen gantenerumab… Trontinemab shows ~8x increased CSF … and most trontinemab-treated Alzheimer’s patients exposure over gantenerumab in humans… reached “amyloid-negative” status by W28 C

  14. Slide 14: Trontinemab greatly reduces ARIA

    … and greatly reduces ARIA, the critical safety signal for this class of therapies ARIA rate (%) 30 ARIA-E ARIA-H 26% 25 24% 24% 24% 22% 20 20% 17% 15 13% 10 7% 5 4% 3% 1% 0 Trontinemab Trontinemab Gantenerumab Gantenerumab Lecanemab Donanemab (1.8 mg/kg, N=76) (3.6 mg/kg, N=73) (GRADUATE 1, N=503)

  15. Slide 15: Trontinemab's profile leaves headroom for competitive differentiation

    However, as a first-gen shuttled Aβ, trontinemab’s profile leaves substantial headroom for competitive differentiation Efficacy Safety Dosing & Tolerability Mean amyloid plaque reductions from baseline Mean hemoglobin changes from baseline Incidence of infusion related reactions Adj. change from bas

  16. Slide 16: Korsana has the potential best-in-class approach

    Korsana has the potential best-in-class approach

  17. Slide 17: Korsana's goal is a best-in-class shuttled Aβ therapy

    Korsana’s goal is to achieve a best-in-class shuttled Aβ therapy, offering meaningful improvements over trontinemab Key Value Drivers for KRSA-028 FAST, ROBUST Efficacy on par or greater than trontinemab AMYLOID REDUCTIONS DIFFERENTIATED Minimal ARIA risk, avoid hematologic AEs SAFETY PROFILE CONVEN

  18. Slide 18: KRSA-028 is a next-gen shuttled anti-Aβ

    KRSA-028 is a next-gen, potentially best-in-class shuttled anti-Aβ Pyroglutamate-Aβ Subcutaneous formulation targeted backbone • Expected to be efficacious at lower dose • Targets the Aβ epitope associated with than first-generation shuttled therapies the greatest amyloid plaque clearance • Optimize

  19. Slide 19: Targeting pyroglu-Aβ epitope delivers promising clinical efficacy in Phase 3

    Targeting the plaque-specific pyroglu-Aβ epitope has been shown to deliver the most promising clinical efficacy in Phase 3 trials Amyloid plaque clearance and Ph3 clinical performance of Aβ antibodies Antibody Aβ epitope / species targeted 0.4 CDR-SB adjusted mean difference from placebo 0.2 Aducanu

  20. Slide 20: KRSA-028 targets plaque-selective pyroglu-Aβ to maximize clearance

    KRSA-028 targets plaque-selective pyroglu-Aβ to maximize plaque clearance through phagocytosis KRSA-028 exhibits potent pyroglu-Aβ phagocytosis KRSA-028 Aβ backbone:  Same plaque-selective epitope Cellular Uptake as donanemab and remternetug 3pE-Aβ (3-42) fibrils 40 KRSA-028  High Aβ affinity, KD

  21. Slide 21: KRSA-028 has longer half-life and avoids reticulocyte depletion in NHPs

    KRSA-028 has a longer half-life than trontinemab and avoids reticulocyte depletion in NHPs KRSA-028 has >2.5x half-life in NHPs KRSA-028 avoids reticulocyte depletion in NHPs compared to trontinemab 1000 400 300 from baseline) Baseline) 200 (μg/mL) concentration (µg/mL) 100 100 Change from Concentra

  22. Slide 22: KRSA-028 shows improved brain penetration in mouse and NHP

    KRSA-028 shows improved brain penetration in mouse and NHP KRSA-028 demonstrates increased brain KRSA-028 shows >6x brain penetration in NHPs penetration in hTfR1/hFcRn mouse model compared to trontinemab 40 40 KRSA-028 KRSA-028 KRSA-028 30 Concentration 30 Trontinemab Trontinemab Brain Concentratio

  23. Slide 23: KRSA-028 expected to match trontinemab exposure with low volume SC

    KRSA-028 is expected to match trontinemab Phase 3 IV exposure with low volume SC, compatible with autoinjector Projected human PK • PK model suggests that KRSA-028 will match trontinemab Phase 3 exposure with a monthly SC volume of 1-2 mL Serum concentration (µg/mL) KRSA-028 Cavg Trontinemab Cavg •

  24. Slide 24: KRSA-028 preclinical data accelerate and de-risk development

    Novel Aβ and TfR1 binding sequences retain key features of clinically validated molecules High affinity pyroglu-Aβ binding and clearance via ADCP leverage best- proven mechanism of efficacy We believe KRSA- 028 preclinical data TfR1 binding matches trontinemab epitope with similar affinity, accelera

  25. Slide 25: Korsana has a rapid path to value creation

    Korsana has a rapid path to value creation

  26. Slide 26: PET imaging provides rapid proof of concept and dose-ranging

    PET imaging in early clinical development provides rapid proof of concept and dose-ranging for amyloid plaque clearing Trontinemab Phase 1/2: Remternetug Phase 1: Robust dose-response by Day 50 Robust dose-response by Day 85 N=7 N=5 N=10 N=4 N=10 N=5 We believe KRSA-028 amyloid PET data – achievable

  27. Slide 27: Scientific innovations and market dynamics driving Alzheimer's treatment inflection

    A confluence of scientific innovations and market dynamics are driving Alzheimer’s treatment to a major inflection point Despite a slower than expected launch, Upcoming catalysts in presymptomatic AD sales of Aβ therapies are accelerating may lead to rapid market expansion • Improved dose regimens (

  28. Slide 28: KRSA-028 Phase 1/2 trial designed to rapidly deliver data

    KRSA-028 Phase 1/2 trial: designed to rapidly deliver potentially differentiating data Trial design: Single Ascending Dose in healthy volunteers, with integrated Multiple Ascending Dose in Alzheimer’s disease patients, and expansion cohorts designed to enable Phase 3 Part 1 SAD in HV Part 2 MAD in A

  29. Slide 29: Korsana is well-funded through multiple clinical milestones

    Korsana is well-funded through multiple clinical milestones 2H 26 1H 27 2H 27 1H 28 Move quickly to dose KRSA-028 ranging & expansion File File Healthy Patient PoC cohorts, intended to Anti-3pE amyloid CTN IND Volunteer Data Biomarker Data beta mAb support rapid (THETA-enabled) (YE26) (1Q27) (mid-27

  30. Slide 30: Korsana is poised for rapid progress

    Korsana is poised for rapid progress Near-Term Catalysts Well-Financed Experienced Leadership KRSA-028 • $25M seed round Q4 2024 • Seasoned CEO Jonathan Violin • CTN filing expected YE26 • $150M Series A Sept 2025 • Prior CEO roles include: • IND filing expected 1Q27 • $380M PIPE, expected to Viridi

  31. Slide 31: Estimated capitalization following reverse merger and pre-closing financing

    Estimated capitalization following close of reverse merger & pre- closing financing Shares on an Expected ownership of the as-converted basis combined company CYCLERION THERAPEUTICS • Shares of common stock outstanding 4,681,351 1.1% (including underlying options, preferred & RSAs) • Shares of commo

  32. Slide 32: Thank you

    WA KORSANA MB BIOSCIENCES Thank you

Korsana Biosciences — Merger or Acquisition (July 2026) on 6ix