Sugammadex

drug
On this page

Summary

Sugammadex (CHEMBL2111107) is an approved oligosaccharide (ATC V03AB35); indicated across 9 conditions including burn and morbid obesity.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Oligosaccharide
  • ATC class: V03AB35
  • Indications: 9 conditions
  • Clinical trials: 208
  • Chemistry: 2002.2 Da · C72H112O48S8

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2111107
NameSugammadex
TypeOligosaccharide
Max phase4
FDA approvedno
PubChem CID70693550
ATCV03AB35
Molecular formulaC72H112O48S8
Molecular weight2002.2
InChIKeyWHRODDIHRRDWEW-ZWYCLXBASA-N

SMILES: C(CSC[C@@H]1[C@@H]2[C@@H]([C@H]([C@H](O1)O[C@@H]3[C@H](O[C@@H]([C@@H]([C@H]3O)O)O[C@@H]4[C@H](O[C@@H]([C@@H]([C@H]4O)O)O[C@@H]5[C@H](O[C@@H]([C@@H]([C@H]5O)O)O[C@@H]6[C@H](O[C@@H](C([C@H]6O)O)O[C@@H]7[C@H](O[C@@H]([C@@H]([C@H]7O)O)O[C@@H]8[C@H](O[C@@H]([C@@H]([C@H]8O)O)O[C@@H]9[C@H](O[C@H](O2)[C@@H]([C@H]9O)O)CSCCC(=O)O)CSCCC(=O)O)CSCCC(=O)O)CSCCC(=O)O)CSCCC(=O)O)CSCCC(=O)O)CSCCC(=O)O)O)O)C(=O)O

IUPAC name: 3-[[(1S,3S,5S,6S,8S,10S,11S,13S,15S,16S,18S,20S,21S,23S,25S,26S,28S,30S,31S,33S,35S,36S,38S,40S,41R,43R,44R,45R,46R,47R,48R,49R,50R,51R,52R,53R,54R,55R,56R)-10,15,20,25,30,35,40-heptakis(2-carboxyethylsulfanylmethyl)-41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56-hexadecahydroxy-2,4,7,9,12,14,17,19,22,24,27,29,32,34,37,39-hexadecaoxanonacyclo[36.2.2.23,6.28,11.213,16.218,21.223,26.228,31.233,36]hexapentacontan-5-yl]methylsulfanyl]propanoic acid

Also known as: Sugammadex, SUGAMMADEX

Parent form; salt/anhydrous children: CHEMBL2107374

Patent coverage: 17 distinct patent families (22 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

9 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
burn3MONDO:0043519EFO:0009516
morbid obesity2MONDO:0005139EFO:0001074
obesity disorder2MONDO:0011122EFO:0001073
kidney disorder2MONDO:0005240EFO:0003086
allergic disease1MONDO:0005271MONDO:0005271

4 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 208.

