Praziquantel

drug
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Also known as BiltricideCesolCisticidCysticideCestocurEMBAY 8440EMBAY-8440NSC-757285PrazicuantelPraziquantel component of broadlinePraziquantel component of profenderPraziquantelumSID26747203SID50105220SID855582SID858012SID90341571SID85231186SID144209148

Summary

Praziquantel (CHEMBL976) is an approved small molecule (ATC P02BA01); indicated across 7 conditions including schistosomiasis and helminthiasis.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: P02BA01
  • Indications: 7 conditions
  • Clinical trials: 37
  • Chemistry: 312.4 Da · C19H24N2O2

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL976
NamePraziquantel
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID4891
ATCP02BA01
Molecular formulaC19H24N2O2
Molecular weight312.4
InChIKeyFSVJFNAIGNNGKK-UHFFFAOYSA-N

SMILES: C1CCC(CC1)C(=O)N2CC3C4=CC=CC=C4CCN3C(=O)C2

IUPAC name: 2-(cyclohexanecarbonyl)-3,6,7,11b-tetrahydro-1H-pyrazino[2,1-a]isoquinolin-4-one

Also known as: Biltricide, Cesol, Cisticid, Cysticide, Cestocur, EMBAY 8440, EMBAY-8440, NSC-757285, Prazicuantel, Praziquantel, Praziquantel component of broadline, Praziquantel component of profender

Patent coverage: 4,086 distinct patent families (13,070 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 12,899 (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

Broader ChEMBL bioactivity targets: 11 (assay-derived). Sample: Survival motor neuron protein, Prelamin-A/C, RecQ-like DNA helicase BLM, Kappa-type opioid receptor, Muscarinic acetylcholine receptor M1, Cytochrome P450 3A4, Aldehyde dehydrogenase 1A1, Mitogen-activated protein kinase 1, Cellular tumor antigen p53, Neuropeptide S receptor, Bile salt export pump.

Bioactivity

ChEMBL activities: 5 potent at pChembl ≥ 5 of 18 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
BLM8.49Potency3.2nMCHEMBL_ACT_4746015
BLM8.49Potency3.2nMCHEMBL_ACT_4929720
TP536.9Potency125.9nMCHEMBL_ACT_4874103
SMN15.85Potency1412nMCHEMBL_ACT_3889455
NPSR15.2Potency6310nMCHEMBL_ACT_4940733

Target pathways

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

Indications & clinical

Indications

3 approved indications. FDA phase 4, plus an anticancer drug’s labelled cancer uses (which ChEMBL often logs at phase 3).

IndicationPhaseMONDOEFO
schistosomiasis4MONDO:0015254EFO:1001475
helminthiasis4MONDO:0004664EFO:1001342
opisthorchiasis4MONDO:0005884EFO:0007404

3 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.

Disease (in trials)PhaseMONDOEFO
cysticercosis3MONDO:0015484EFO:0007231
urinary schistosomiasis3MONDO:0006001EFO:0007530
Schistosoma mansoni infectious disease2MONDO:0044345MONDO:0008412

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

Clinical trials

Total trials: 37.

