Gh Research Plc · NASDAQ:GHRS

Gh Research — Investor Presentation (November 2024)

15 slides from Gh Research's investor presentation, Nov 14, 2024

  1. Slide 1: November 2024 Corporate Presentation

    GH Research PLC (NASDAQ: GHRS) November 2024 Corporate Presentation 1

  2. Slide 2: Disclaimer and forward-looking statements

    This presentation has been prepared by GH Research PLC (“GH Research”) for informational purposes only and not for any other purpose. Nothing contained in this presentation is, or should be construed as, a recommendation, promise or representation by the presenter or GH Research or any director, emp

  3. Slide 3: Stage of Development

    Stage of Development PROGRAMS INDICATION PRECLINICAL PHASE 1 PHASE 2a PHASE 2b PHASE 3 CURRENT STATUS MILESTONES GH001Mebufotenin for inhalation administration Treatment-Resistant Depression (TRD) Phase 2b RDBPC DB phase completed Phase 1 PK trial with proprietary device ongoing Phase 2b OLE complet

  4. Slide 4: The Problem for Patients with Depression

    The Problem for Patients with Depression Established Therapies are Slow-Acting ... Remission Rates in TRD < 15% 4 (STAR*D study, Remission Rate Over Time, Treatment Step 1 = Citalopram) (STAR*D study, Remission Rates Treatment Steps 1 to 4) Average time to remission is ~6 weeks 2 or more prior thera

  5. Slide 5: Large and Open Depression Market in the EU and US

    First Line MDD Second Line MDD Treatment-Resistant Depression (TRD) Patients cycle through ineffective therapies for TRD Diagnosed: ~48M Treated (pharmacotherapy ± psychotherapy): ~24M Non-response to first line: ~13M Non-response to two prior lines: ~9M Large and Open Depression Market in the EU an

  6. Slide 6: SPRAVATO has been established as a $1-5Bn drug in interventional psychiatry

    SPRAVATO® has been established as a $1-5Bn drug in interventional psychiatry Quarterly sales, $M; Estimated annual WAC of $32,400 Estimated 40 administration visits per year: In-clinic Mandatory 2-hour post-dose monitoring No driving or operating heavy machinery until next day No psychotherapeutic i

  7. Slide 7: The GH001 Aspirational Profile

    The GH001 Aspirational Profile Maximize Day 2 Response Rate ✔✔✔✔ ✔ Maximize Day 8 Response Rate ✔✔✔✔ ✔ Minimize In-Clinic, Post-Administration Monitoring ≤ 1 hour ≥ 2 hours Minimize Post-Discharge Restrictions None No driving or operating machinery until the next day after a restful sleep Optimize F

  8. Slide 8: 80% less patient time required with GH001

    80% less patient time required with GH001 8 GH001 Based on ICER estimate Based on Phase 2b trial design Abbreviations: ICER = Institute for Clinical and Economic Review Sources: 1) Johnson & Johnson Spravato Access, Coding and Reimbursement Guide; 2) ICER Spravato Final Evidence Report; 3) Janssensc

  9. Slide 9: Completed GH001 Clinical Trials: Trial Design

    GH001-HV-1032 (Healthy Volunteers) GH001 6 mg (n=8+2 placebo) GH001 12 mg (n=8+2 placebo) GH001 18 mg (n=8+2 placebo) GH001 IDR (6, 12, 18 mg)up to 3 doses, 1h interval (n=8) GH001 IDR (6, 12, 18 mg) up to 3 doses, 2h interval (n=8) 9 Completed GH001 Clinical Trials: Trial Design GH001-HV-1011 (Heal

  10. Slide 10: GH001-TRD-102 | Efficacy of the GH001 IDR

    GH001-TRD-102 | Efficacy of the GH001 IDRPhase1/2 trial of GH001 in TRD (completed) 10 Abbreviations: MADRS = Montgomery–Åsberg Depression Rating Scale; IDR = Individualized dosing regimen aBaseline mean MADRS = 32. Sources: 1) Reckweg JT, et al. Front. Psychiatry. 2023. Hour 2 Day 1 Day 7 GH001 p=0

  11. Slide 11: Safety and Tolerability of GH001 in Completed Trials

    Safety and Tolerability of GH001 in Completed TrialsGH001-HV-1011, GH001-HV-1032, and GH001-TRD-1023 11 Safety Parameters, n (% of population) Overall Population (n=78) Any TEAE 50 (64%) Headache 19 (24%) Anxiety 12 (15%) Nausea 8 (10%) Fatigue 7 (9%) Any Serious AE 0 (0%) Any AE leading to trial/dr

  12. Slide 12: Phase 2b Trial in Treatment-Resistant Depression GH001-TRD-201

    (Initiated) Phase 2b Trial inTreatment-Resistant DepressionGH001-TRD-201 12 EudraCT Number: 2022-000574-26

  13. Slide 13: GH001-TRD-201 Trial Design

    GH001-TRD-201 Trial DesignPhase 2b trial in patients with TRD, n=801 13 Abbreviations: D = Day; h = Hour; BL = Baseline; IDR = Individualized dosing regimen; M = Month; MADRS = Montgomery–Åsberg Depression Rating Scale; OLE = Open-label extension; TRD = Treatment-resistant depression. a The double-b

  14. Slide 14: Three-Layer Protection Strategy

    Three-Layer Protection Strategy 14 LAYER 1: REGULATORY EXCLUSIVITY FDA: 5 years (+2.5 years paragraph IV stay) EMA: 10 years (+1 year for new indication) LAYER 2: PATENTS Granted patents and patent applications relating to mebufotenin, including: Novel uses in various disorders (including inhaled, n

  15. Slide 15: Board of Directors & Executive Management

    Board of Directors & Executive Management 15 Florian Schönharting Michael Forer MSc Chairman of the Board, Co-founder BA, LLB Vice-Chairman of the Board Dermot Hanley Duncan Moore BSc, MBA Board Member MPhil, PhD Board Member Julie Ryan FCA, MAcc, BComm VP, Finance Magnus Halle BSc Managing Director

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