Mediwound Stock Price, News & Analysis

MediWound Ltd. (Nasdaq: MDWD) is a global biotechnology company focused on developing and commercializing enzymatic, non-surgical therapies for tissue repair. According to company disclosures, MediWound’s core activities center on therapies for the enzymatic removal of eschar in thermal burns and the debridement of chronic and other hard-to-heal wounds. The company is listed on Nasdaq and is described as a global biotechnology company with operations and manufacturing in Yavne, Israel.

Core Products and Pipeline

MediWound’s first commercial biopharmaceutical product is NexoBrid®, an FDA-approved biological orphan drug indicated for the enzymatic removal of eschar in patients with deep partial- and full-thickness thermal burns. Company materials state that NexoBrid selectively removes non‑viable tissue while preserving viable tissue and is approved for use in adults and pediatric patients in over 40 countries, including the United States, European Union, Japan, and additional international markets. NexoBrid is marketed in these regions and is supported by clinical and real‑world data presented in scientific forums and peer‑reviewed publications.

The company is also advancing EscharEx®, a late‑stage investigational therapy for the debridement of chronic wounds. EscharEx is being evaluated in the global VALUE Phase III trial in venous leg ulcers, targeting 216 patients across sites in the U.S. and Europe. Company updates describe EscharEx as an investigational therapy that has demonstrated clinical advantages over the leading enzymatic debridement product and that targets a substantial global market opportunity in chronic wound management. MediWound has reported plans for additional studies in diabetic foot ulcers and pressure ulcers, as well as investigator‑initiated research.

Therapeutic Focus and Technology

Across its portfolio, MediWound describes itself as pioneering enzymatic, non‑surgical therapies for tissue repair. Its products are designed to remove damaged tissue in a controlled manner without traditional surgical excision. In the burn setting, NexoBrid is indicated for enzymatic eschar removal in thermal burns. In chronic wounds, EscharEx is being developed as an enzymatic debridement option. Company communications emphasize the selective action of these therapies on non‑viable tissue and their role in preparing wound beds for subsequent care.

Manufacturing and Operational Platform

MediWound develops and manufactures its enzymatic biologics and has invested in expanding its production capabilities. The company reports that it has completed commissioning and expansion of a GMP manufacturing facility for NexoBrid in Yavne, Israel, engineered to increase production capacity by approximately sixfold. The expanded facility is described as fully operational, with commercial availability of product from this site subject to completion of regulatory reviews and approvals in relevant markets.

Through this manufacturing platform, MediWound aims to support growing global demand for NexoBrid across more than 40 approved markets and to underpin future launches in additional geographies, subject to regulatory processes. Company disclosures also reference planning for future U.S.-based manufacturing of NexoBrid under a BARDA‑funded initiative.

Geographic Reach and Commercialization

According to company statements, NexoBrid is marketed in the United States, European Union, Japan, Australia, and other international markets. In the U.S., NexoBrid is commercialized through an exclusive partnership with Vericel, which reports on hospital adoption, burn center utilization, and reimbursement‑related initiatives such as pursuit of a permanent CPT code. Outside the U.S., MediWound works with regional partners, including an exclusive partner in Australia for marketing and distribution following approval by the Therapeutic Goods Administration.

While NexoBrid is the company’s commercial product, EscharEx remains an investigational therapy in late‑stage development. Company materials describe EscharEx as targeting chronic wound indications and note collaborations with multiple global wound care companies to support clinical trials and potential future market access.

Research, Clinical Development, and Collaborations

MediWound invests in clinical research to support both its approved product and pipeline. For NexoBrid, the company has highlighted prospective clinical data evaluating its use in traumatic tattoos following abrasion and blast injuries, with results published in a peer‑reviewed journal. These data examined the reduction of embedded particles and pigmented wound surface after enzymatic debridement with NexoBrid in patients with friction and blast injuries.

For EscharEx, MediWound is conducting the VALUE Phase III trial in venous leg ulcers and has reported post‑hoc analyses from Phase II data in a peer‑reviewed journal focused on wound bed preparation and healing predictors. The company has also announced collaborations with wound care companies such as Coloplast, Convatec, Essity, Mölnlycke, Solventum, and MiMedx to support EscharEx clinical programs and integrate leading compression and dressing technologies into trial designs.