Phase distribution

PhaseTrials
PHASE494
Not specified54
PHASE334
PHASE214
PHASE16
PHASE2/PHASE33
PHASE1/PHASE22
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06112353PHASE4RECRUITINGNeuromuscular Blockade Comparison for GI-2 Recovery After Bowel Resection
NCT07203287PHASE4RECRUITINGRisk of Acute Complications With Rocuronium vs Cisatracurium in Patients With Chronic Kidney Disease
NCT07477132PHASE4NOT_YET_RECRUITINGA Dose-response Study to Determine the Right Dosage of Sugammadex as a Reversal Agent of Rocuronium in Infants Between 1 and 24 Months Old
NCT00895609PHASE4COMPLETEDSugammadex and Neostigmine at Shallow Neuromuscular Blockade
NCT01101139PHASE4COMPLETEDSugammadex Improves Muscle Function After Standard Neuromuscular Recovery
NCT01142648PHASE4COMPLETEDSugammadex and Brain Waves
NCT01424488PHASE4UNKNOWNSugammadex Efficacy and Safety for Reversal of Pipecuronium-induced Neuromuscular Blockade
NCT01453530PHASE4UNKNOWNStreet Fitness in Surgical Patients Undergoing General Anesthesia After Reversal of Neuromuscular Blockade
NCT01539044PHASE4COMPLETEDOptimal Relaxation Technique for Laparotomies With Rocuronium Infusion Followed by Sugammadex Reversal
NCT01579851PHASE4COMPLETEDRecovery After Sugammadex(Propofol vs Sevoflurane)
NCT01718236PHASE4COMPLETEDModern Myorelaxation Procedure and Reversal of Neuromuscular Blockade With General Anesthesia for Caesarean Section
NCT01728584PHASE4COMPLETEDA Study Comparing the Use of Deep or Standard Neuromuscular Blockade in Combination With Low or Standard Insufflation Pressures in Participants Undergoing Laparoscopic Cholecystectomy (P07982)
NCT01761552PHASE4UNKNOWNA Prospective, Randomized Controlled Trial Comparing Traditional Methods of Neuromuscular Block Reversal to Sugammadex for Extubation in the Operating Room in ASA 4 and 4E Patients
NCT01785758PHASE4COMPLETEDEfficacy and Safety of Sugammadex in Renal Diseased Patients
NCT01933425PHASE4COMPLETEDOptimizing Surgical Conditions During Gynecologic Laparoscopic Surgery With Deep Neuromuscular Blockade
NCT01965067PHASE4COMPLETEDInfluence of Mild Hypothermia on Reversal of Rocuronium With Sugammadex
NCT01972659PHASE4COMPLETEDEffects of Magnesium Sulphate on Sugammadex Reversal of Rocuronium Induced Blockade in Gynaecology Patients
NCT02079337PHASE4COMPLETEDValidation of Subjective Rating Scales Used to Assess Surgical Conditions in Abdominal Surgery
NCT02160223PHASE4COMPLETEDSugammadex Compared With Neostigmin/Atropin for Neuromuscular Block Reversal in Patients With Obstructive Sleep Apnea
NCT02215382PHASE4COMPLETEDIntraocular Pressure Changes Associated With Tracheal Extubation: Comparison of Sugammadex With Conventional Reversal of Neuromuscular Blockade
NCT02243943PHASE4COMPLETEDEffect of Neuromuscular Reversal With Sugammadex on Postoperative Recovery Profile
NCT02247466PHASE4COMPLETEDOptimizing Surgical Conditions During Laparoscopic Herniotomy With Deep Neuromuscular Blockade
NCT02256280PHASE4TERMINATEDA Randomized Double Blind Controlled Trial Comparing Sugammadex and Neostigmine After Thoracic Anesthesia
NCT02284412PHASE4COMPLETEDFunctional Respiratory Imaging After Neostigmine or Sugammadex
NCT02286752PHASE4COMPLETEDComparison of the Effects of Neostigmine With Sugammadex on Postoperative Nausea and Vomiting.
NCT02329964PHASE4UNKNOWNEffectiveness of Sugammadex in LMS Surgery
NCT02361060PHASE4COMPLETEDEffects of Neuromuscular Block Reversal With Sugammadex vs Neostigmine on Postoperative Respiratory Outcomes After Major Abdominal Surgery
NCT02375217PHASE4COMPLETEDLow Dose Sugammadex Combined With Neostigmine and Glycopyrrolate Versus Full Dose Sugammadex for Reversal of Rocuronium-induced Neuromuscular Blockade: a Cost Saving Strategy
NCT02390817PHASE4COMPLETEDEffect of Sugammadex for Muscle Motor Response and Awareness in Intraoperative Wakeup
NCT02403063PHASE4COMPLETEDElectromyographic Activity of the Respiratory Muscles During Neostigmine or Sugammadex Enhanced Recovery After Neuromuscular Blockade
NCT02410590PHASE4WITHDRAWNRocuronium + Sugammadex vs. Succinylcholine + Cisatracurium + Neostigmine/Atropine in Obese Participants (MK-8616-104)
NCT02414880PHASE4COMPLETEDSugammadex Versus Neostigmine in Patients With Liver Cirrhosis Undergoing Liver Resection
NCT02451202PHASE4COMPLETEDDeep vs Moderate Neuromuscular Blockade With Rocuronium in Patients Undergoing Endolaryngeal Procedures
NCT02455921PHASE4COMPLETEDNeuromuscular Blockade Reversal Agent Effect on Postoperative Cognitive Function and Behaviour in Children
NCT02484651PHASE4COMPLETEDCan Adequacy of Anesthesia Depth and Quality of Recovery be Influenced by the Level of Neuromuscular Blockade?
NCT02568345PHASE4COMPLETEDSugammadex ED90 Dose in the Obese Patients
NCT02580188PHASE4COMPLETEDThe Effect of Deep Neuromuscular Block on Surgical Condition During Laparoscopic Colorectal Surgery
NCT02698969PHASE4UNKNOWNRecovery of Muscle Function After Deep Neuromuscular Block by Means of Diaphragm Ultrasonography
NCT02708056PHASE4COMPLETEDSugammadex Given for the Reversal of Rocuronium Induced Neuromuscular Blockade Under Sevoflurane Anesthesia in Infants
NCT02724111PHASE4COMPLETEDEffect of Neuromuscular Blockade on Operating Conditions and Overall Satisfaction During Spinal Surgery

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).