Phase distribution

PhaseTrials
Not specified15
PHASE36
PHASE45
PHASE15
PHASE2/PHASE33
PHASE23

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06376396PHASE4NOT_YET_RECRUITINGAssessment of Combined Praziquantel and Albendazole vs Albendazole Alone to Treat Active Parenchymal Neurocysticercosis
NCT07074444PHASE4RECRUITINGTreatment of Clonorchiasis in Guangxi With Albendazole, Tribendimidine, and Praziquantel
NCT00403611PHASE4COMPLETEDEvaluation of Praziquantel Dosage for Treatment of Schistosomiasis in Brazil
NCT02734186PHASE4WITHDRAWNEffect of Concomitant Mansonella Perstans Microfilaremia on Immune Responses Following Single Dose Praziquantel in People With Schistosomiasis
NCT02878564PHASE4COMPLETEDEffect of Schistosomiasis Mansoni on HIV Susceptibility and Female Genital Immunology
NCT00441285PHASE2/PHASE3COMPLETEDNeurocysticercosis: Combined Treatment With Praziquantel (PZQ) and Albendazole (ABZ)
NCT00510159PHASE2/PHASE3COMPLETEDComparing Praziquantel Versus Artesunate + Sulfamethoxypyrazine/Pyrimethamine for Treating Schistosomiasis
NCT01054651PHASE3COMPLETEDA Randomised Trial of Artesunate-sulfamethoxypyrazine/Pyrimethamine Versus Praziquantel for the Treatment of S. Mansoni
NCT01558336PHASE3COMPLETEDSchistosoma Haematobium Infections and Praziquantel
NCT01722539PHASE3COMPLETEDImpact IPT With Sulfadoxine-pyrimethamine or Sulfadoxine-pyrimethamine Plus Piperaquine in Schoolchildren
NCT02947581PHASE3TERMINATEDSub Arachnoid Neurocysticercosis Treatment Outcome (SANTO)
NCT03779347PHASE3UNKNOWNSchistosomiasis Diagnosis Using a CAA Antigen Test
NCT03893097PHASE3COMPLETEDEvaluation of Artesunate-mefloquine as a Novel Alternative Treatment for Schistosomiasis in African Children
NCT04679831PHASE2/PHASE3COMPLETEDClinical Evaluation of Ujiplus® Against Schistosoma Mansoni
NCT00486863PHASE2COMPLETEDS. Japonicum and Pregnancy Outcomes
NCT01901484PHASE2COMPLETEDSchistosoma Mansoni Morbidity in Children Aged 1-5 Years
NCT03640377PHASE2COMPLETEDPraziquantel in Children Under Age 4
NCT01288872PHASE1COMPLETEDPraziquantel-Pharmacokinetic Study
NCT02271984PHASE1COMPLETEDRelative Bioavailability Trial of L-Praziquantel in Healthy Volunteers
NCT02325713PHASE1COMPLETEDRelative Bioavailability Trial of Oral Dispersible Praziquantel Tablets in Healthy Volunteers
NCT03437447PHASE1COMPLETEDPraziquantel Bioequivalence Study
NCT04314037PHASE1COMPLETEDBioequivalence Study of Coated Cesol Tablet Formulation Versus Biltricide
NCT00215267Not specifiedCOMPLETEDThe Effect of Praziquantel Treatment on Schistosoma Mansoni Morbidity and re-Infection Along Lake Victoria, Uganda
NCT00231322Not specifiedCOMPLETEDInfluence of Transmission Season on Outcome of Treatment of Schistosoma Haematobium Infection in Mozambique
NCT00347113Not specifiedCOMPLETEDSchistosome and Intestinal Worm Infections and Malaria Morbidity Among School and Pre-school Children in, Tanzania
NCT00507221Not specifiedCOMPLETEDEmpiric Therapy of Helminth Co-infection to Reduce HIV-1 Disease Progression
NCT00817713Not specifiedTERMINATEDCan Presumptive Anthelminthic Treatment Delay the Progression of HIV in ART-naïve Patients in Rural Africa?
NCT01050374Not specifiedCOMPLETEDSafety and Efficacy of Drug Combinations Against Schistosomiasis
NCT01050517Not specifiedCOMPLETEDSafety and Efficacy of Drug Combinations Against Triple Infections
NCT01154907Not specifiedUNKNOWNPrevention of Female Genital Schistosomiasis (FGS) in Rural High-endemic South Africa
NCT01260012Not specifiedUNKNOWNAntioxidant Supplements in the Reversal of Schistosomal Peri-portal Fibrosis
NCT01541631Not specifiedUNKNOWNA Study of Co-infections of HIV-1 and Schistosoma Mansoni and Its Impact on Praziquantel Treatment Outcomes
NCT02144389Not specifiedCOMPLETEDArachidonic Acid Treatment Against Schistosomiasis Infection in Children
NCT02162875Not specifiedCOMPLETEDSchistosoma Mansoni in Mwanza Region, Tanzania
NCT02612896Not specifiedCOMPLETEDTaenia Solium Elimination Versus Control: What is the Best Way Forward for Sub-Saharan Africa?
NCT04635553Not specifiedUNKNOWNMonitoring Schistosome Hybrids Under Under Praziquantel Pressure
NCT05354258Not specifiedUNKNOWNFeasibility and Safety of Combining Anti-malarial With Deworming Drugs in African Children

Clinical evidence (CIViC)

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

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline, but PharmGKB curates 0 clinical and 6 variant annotation(s) for this drug (gene-keyed; see PharmGKB).

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