Ramosetron

drug
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Also known as SID50112691Ramosetron (Hydrochloride)

Summary

Ramosetron (CHEMBL1643895) is an approved small molecule; indicated across 7 conditions including gastric neoplasm and neoplasm.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • Indications: 7 conditions
  • Clinical trials: 42
  • Chemistry: 279.34 Da · C17H17N3O

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1643895
NameRamosetron
TypeSmall molecule
Max phase4
FDA approvedno
PubChem CID108000
Molecular formulaC17H17N3O
Molecular weight279.34
InChIKeyNTHPAPBPFQJABD-LLVKDONJSA-N

SMILES: CN1C=C(C2=CC=CC=C21)C(=O)[C@@H]3CCC4=C(C3)NC=N4

IUPAC name: (1-methylindol-3-yl)-[(5R)-4,5,6,7-tetrahydro-3H-benzimidazol-5-yl]methanone

Also known as: Ramosetron, SID50112691, RAMOSETRON, ramosetron, Ramosetron (Hydrochloride)

Parent form; salt/anhydrous children: CHEMBL3181841

Patent coverage: 2,534 distinct patent families (10,859 SureChEMBL compound mentions), from 3 matched compound structure(s). One matched structure accounts for 10,766 (99%) 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

Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).

GeneTargetActionpAffinityCancer dependencyUniProt
5-HT3AAntagonist10

Broader ChEMBL bioactivity targets: 9 (assay-derived). Sample: 5-hydroxytryptamine receptor 2B, Alpha-2A adrenergic receptor, 5-hydroxytryptamine receptor 3A, Alpha-2C adrenergic receptor, Alpha-2B adrenergic receptor, Sodium-dependent serotonin transporter, Kappa-type opioid receptor, Voltage-gated inwardly rectifying potassium channel KCNH2, Gamma-aminobutyric acid receptor subunit alpha-1.

Bioactivity

ChEMBL activities: 7 potent at pChembl ≥ 5 of 11 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
HTR3A10.22Ki0.06nMCHEMBL_ACT_17684870
HTR3A10.22Ki0.06nMCHEMBL_ACT_5125664
HTR3A9.4AC500.4nMCHEMBL_ACT_25149342
ADRA2B6.47AC50340nMCHEMBL_ACT_25143920
SLC6A45.41AC503900nMCHEMBL_ACT_25150548
ADRA2A5.37AC504300nMCHEMBL_ACT_25220100
KCNH25.33AC504700nMCHEMBL_ACT_25118175

Target pathways

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

Indications & clinical

Indications

7 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
gastric neoplasm3MONDO:0021085MONDO:0001056
neoplasm3MONDO:0005070MONDO:0004992

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

Clinical trials

Total trials: 42.

