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NEXOBRID (ANACAULASE-BCDB)

MEDIWOUND, LTD · FDA-approved approved ✓ Verified May 2026

NEXOBRID (generic name: ANACAULASE-BCDB) is a drug developed by MEDIWOUND, LTD. It is currently FDA-approved for Removal of escars from deep thermal burn.

NexoBrid is an enzyme-based treatment used for the removal of necrotic tissue. It is being studied for the treatment of acute deep partial and full thickness burn injuries.

At a glance

Generic nameANACAULASE-BCDB
SponsorMEDIWOUND, LTD
Therapeutic areaOther
PhaseFDA-approved

Approved indications

Common side effects

Serious adverse events

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about NEXOBRID

What is NEXOBRID?

NEXOBRID (ANACAULASE-BCDB) is a pharmaceutical drug developed by MEDIWOUND, LTD, indicated for Removal of escars from deep thermal burn.

What is NEXOBRID used for?

NEXOBRID is indicated for Removal of escars from deep thermal burn.

Who makes NEXOBRID?

NEXOBRID is developed and marketed by MEDIWOUND, LTD (see full MEDIWOUND, LTD pipeline at /company/mediwound-ltd).

What is the generic name of NEXOBRID?

ANACAULASE-BCDB is the generic (nonproprietary) name of NEXOBRID.

What development phase is NEXOBRID in?

NEXOBRID is FDA-approved (marketed).

What are the side effects of NEXOBRID?

Common side effects of NEXOBRID include Pruritus, Pyrexia. Serious adverse events: Anaphylaxis, Hypersensitivity, Urticaria.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing