Oliceridine

drug
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Also known as OliceridinaOlinvykOlynvikTRV-130TRV130OLICERIDINE (HYDROCHLORIDE)

Summary

Oliceridine (CHEMBL2443262) is an approved small molecule (ATC N02AX07); indicated across 1 condition.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: N02AX07
  • Indications: 1 condition
  • Clinical trials: 24
  • Chemistry: 386.6 Da · C22H30N2O2S

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2443262
NameOliceridine
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID66553195
ATCN02AX07
Molecular formulaC22H30N2O2S
Molecular weight386.6
InChIKeyDMNOVGJWPASQDL-OAQYLSRUSA-N

SMILES: COC1=C(SC=C1)CNCC[C@]2(CCOC3(C2)CCCC3)C4=CC=CC=N4

IUPAC name: N-[(3-methoxythiophen-2-yl)methyl]-2-[(9R)-9-pyridin-2-yl-6-oxaspiro[4.5]decan-9-yl]ethanamine

Also known as: Oliceridina, Oliceridine, Olinvyk, Olynvik, TRV-130, TRV130, OLICERIDINE, OLICERIDINE (HYDROCHLORIDE), Oliceridine (hydrochloride)

Parent form; salt/anhydrous children: CHEMBL6068518

Patent coverage: 137 distinct patent families (343 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 282 (82%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 11 (assay-derived). Sample: Voltage-dependent L-type calcium channel subunit alpha-1C, Sodium channel protein type 5 subunit alpha, D(2) dopamine receptor, Mu-type opioid receptor, D(3) dopamine receptor, Delta-type opioid receptor, Kappa-type opioid receptor, Voltage-gated inwardly rectifying potassium channel KCNH2, Mu-type opioid receptor, Cytochrome P450 2D6.

Bioactivity

ChEMBL activities: 25 potent at pChembl ≥ 5 of 29 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
OPRM18.84Ki1.46nMCHEMBL_ACT_24399183
OPRM18.74EC501.8nMCHEMBL_ACT_24399069
P428668.62EC502.4nMCHEMBL_ACT_25621804
P428668.62EC502.4nMCHEMBL_ACT_25621805
OPRM18.52EC503nMCHEMBL_ACT_28505294
OPRM18.36Ki4.38nMCHEMBL_ACT_25621603
OPRM18.22Ki6nMCHEMBL_ACT_13515283
OPRM18.17EC506.7nMCHEMBL_ACT_24399186
OPRM18.1EC508nMCHEMBL_ACT_13515280
OPRM18.1EC507.94nMCHEMBL_ACT_13515427
OPRM17.92EC5012nMCHEMBL_ACT_24399207
OPRM17.57Ki27nMCHEMBL_ACT_28840151
P428667.49EC5032.36nMCHEMBL_ACT_25621843
P428667.49EC5032.5nMCHEMBL_ACT_25621844
OPRM17.3EC5050.12nMCHEMBL_ACT_13515356
P428667.23EC5058.88nMCHEMBL_ACT_25621757
P428667.23EC5058.5nMCHEMBL_ACT_25621758
OPRK15.85EC501400nMCHEMBL_ACT_13515299
OPRD15.55EC502800nMCHEMBL_ACT_13515297
CYP2D65.34IC504600nMCHEMBL_ACT_28505405
SCN5A5.33IC504700nMCHEMBL_ACT_13515287
KCNH25.26IC505500nMCHEMBL_ACT_24399166
KCNH25.26IC505500nMCHEMBL_ACT_28505546
KCNH25.21IC506200nMCHEMBL_ACT_13515289
DRD35.16Ki6860nMCHEMBL_ACT_25621696

Target pathways

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

Indications & clinical

Indications

1 indication (1 at ChEMBL trial phase 4).

The 1 indication record carries no mapped disease name (EFO/MeSH-only); none shown.

Clinical trials

Total trials: 24.

Phase distribution

PhaseTrials
Not specified8
PHASE47
PHASE33
PHASE23
PHASE13

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06411665PHASE4RECRUITINGEffect of Oliceridine Analgesia on Postoperative Nause and Vomiting
NCT07018375PHASE4NOT_YET_RECRUITINGThe Effect of Oliceridine Patient-Controlled Intravenous Analgesia on Postoperative Chronic Pain After Video-Assisted Thoracoscopic Lobectomy
NCT07026162PHASE4RECRUITINGOliceridine on Postoperative Nausea and Vomiting in Gynecological Laparoscopic Surgery
NCT04979247PHASE4COMPLETEDIntravenous Oliceridine and Opioid-related Complications
NCT05465226PHASE4COMPLETEDOliceridine in Patients With Acute Burn Injuries
NCT06458400PHASE4COMPLETEDTo Evaluate the Efficacy and Safety of Tegileridine and Oliceridine Injections in the Treatment of Postoperative Pain
NCT07306702PHASE4WITHDRAWNDexmedetomidine-Enhanced PCIA After Lobectomy in Nicotine-Dependent Patients
NCT02656875PHASE3COMPLETEDA Open-label Study to Evaluate the Safety of TRV130 in Patients With Acute Pain
NCT02815709PHASE3COMPLETEDStudy of Oliceridine (TRV130) for the Treatment of Moderate to Severe Acute Pain After Bunionectomy
NCT02820324PHASE3COMPLETEDStudy of Oliceridine (TRV130) for the Treatment of Moderate to Severe Acute Pain After Abdominoplasty
NCT02100748PHASE2COMPLETEDA Study of TRV130 for the Treatment of Pain After Bunionectomy
NCT02335294PHASE2COMPLETEDA Study of TRV130 for the Treatment of Pain After Abdominoplasty
NCT02520297PHASE2TERMINATEDA Pilot Study of TRV130 for the Treatment of Fracture Pain
NCT02083315PHASE1COMPLETEDPharmacokinetics and Pharmacodynamics of TRV130, Morphine, and Placebo in Healthy Subjects
NCT02169934PHASE1COMPLETEDA Study to Investigate the Metabolism and Excretion of [14C]-TRV130 in Healthy Male Subjects
NCT02344303PHASE1COMPLETEDStudy of the Effects of TRV130, at Therapeutic and Supra Therapeutic Doses, on QTc Intervals
NCT06668298Not specifiedNOT_YET_RECRUITINGClinical Study of G Protein Biased Μ - Opioid Receptor Agonist Oliceridine for Optimizing Postoperative Analgesia Under General Anesthesia
NCT06990893Not specifiedRECRUITINGComparison of the Analgesic Effect of Oliceridine Versus Morphine or Sufentanil for Postoperative Analgesia in Lumbar Surgeries: a Randomized Control Trial
NCT07097038Not specifiedNOT_YET_RECRUITINGAnalgesic Effect and Safety of Oliceridine and Oxycodone in Vitrectomy
NCT07112157Not specifiedNOT_YET_RECRUITINGEfficacy of Oxalidine and Sufentanil in Strabismus Correction
NCT07479446Not specifiedRECRUITINGOliceridine Versus Sufentanil for Postoperative Nausea in Cerebellopontine Angle Surgery
NCT07154979Not specifiedCOMPLETEDOliceridine Dose for Tracheal Intubation Hemodynamic Elevation: Up-and-Down Trial
NCT07187765Not specifiedCOMPLETEDRespiratory Safety of Oliceridine During Sedated Gastrointestinal Endoscopy
NCT07372209Not specifiedCOMPLETEDEffects and Safety of Oliceridine in Anesthesia Induction:A Randomised Controlled Trial

Clinical evidence (CIViC)

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

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.

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

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.