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NEXOBRID (Nexo Pharmaceuticals Pty Ltd)

Product name
NEXOBRID
Date registered
Evaluation commenced
Decision date
Approval time
208 (255 working days)
Active ingredients
anacaulase-bcdb
Registration type
NCE/ NBE
Indication

The approved indications for this therapeutic good are:

  • NEXOBRID is indicated for eschar removal in adults and paediatric patients with deep partial thickness (DPT) and/or full thickness (FT) thermal burns.
  • For further information on acceptable burn types, see Section 4.4 Special Warnings and Precautions.

Registration process

Orphan drug
Sponsors receive a fee waiver to help bring medicines for a small population to market.