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MediWound to Participate in the BTIG Virtual MedTech, Digital Health, Life Science & Diagnostic Tools Conference

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MediWound Ltd. (Nasdaq: MDWD) announced that CEO Sharon Malka will participate in a fireside chat at the BTIG Virtual MedTech, Digital Health, Life Science & Diagnostic Tools Conference on February 18, 2021, at 11:30 am ET. The event will be live-streamed on the company's website. MediWound specializes in innovative therapies for severe burn and wound management, notably its products NexoBrid and EscharEx, which utilize patented proteolytic enzyme technology. NexoBrid has received multiple market authorizations, including from the European Medicines Agency.

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YAVNE, Israel, Feb. 10, 2021 (GLOBE NEWSWIRE) -- MediWound Ltd. (Nasdaq: MDWD), a fully-integrated biopharmaceutical company bringing innovative therapies to address unmet needs in severe burn and wound management, today announced that Sharon Malka, Chief Executive Officer, will participate in a fireside chat during the BTIG Virtual MedTech, Digital Health, Life Science & Diagnostic Tools Conference, which is being held February 17-19, 2021.

Event Details
Date:Thursday, February 18
Time:11:30 am ET

A live webcast of the fireside chat will be available on Events page of the Investors section of the company's website: www.mediwound.com.

About MediWound Ltd.
MediWound is a fully-integrated biopharmaceutical company focused on developing, manufacturing and commercializing novel therapeutics based on its patented proteolytic enzyme technology to address unmet needs in the fields of severe burns, chronic and other hard-to-heal wounds. MediWound’s first innovative biopharmaceutical product, NexoBrid®, non-surgically and rapidly removes burn eschar without harming viable tissue. The product has received marketing authorization from the European Medicines Agency as well as the Israeli, Argentinian, South Korean, Russian and Peruvian Ministries of Health for eschar removal (debridement) in adults with deep partial-thickness and/or full-thickness thermal burns. On June 29, 2020, a biological license application (BLA) was submitted to the U.S. FDA and was assigned a Prescription Drug User Fee Act (PDUFA) target date of June 29, 2021. MediWound’s second innovative product, EscharEx is a topical biological drug candidate for the debridement of chronic and other hard-to-heal wounds using the same proteolytic enzyme technology as NexoBrid. In two Phase 2 studies, EscharEx® has demonstrated safety and efficacy in the debridement of various chronic and other hard-to-heal wounds, within a few daily applications. EscharEx active substance (API) is a concentrate of proteolytic enzymes enriched in bromelain. EscharEx is an investigational product, currently under a U.S. phase 2 adaptive design study. For more information, please visit www.mediwound.com.

Contacts: 
Boaz Gur-Lavie Jeremy Feffer
Chief Financial Officer Managing Director, LifeSci Advisors
MediWound Ltd. 212-915-2568
ir@mediwound.comjeremy@lifesciadvisors.com


FAQ

When is MediWound's CEO participating in the BTIG Conference?

MediWound's CEO, Sharon Malka, will participate in the BTIG Conference on February 18, 2021, at 11:30 am ET.

Where can I watch the MediWound CEO's fireside chat?

The fireside chat can be watched live on MediWound's website under the Investors section.

What products does MediWound focus on?

MediWound focuses on innovative therapies for severe burns and hard-to-heal wounds, particularly NexoBrid and EscharEx.

What is NexoBrid used for?

NexoBrid is used for non-surgical removal of burn eschar without harming healthy tissue.

What is the status of EscharEx?

EscharEx is currently an investigational product in a U.S. phase 2 adaptive design study.

MediWound Ltd.

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