Phase distribution

PhaseTrials
Not specified17
PHASE413
PHASE36
PHASE24
PHASE2/PHASE31
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07574320PHASE4NOT_YET_RECRUITINGEffect of Ramosetron in Patients With Diarrhea Predominant Irritable Bowel Syndrome
NCT00918411PHASE4COMPLETEDA Preliminary Study to Explore Clinical Endpoints in Patients (Male) With Diarrhea-predominant Irritable Bowel Syndrome
NCT01102491PHASE4COMPLETEDAdditional Anti-emetic Effect of Ramosetron Prophylaxis After Total Knee Arthroplasty
NCT01225237PHASE4COMPLETEDA Study to Evaluate Efficacy of Ramosetron on Diarrhea-predominant Irritable Bowel Syndrome (IBS) in Male Patients
NCT01427127PHASE4UNKNOWNEffect of Ramosetron on Bowel Motility After Colorectal Resection
NCT01637545PHASE4TERMINATEDEvaluation of Safety and Efficacy of Nasea(R)/Ramosetron Inj. in Patients Undergoing Facial Bone Fracture Operations
NCT02478645PHASE4COMPLETEDDose-ranging Study of Ramosetron for the Prevention of Nausea and Vomiting After Gynecologic Laparoscopic Surgery
NCT02480088PHASE4COMPLETEDComparison of Palonosetron and Ramosetron for Preventing Patient-controlled Analgesia Related Nausea and Vomiting Following Spine Surgery; Association With ABCB1 Polymorphism
NCT02532634PHASE4COMPLETEDRamosetron, Aprepitant, and Dexamethasone Versus Palonosetron, Aprepitant, and Dexamethasone
NCT02803788PHASE4UNKNOWNPost-operative Nausea Vomiting in Laparoscopic Cholecystectomy
NCT02849483PHASE4UNKNOWNEffect of Ramosetron on Bowel Motility After Gynecological Surgery
NCT03278522PHASE4COMPLETEDRamosetron Pre-treatment for PONV and QT Prolongation
NCT04297293PHASE4UNKNOWNRamosetron OD Tablet and Postdischarge Nausea and Vomiting
NCT00272285PHASE3COMPLETEDA Study of Ramosetron Plus DX, Dexamethasone, Compared to Granisetron Plus DX for the Prevention of Vomiting and Nausea
NCT00971399PHASE3COMPLETEDRamosetron Versus Ondansetron for Radiotherapy Induced Nausea and Vomiting
NCT01536691PHASE3UNKNOWNRamosetron, Aprepitant and Dexamethasone Versus Ondansetron, Aprepitant and Dexamethasone
NCT02011659PHASE3UNKNOWNLong Term Prevention of Nausea and Vomiting in Gynecologic Laparoscopy
NCT02444897PHASE3COMPLETEDThe Comparison Between Epidural and Intravenous Patient-controlled Analgesia for Laparoscopic Gastrectomy
NCT02830906PHASE3COMPLETEDEffect of Ramosetron in Prevention of Intrathecal Morphine Induced Nausea and Vomiting
NCT06166615PHASE2/PHASE3UNKNOWNThe Safety and Efficacy of 5-HT3 Receptor Antagonist (Ramosetron) for the Treatment of Fecal Incontinence
NCT01012336PHASE2COMPLETEDSafety and Efficacy of Aprepitant, Ramosetron, and Dexamethasone for Chemotherapy-Induced Nausea and Vomiting in Patients With Ovarian Cancer Treated With Taxane/Carboplatin
NCT01046461PHASE2UNKNOWNRamosetron, Aprepitant and Dexamethasone (RAD) in Solid Cancer
NCT01788605PHASE2UNKNOWNEfficacy Study of Ramosetron in the Setting of Hematopoietic Stem Cell Transplantation
NCT01806948PHASE2COMPLETEDEfficacy Study of Antiemetics to Reduce Postoperative Nausea and Vomiting
NCT02869984EARLY_PHASE1UNKNOWNClinical Trial Assessing 5-HT3 Receptor Antagonist (Ramosetron) for the Treatment of Anterior Resection Syndrome
NCT05577845Not specifiedRECRUITING5-HT3 Receptor Antagonist (Ramosetron) vs Loperamide for the Treatment of Low Anterior Resection Syndrome(RALARS)
NCT01041183Not specifiedUNKNOWNThe Effect of Oral and Intravenous Ramosetron During Laparoscopic Cholecystectomy
NCT01169805Not specifiedCOMPLETEDProphylactic Effects of Ondansetron, Ramosetron, and Palonosetron on Patient-Controlled Analgesia Related Nausea and Vomiting After Urologic Laparoscopic Surgery
NCT01476280Not specifiedCOMPLETEDPalonosetron Versus Ramosetron for the Prevention of Postoperative Nausea and Vomiting
NCT01669213Not specifiedUNKNOWNEffects of Different Kinds, Different Doses of 5-HT3 Receptor Antagonists on Prevention of Hypotension
NCT01825733Not specifiedCOMPLETEDComparison of Palonosetron and Ramosetron for Preventing Patient-controlled Analgesia Related Nausea and Vomiting Following Spine Surgery
NCT02076529Not specifiedCOMPLETEDPhamacokinetic and Pharmacodynamic Study of Ramosetron in Chemotherapy Induced Nasea and Vomiting
NCT02139241Not specifiedCOMPLETEDThe Efficacy and Safety of Ramosetron in Patients Undergoing Off Pump Coronary Artery Bypass Surgery
NCT02416115Not specifiedCOMPLETEDAnti Emetic Efficacy of Combination of Ramosetron and Premixture of Naloxone With Patient-controlled Analgesia
NCT02597907Not specifiedCOMPLETEDPostoperative Nausea and Vomiting: Ramosetron Plus Aprepitant vs Palonosetron Plus Aprepitant
NCT02604797Not specifiedUNKNOWNAnalgesia Effects of Nalbuphine vs Sulfentanil
NCT02612649Not specifiedCOMPLETEDSpecial Drug Use Surveillance of Irribow in Female Patients
NCT02617121Not specifiedUNKNOWNThe Effects of Gabapentin and Ramosetron on Postoperative Nausea and Vomiting in Laparoscopic Gynecological Surgery
NCT02625181Not specifiedCOMPLETEDReal-time Decision Support for Postoperative Nausea and Vomiting (PONV) Prophylaxis
NCT03017222Not specifiedCOMPLETEDTherapeutic Efficacy of Ramosetron for Treatment of Established PONV After Laparoscopic Surgery

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).