Government and Institutional Support

Development of NexoBrid has been supported with federal funds from the U.S. Biomedical Advanced Research and Development Authority (BARDA) under a multi‑year contract. Company disclosures state that BARDA funding has contributed to pivotal clinical studies, pediatric trials, regulatory submissions, procurement for emergency preparedness, and health economic analyses. Additional funding from the U.S. Department of Defense has been directed toward development of a room temperature‑stable formulation of NexoBrid and related manufacturing and clinical preparations.

Financial and Corporate Profile

MediWound reports its financial results under International Financial Reporting Standards and files periodic reports with the U.S. Securities and Exchange Commission as a foreign private issuer. Recent company updates describe revenue from product sales and development services, equity financings to support clinical and manufacturing initiatives, and cash and short‑term deposit balances. The company has used registered direct offerings under an effective shelf registration statement on Form F‑3 to raise capital for EscharEx pre‑commercial activities, manufacturing expansion, and general corporate purposes.

Business Model and Sector Classification

Based on its disclosures, MediWound operates as a biotechnology company within the medicinal and biological manufacturing space, focusing on enzymatic biologic therapies for tissue repair. Its business model combines in‑house development and manufacturing of biologic products with a mix of direct and partnered commercialization, particularly through regional and indication‑specific collaborations. The company is part of the broader manufacturing sector, with a specific emphasis on medicinal and botanical‑related biologic products.

FAQs about MediWound Ltd. (MDWD)

• What does MediWound Ltd. do?
  MediWound Ltd. is a global biotechnology company that develops, manufactures, and commercializes enzymatic, non‑surgical therapies for tissue repair. Its activities focus on enzymatic removal of eschar in thermal burns and debridement of chronic wounds.
• What is NexoBrid®?
  NexoBrid is a topically administered, FDA‑approved biological orphan drug indicated for the enzymatic removal of eschar in patients with deep partial‑ and full‑thickness thermal burns. It selectively removes non‑viable tissue while preserving viable tissue and is approved in over 40 countries, including the U.S., EU, and Japan.
• Where is NexoBrid marketed?
  Company disclosures state that NexoBrid is marketed in the United States, European Union, Japan, Australia, and other international markets through MediWound and its commercial partners.
• What is EscharEx®?
  EscharEx is a late‑stage investigational enzymatic therapy being developed for the debridement of chronic wounds. It is currently being evaluated in the global VALUE Phase III trial in venous leg ulcers and is planned for additional studies in other chronic wound indications.
• Is EscharEx approved for commercial use?
  No. EscharEx is described by the company as an investigational therapy in late‑stage clinical development and has not been characterized in the provided materials as an approved product.
• How is MediWound expanding its manufacturing capacity?
  MediWound reports that it has completed commissioning and expansion of a GMP manufacturing facility in Yavne, Israel, designed to increase NexoBrid production capacity approximately sixfold, with commercial availability subject to regulatory reviews.
• What role does BARDA play in MediWound’s business?
  The U.S. Biomedical Advanced Research and Development Authority (BARDA) has provided funding and technical support for NexoBrid’s pivotal clinical studies, pediatric trials, regulatory submissions, procurement for emergency preparedness, and additional projects such as health economic modeling and evaluation in mass‑casualty scenarios.
• On which exchange does MediWound trade and under what symbol?
  MediWound Ltd. trades on Nasdaq under the ticker symbol MDWD, as noted in company press releases and SEC filings.
• What industry and sector is MediWound classified in?
  The company is classified in medicinal and botanical manufacturing within the broader manufacturing sector, with a focus on biotechnology and biologic therapies for tissue repair.
• Does MediWound collaborate with other companies?
  Yes. MediWound reports collaborations with multiple global wound care companies, including Coloplast, Convatec, Essity, Mölnlycke, Solventum, and MiMedx, to support the EscharEx clinical program and integrate complementary wound care products into its trials.