Mediwound Ltd. · NASDAQ:MDWD
Mediwound — Investor Presentation (August 2025)
29 slides from Mediwound's investor presentation, August 2025
Slide 1: Next-Generation Enzymatic Therapeutics for Non-Surgical Tissue Repair
Next-Generation Enzymatic Therapeutics for Non-Surgical Tissue Repair August 2025 I Nasdaq: MDWD
Slide 2: Cautionary Note Regarding Forward-Looking Statements
Cautionary Note Regarding Forward-Looking Statements This presentation contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act and other securities laws, including but not limited to the statements related to the commercial potential of our products a
Slide 3: MediWound Company Highlights
MediWound Company Highlights Multibillion dollar Validated enzymatic Strategic global commercial opportunity technology platform collaborations 14 successful clinical trials Vericel, Mölnlycke, Kaken, MIMEDX, NexoBrid® 120+ peer-reviewed publications BARDA, EIC, DoD, PolyMedics, Mankind, Eschar remo
Slide 4: Core Platform – Enzymatic Biologics for Tissue Repair
Core Platform – Enzymatic Biologics for Tissue Repair Proprietary IP protected manufacturing process Pineapple stem Protein harvest extraction Purification, enrichment, Complex mixture of stabilization proteolytic enzymes 4
Slide 5: Multi-Billion Dollar Portfolio
Multi-Billion Dollar Portfolio NexoBrid® EscharEx® Disruptive therapy for burn care Investigational Next-Gen enzymatic therapy for wound care Indication: Eschar removal in deep-partial and full thickness burns Targeted indication: Debridement of chronic/hard-to-heal wounds Classification: Orphan bio
Slide 6: Product Pipeline
Product Pipeline Indication Development Phase 1 Phase 2 Phase 3 Registration Marketed Adult burn eschar removal Approved Pediatric burn eschar removal Approved Collaborations: Battlefield burn eschar removal DoD1 funded Blast injury treatment POC2 EscharEx ® VLU debridement Interim assessment mid-20
Slide 7: Value Creating Milestones
Value Creating Milestones 2025 2026 VLU Phase 3 FDA/EMA DFU PK study VLU Phase 3 initiation protocol discussions interim EscharEx® Strategic research H2H vs. DFU trial Human VLU Phase 3 collaborations collagenase initiation Factor study last patient out U.S. facility: BARDA-funded FDA/EMA scale-up N
Slide 8: Financial Highlights
Financial Highlights BALANCE SHEET REVENUE EQUITY $33M in cash1 2024 revenue of $20M Outstanding shares: 11.0M2 NexoBrid® is profitable Fully diluted: 14.8M No debt Scale-up will potentially increase gross margin to 65% $115M+ received from BARDA $16M funded by DoD • Josh Jennings, MD – TD Cowen • S
Slide 9: Early, effective and selective non-surgical eschar removal for severe burns
Early, effective and selective non-surgical eschar removal for severe burns (8.8% concentration) Validated & commercialized Approved in 40+ countries including US, EU, JP; 15,000+ patients treated to date
Slide 10: Eschar Removal - Critical First Step in Burn Care
Eschar Removal - Critical First Step in Burn Care Removal of non-viable tissue is Surgical removal of eschar is critical for wound healing1 traumatic & non-selective2,3 Eschar Prevents infection Stops deterioration Reveals tissue for Loss of healthy tissue Challenging Requires surgical team, and sep
Slide 11: NexoBrid - Non-Surgical, Selective, Effective
NexoBrid® - Non-Surgical, Selective, Effective Indication: Eschar removal of deep partial-thickness and/or full-thickness thermal burns Commercial availability: US (Vericel), Japan (Kaken), Europe (direct, and PMI), India (Mankind) Government support: $115M+ received from BARDA & DoD Contracts Eas
Slide 12: Phase 3 Studies Demonstrated Superiority Over SOC
Phase 3 Studies Demonstrated Superiority Over SOC1 Incidence of complete Time to complete Incidence of surgical Blood loss eschar removal eschar removal eschar removal (days) 815ml 814.51ml 93.3% 72% 100% p<0.0001 p<0.0001 p <0.0001 p<0.0001 50% 4.0% 4% 14ml 0% 0 10 20 30 40 NexoBrid N=75 SOC N=75 N
Slide 13: Facility Scale-Up Supports Future Growth
Facility Scale-Up Supports Future Growth Full manufacturing capacity anticipated in 2026 NexoBrid® target revenue ($M) 35.0 32-342 28-302 30.0 2023 2024 20251 2026 24-26 Planning and 25.0 Initiation 20 20.0 Construction 15.0 FDA/EMA Submissions 10.0 6X Capacity Increase1 EU US 5.0 0.0 2024 2025 (E)
Slide 14: Next-Generation Enzymatic Debridement Candidate for Chronic Wounds
Next-Generation Enzymatic Debridement Candidate for Chronic Wounds (5% concentration) Superior to SOC - Clinically de-risked - validated technology $2.5B TAM opportunity aims to set a new bar for efficacy and successful Phase 2 trials
Slide 15: EscharEx Targets Lower Extremity Chronic Ulcers
EscharEx® Targets Lower Extremity Chronic Ulcers Venous leg ulcers Diabetic foot ulcers (VLU) (DFU) Underlying pathology Chronic venous insufficiency Diabetes (Type I/II) Affected area Lower leg or ankle Mostly bottom of the foot Ulcer characteristics Large, shallow ulcers; moderate/severe pain Smal
