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Drug

Sugammadex

Approved · FDA / EMA
Emerging researchLate-stage developmentRising momentum

Also known as Bridion.

24
Research papers
11
Active clinical trials
9
Regulatory events
Latest activity
beta

Recent clinical, regulatory, research and industry developments relating to this drug.

Approval: SUGAMMADEX (ANDA213915)

Regulatory2026-07-28FDA

Approval: SUGAMMADEX (ANDA214236)

Regulatory2026-07-28FDA

Approval: SUGAMMADEX (ANDA214311)

Regulatory2026-07-28FDA

Approval: SUGAMMADEX (ANDA214319)

Regulatory2026-07-28FDA

Profile

Identifiers & mechanism

Canonical identifiers, marketed brand names and mechanism, resolved across RxNorm, ChEMBL and ATC.

Canonical name
Sugammadex
Aliases & brands
Bridion
RxNorm CUI
1726988
ChEMBL ID
CHEMBL5412674
UNII
361LPM2T56
Regulatory jurisdictions
emafda

Regulatory timeline

9 events

The complete regulatory record, grouped by authority — approvals, safety advisories and label changes. Each authority shows its most recent events; expand one to read its full history.

Earliest approval
2008-07-25
Latest approval
2026-07-28
Authorities
FDA · EMA
Total events
9
fdaU.S. Food and Drug Administration· 8 events
2026-07-28Approval
Approval: SUGAMMADEX (ANDA215260)
Evidence ↗
2026-07-28Approval
Approval: SUGAMMADEX (ANDA214236)
Evidence ↗
2026-07-28Approval
Approval: SUGAMMADEX (ANDA214311)
Evidence ↗
emaEuropean Medicines Agency· 1 event
2008-07-25Approval
Approval: Bridion (EMA)
Indication: Reversal of neuromuscular blockade induced by rocuronium or vecuronium. For the peadiatric population: sugammadex is only recommended for routine reversal of rocuronium-inducedShow full indication

Reversal of neuromuscular blockade induced by rocuronium or vecuronium. For the peadiatric population: sugammadex is only recommended for routine reversal of rocuronium-induced blockade in children and adolescents.

Evidence ↗

Data from the U.S. Food and Drug Administration (U.S. Food and Drug Administration), public domain (CC0).

Contains information from the European Medicines Agency (European Medicines Agency), © EMA, reused under CC BY 4.0.

Clinical trials

170 trials

The current development programme across all trial phases — status mix, phase distribution and the late-stage studies shaping the evidence base.

Development programme
CLINICALTRIALS.GOV · LIVE REGISTRY
170
registered trials across all phases
LATEST COMPLETION 2026
11
Active studies
11
Recruiting
154
Late-stage (III+)
122
Completed
37
Discontinued
PHASE DISTRIBUTIONn = 170
Early Phase 11Phase 14Phase 1 / 21Phase 210Phase 2 / 33Phase 331Phase 485Phase N / A35

Late-stage studies

Phase III+ trials still open or recently active — where late-stage evidence is being generated.

Recent completions

Trials that read out recently, adding to the completed evidence base.

Research activity

24 papers

Key research shaping understanding of this drug, combining the latest publications with the most influential evidence.

Publications over time
20082022
Most influential
Recent papers
Major research themes8
Neuromuscular Blockade7Neuromuscular Nondepolarizing Agents4gamma-Cyclodextrins3Androstanols1Anesthesia Recovery Period1Anesthesia, General1Anesthetics1Blood Loss, Surgical1
Journals, researchers & institutions
Top journals
  • British journal of anaesthesia6
  • Anesthesiology4
  • Anesthesia and analgesia2
  • BMC anesthesiology2
  • European journal of anaesthesiology2
  • American journal of therapeutics1
Leading researchers
  • Woo T6
  • Rietbergen H5
  • Blobner M2
  • de Bie J2
  • Demeyer I2
  • Gutstein DE2
  • Jahr JS2
  • Khuenl-Brady KS2
Leading institutions
free-text, unnormalised
  • Academic Teaching Hospital1
  • Accurate Clinical Trials/Saddleback Memorial Medical Center1
  • Asan Medical Center1
  • Asker and Baerum Hospital1
  • Beijing Chaoyang Hospital1
  • Canisius-Wilhelmina Hospital1

Related drugs

1 matches

Drugs sharing diseases, protein targets and literature with this one. Ranked by graph evidence (shared targets + diseases weighted above co-mentions).

Frequently co-studied with Sugammadex in the research literature.

2 shared papers
References & data sources
  • RxNorm (U.S. National Library of Medicine) — drug identity
  • ChEMBL (EMBL-EBI) & UniProt — pharmacology and targets
  • Europe PMC — research literature
  • ClinicalTrials.gov — clinical trials
  • Regulatory event sources are credited in the Regulatory Timeline above.