Serina Therapeutics, Inc. · AMEX:SER

Serina Therapeutics — Investor Presentation (September 2026)

20 slides from Serina Therapeutics's investor presentation, September 2026

  1. Slide 1: POZ Platform

    ® POZ Platform • Next Generation Drug Product Optimization Platform • Enabling Improvements of Multiple Drug Modalities CNS small molecule optimization – POZ / LNP - immune silent, payload POZ / ADC – enabling novel payloads / Lead asset in clinic agnostic delivery mechanisms Non-confidential invest

  2. Slide 2: Forward Looking Statements

    This presentation contains forward-looking statements that are based on management’s beliefs and assumptions and on information currently available to management. In some cases, you can identify forward-looking statements by the following words: “may,” “will,” “could,” “would,” “should,” “expect,” “

  3. Slide 3: Enabling better CNS medicines from proven molecules

    Enabling better CNS medicines from proven molecules SER-252 SER-270 SER-290 POZ-apomorphine POZ-DHTB / VMAT2i POZ-undisclosed Advanced Parkinson’s Tardive dyskinesia / Undisclosed CNS disease movement disorders indication Phase 1b study underway IND-enabling planning IND-enabling planning Lead asset

  4. Slide 4: Small Molecule Optimization: SER-252-led, milestone-driven CNS story

    Small Molecule Optimization: SER-252-led, milestone-driven CNS story Clinical-stage Proven-molecule FDA-aligned Near-term Repeatable lead asset strategy 505(b)(2) NDA de-risking CNS model path events SER-252 is in a Apomorphine is Known API, prior SAD data can address SER-270 and SER-290 registratio

  5. Slide 5: Why now: clinical execution and financing strengthened in 2026

    Why now: clinical execution and financing strengthened in 2026 SER-252 has moved from regulatory alignment into clinical execution with defined near-term milestones. SER-252 in clinic Next safety gate First patient dosed in February 2026 in SAD Cohort 1 blinded safety/tolerability/PK review SAD arm

  6. Slide 6: SER-252 at a glance

    SER-252 at a glance Lead product candidate designed to make continuous dopaminergic stimulation easier to deliver in advanced Parkinson’s disease. POZ-apomorphine Apomorphine is a clinically active dopamine agonist, but current continuous products are limited by pump burden and local administration-

  7. Slide 7: Advanced Parkinson's disease creates a defined unmet need

    Advanced Parkinson’s disease creates a defined unmet need As disease advances, oral regimens often become insufficient and patients move toward high-burden continuous therapies. The treatment journey creates a clear target population: More frequent OFF time and less predictable symptom control ~250K

  8. Slide 8: Continuous dopaminergic stimulation (CDS) is becoming a commercial category

    Continuous dopaminergic stimulation (CDS) is becoming a commercial category The market is being built by recently approved products, creating a clearer path for differentiated entrants. 2.5 ~$2.1B 2 ~$1.8B Existing launches validate demand for continuous therapy, while highlighting the 1.5 importanc

  9. Slide 9: Approved continuous therapies validate demand, but leave room for improvement

    Approved continuous therapies validate demand, but leave room for Market validation improvement Established continuous levodopa/carbidopa therapy. Subcutaneous continuous levodopa/carbidopa product. Apomorphine confirms clinical utility of continuous dopamine agonist delivery. Remaining limitation S

  10. Slide 10: SER-252 target product profile: simpler continuous therapy

    SER-252 target product profile: simpler continuous therapy The product is being designed to deliver continuous therapy through a compact on-body system with brief wear time. 2x weekly No tubing on-body delivery compact wearable device No visible needle ~10 minutes designed for simple use wear time p

  11. Slide 11: SER-252's convenience + tolerability profile stands apart from the approved options

    SER-252’s convenience + tolerability profile stands apart from the approved options SER-252 (investigational) Vyalev (Abbvie) Onapgo (Supernus) Duopa / Duodopa (Abbvie) Foscarbidopa/foslevodopa SC Mechanism POZ-apomorphine SC injection Apomorphine SC infusion Carbidopa/levodopa intestinal gel infusi

  12. Slide 12: SER-252's near-term data should begin answering the central questions that drive value creation

    Safety / Can early cohorts show an acceptable safety 01 Tolerability profile in advanced PD patients? SER-252’s near- PK Does SER-252 generate controlled exposure term data should Profile consistent with continuous dopaminergic stimulation? 02 begin answering the central Skin Tolerability Does NHP i

  13. Slide 13: POZ can turn known active drugs into differentiated products

    POZ can turn known active drugs into differentiated products The platform can re-engineer clinically understood molecules into more usable product profiles Known Active Drug POZ Conjugate Clinically validated molecule Drug attached to POZ through with established pharmacology. cleavable linkers and

  14. Slide 14: A development model designed to reduce risk and capital intensity

    A development model Known API, prior human POZ PK proof and FDA designed to reduce risk alignment form a layered de-risking stack. and capital intensity Biology PK / Platform Regulatory Device Commercial Risk Risk Risk Risk Risk Known apomorphine Prior SER-214 Phase FDA aligned on enFuse has CDS cat

  15. Slide 15: SER-252 Phase 1b registrational study is underway

    First patient dosed February 2026; Status Cohort 1 n=8 dosing completed July 2026 SER-252 Phase 1b registrational study is underway Design Randomized, double-blind, placebo-controlled SAD and MAD components. The study is designed to generate safety, tolerability, PK and exploratory clinical Up to fi

  16. Slide 16: Value-inflection milestones

    Value-inflection milestones Clinical, regulatory and product-development milestones reduce risk in sequence before approval Cohort 1/ SAD Data MAD EOP2 NDA SMC Review Package Data Interaction Path Initial safety and Early PK, dose Repeat dosing, Refines remaining Registration tolerability gate; beha

  17. Slide 17: SER-252 targets a large, underpenetrated opportunity

    SER-252 $1.8B $2.7B ~250K targets a large, base-case peak annual upside peak annual sales advanced PD patients underpenetrated sales opportunity in US/EU4+UK opportunity if SER-252 further expands the inadequately controlled on oral therapy in advanced PD target market US/EU4+UK opportunity Clinical

  18. Slide 18: Key clinical translation question: can SER-252 avoid apomorphine infusion limitations?

    Why this matters Apomorphine is clinically active, but continuous infusion has been limited by short half-life, daily pump burden and serious local Key clinical administration-site reactions. translation question: Preclinical differentiation signal can SER-252 avoid NHP studies in company materials

  19. Slide 19: Execution support: pipeline repeatability, financing and leadership

    Execution support: SER-252 remains the priority; follow-on assets, recent financing and experienced leadership support pipeline repeatability, the next chapter. financing and leadership PIPELINE FINANCING SER-252 SER-270 SER-290 $21.2M POZ-apomorphine POZ-DHTB / VMAT2i POZ-undisclosed March/April 20

  20. Slide 20: SER-252 first; platform upside without loss of focus

    SER-252 first; platform upside without loss of focus Serina is a lead-asset execution story supported by a repeatable product-optimization platform. What Matters Now Serina builds better CNS medicines from proven Cohort 1 safety/tolerability blinded SMC review and advancement to Cohort 2 approved mo

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