Slide 16: Current Debridement Treatments are Sub-Optimal
Current Debridement Treatments are Sub-Optimal Modalities by efficacy and complexity Modalities by ulcer type (U.S.)1 100% 2% 3% 3% Other Surgical EscharEx® 3% 15% 7% 3% Mechanical Only Ultrasonic 80% 1% 4% 10% 5% Non-sharp Combo 5% 9% (without Enzymatic) Biological 60% 1% Sharp + Autolytic 11% Effi
Slide 17: EscharEx Achieves Enzymatic Debridement within Days
EscharEx® Achieves Enzymatic Debridement within Days Target Indication: Rapid debridement and promotion of healthy granulation tissue (Wound Bed Preparation1) in chronic and hard-to-heal wounds Status: Investigational drug Debrides chronic ulcers within 4-8 daily administrations2 Reduces bacteri
Slide 18: Three Phase 2 Studies Show Robust and Consistent Results
Three Phase 2 Studies Show Robust and Consistent Results WEEKLY SCREENING DAILY FOLLOWUP NON-SURGICAL SOC 2w 14w EscharEx n=46 RANDOMIZATION ChronEx1 Placebo n=43 ✓ Debridement VLU ✓ Wound Bed Preparation SOC n=30 ✓ Debridement ✓ Wound Bed Preparation PharmEx2 EscharEx n=12 ✓ Wound size reduction VL
Slide 19: Phase 2 MW-EX01 Trial: EscharEx Effective in Both VLU and DFU
Phase 2 MW-EX01 Trial: EscharEx® Effective in Both VLU and DFU Incidence of complete debridement (VLU, DFU, Traumatic ulcers) 93% of the patients who 55% completed debridement with EscharEx®, achieved full 29% debridement within 7 days p = 0.04 (4-5 daily applications) EscharEx Placebo n = 49 n = 24
Slide 20: Phase 2 ChronEx Trial in VLU: Endpoints Significantly Met
Phase 2 ChronEx Trial in VLU: Endpoints Significantly Met Complete debridement within 2 weeks Time to wound bed prepared (primary endpoint) 63% p < 0.001 p = 0.004 30% 13% p = 0.011 p = 0.004 EscharEx® Placebo NSSOC n = 46 n = 43 n = 30 EscharEx 63% vs. placebo 30% EscharEx 11 days vs. placebo 85 da
Slide 21: Phase 2 PharmEx Trial: EscharEx Surpasses Traditional Debridement
Phase 2 PharmEx Trial: EscharEx® Surpasses Traditional Debridement 70% 64% 35% 100% Complete debridement achieved Bioburden reduced Wound size reduced by end Biofilm substantially reduced within 8 applications by end of treatment of two-week follow-up for all patients positive for (avg 3.9 applicati
Slide 22: EscharEx Well-Positioned to Become Market Leader
EscharEx® Well-Positioned to Become Market Leader EscharEx® SANTYL Approved in 1965; $372M annual revenues (2023) Investigational drug - Phase 3 Existing reimbursement code1 Mixture of enzymes; multiple targets of action Collagenase; single target of action Debridement, promotion of granulation, red
Slide 23: Head-to-Head Data Shows EscharEx Superiority vs. SANTYL
Head-to-Head Data Shows EscharEx® Superiority vs. SANTYL1 Incidence of complete Time to achieve WBP Time to wound closure Patient-reported pain debridement in 2 weeks p=0.05 p=0.014 p=0.001 Consistent results in pediatric Phase 3 study, EU Phase 3 study and post marketing data2 1. Dove et al., 2025;
Slide 24: EscharEx VALUE Phase 3 Trial in VLU Patients
EscharEx® VALUE Phase 3 Trial in VLU Patients STUDY DESIGN ENDPOINTS A global (US, EU, ROW), randomized, double blind, adaptive design study in VLU patients Co-primary: Incidence of complete debridement STUDY Two arms: EscharEx vs. placebo, 1:1 ratio Incidence of complete wound closure OBJECTIVES Sa
Slide 25: EscharEx Head-2-Head Phase 2 Trial in VLU Patients
EscharEx® Head-2-Head Phase 2 Trial in VLU Patients STUDY DESIGN ENDPOINTS A global (US, EU) prospective, randomized, double blind study in VLU patients Primary: • Safety and tolerability STUDY Three arms: EscharEx vs. placebo vs. collagenase1 • Change in pain OBJECTIVES 1:1:1 ratio • Infection rate
Slide 26: Primary Research: EscharEx to Transform the Market
Primary Research: EscharEx® to Transform the Market All care settings report strong drivers for adoption1 EscharEx draws share across all debridement modalities1,5 SANTYL 2 18% 30% EscharEx 3 4 Ease of use Reduced treatment duration Reduction readmission risk Accelerated wound healing Reimbursement
Slide 27: $725M Projected Peak Sales in $2.5B TAM in U.S.
$725M Projected Peak Sales in $2.5B TAM in U.S. DFU & VLU prevalence ~4.10M Estimated 2028 total patient population 2.42M DFU and 1.68M VLU, (4.10M total)1 DFU: 2.42M VLU:1.68M DFU & VLU patients that require debridement ~2.98M Percent of patients undergoing debridement quantified through survey and
Slide 28: Experienced Leadership Team
Experienced Leadership Team Nachum (Homi) Shamir Ofer Gonen Dr. Shmulik Hess Dr. Ety Klinger Barry Wolfenson Hani Luxenburg Dr. Robert J. Snyder Chairman CEO COO & CCO Chief R&D Officer EVP Strategy & Corp Dev. CFO CMO 28
Slide 29: Strategic Timeline
Strategic Timeline NexoBrid EscharEx VLU Phase 3 EscharEx VLU Phase 3 EscharEx $24-26M revenue Interim assessment results FDA approval EscharEx VLU Phase 3 EscharEx DFU Trial EscharEx BLA filing U.S. based initiation initiation manufacturing facility Strategic research EscharEx vs. collagenase NexoB