MediWound is a fully integrated biopharmaceutical company focused on developing, manufacturing, and commercializing novel therapeutics based on its patented proteolytic enzyme technology that addresses unmet needs in the fields of severe burns, chronic, and other hard-to-heal wounds. MediWound was founded in 2001 and is based in Israel.
Country/Area :Israel
Company Email :contact@mediwound.com
Industry :BiotechnologyGifts & CraftsElectronicsHealthcareSchool & Office SuppliesPharmaceuticals
Company website :*****
Company phone :+972 779714100
Established :2001
Company Revenue :$20,934,000
Number of employees :67
SIC Code :28283
NAICS Code :54541
Main Products :MediWound Announces the Appointment of Hani Luxenburg as Chief Financial OfficerMediWound Announces Collaboration with Mölnlycke on EscharEx® Phase III StudyMediWound Announces Collaboration with 3M on EscharEx® Phase III StudyMediWound Receives Positive Scientific Advice from European Medicine Agency (EMA) on EscharEx Phase III Study DesignMediWound Announces U.S. Food and Drug Administration Approval of NexoBrid® for the Treatment of Pediatric Patients with Severe Thermal BurnsMediWound Announces Positive Results in Head-to-Head Comparison of EscharEx® vs. SANTYL® within the ChronEx Phase II Randomized Controlled StudyMediWound to Report First Quarter 2024 Financial ResultsMediWound Reports First Quarter 2024 Financial Results and Provides Company UpdateMediWound’s NexoBrid® Highlighted in 20 Oral and Poster Presentations at the 20th European Burns Association CongressMediWound Reports Second Quarter 2024 Financial Results and Provides Company UpdateMediWound Secures Additional U.S. Department of Defense Funding to Advance NexoBrid® Development for the U.S. ArmyMediWound Announces a Collaboration with PolyMedics Innovations (PMI) for NexoBrid® Distribution in EuropeMediWound Announces Collaboration with MIMEDX on EscharEx® Phase III StudyMediWound Announces $25 Million Strategic Private Placement FinancingMediWound Reports Second Quarter 2023 Financial Results and Provides Company UpdateMediWound Announces Appointment of Shmulik Hess, Ph.D. as Chief Operating Officer and Chief Commercial OfficerMediWound to Report Second Quarter 2024 Financial ResultsMediWound Announces €16.25 Million Funding from the European Innovation Council Accelerator ProgramMediWound to Report Second Quarter 2023 Financial ResultsMediWound to Report First Quarter 2023 Financial ResultsMediWound to Participate in Fireside Chat at H.C. Wainwright 25th Annual Global Investment ConferenceMediWound Announces Positive Results in Its U.S. Phase I/II Study of MW005 for the Treatment of Basal Cell CarcinomaMediWound Announces that FDA has Accepted for Review the Supplement to the NexoBrid BLA to Include Pediatric Patients with Severe Thermal BurnsMediWound Deploys NexoBrid® for Emergency SupplyMediWound to Report Third Quarter 2023 Financial ResultsMediWound Announces Peer-Reviewed Publication of EscharEx® Mechanism of Action Study Assessing Its Effects on Biofilm and Microbial LoadsMediWound Announces Commercial Launch of NexoBrid® in JapanMediWound Reports Fourth Quarter and Full Year 2022 Financial Results and Company UpdateMediWound Announces an Additional $10 Million Award from BARDAMediWound to Participate in Fireside Chat at Maxim Group Healthcare Virtual Conference 2023MediWound to Participate in Two Upcoming Investor ConferencesMediWound Reports Third Quarter 2023 Financial Results and Provides Company UpdateMediWound to Present Phase 2 EscharEx® Data at the Symposium on Advanced Wound Care (SAWC) Spring 2023MediWound to Report Fourth Quarter and Full Year 2023 Financial ResultsMediWound Reports First Quarter 2023 Financial Results and Provides a Company UpdateMediWound Receives Positive CHMP Opinion Recommending Approval for NexoBrid® to Treat Pediatric PatientsMediWound Reports Fourth Quarter and Full Year 2023 Financial Results and Provides Company UpdateMediWound Announces Publication of the EscharEx® Phase II ChronEx Study Results for Venous Leg UlcersMediWound to Present New Data from EscharEx® Phase II Studies at Three Leading Wound Care Conferences