Drug intelligence / Profile preview

Sugammadex

Development stage
Approved
Lead developer
Organon
Modality
Small Molecules, Biodegradable Polymers → Polymer-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Intravenous
01

Overview

Sugammadex is a modified gamma-cyclodextrin and the first selective relaxant binding agent, used to reverse neuromuscular blockade induced by the aminosteroidal nondepolarizing neuromuscular blocking agents rocuronium and vecuronium during general anesthesia. It works by encapsulating these steroidal neuromuscular blocking drugs in plasma, forming tight 1:1 water-soluble complexes that prevent their action at the neuromuscular junction. This creates a concentration gradient that draws the muscle relaxant away from its site of action, rapidly reversing paralysis. Sugammadex does not inhibit acetylcholinesterase and therefore avoids cholinergic side effects associated with traditional reversal agents like neostigmine. It is administered intravenously at the end of surgery to restore muscle function. Developed by Organon and manufactured by Merck Sharp and Dohme.

Brand names
Bridion
Other names
sugammadex sodiummodified gamma-cyclodextrin
02

Targets

Muscle-type nicotinic acetylcholine receptor

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