Praziquantel
FDA-approved product (tablet, oral), marketed as Biltricide, Praziquantel.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Helminthiasis
- Infection
- Opisthorchiasis
- Schistosomiasis
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Quinoline derivatives and related substances
- FDA pharmacologic class
- Anthelmintic FDA label ↗
- Anti-infective classification
- Classified as another kind of anti-infective (for example an antifungal, antiviral or antiparasitic medicine).WHO ATC P02BA01; FDA class Anthelmintic
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against MRSA, E. coli and M. tuberculosis. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA41.6% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli41.8% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae29.4% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis58.6% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
A model’s estimate of laboratory activity against each pathogen species. It is not clinical effectiveness.
Evidence
Clinical and experimental
Documented evidenceClinical
50+registered studies name this medicine, for any condition. The registry search keeps the first 50, so there may be more. See them below.
Experimental
No evidence found
No laboratory measurement against the four pathogens in the ChEMBL records loaded here.
Docking
Computational · nothing measuredAutoDock Vina, one experimentally solved protein per pathogen. This project’s screening target is -7.0 kcal/mol, its own mark rather than a universal cutoff. A docking score is a structural hypothesis, not proof of binding, and requires experimental validation.
Other medicines to investigate
AI prediction · nothing measuredOther repurposing candidates: approved medicines besides Praziquantel with AI-predicted activity ≥40% against the chosen pathogen, leaving out existing antimicrobials. They are computational candidates for further investigation, not alternatives and not recommendations.
Sorted by AI-predicted activity, high to low. The order is not a ranking of which medicine is better.
- Cetrorelix AcetateExisting use: Ovulation Inhibition, Positive regulation of ovulation63.2% AI-predicted activityagainst MRSA50+ registered studies
- HexachloropheneExisting use: Phenol and derivatives63.2% AI-predicted activityagainst MRSALab records exist3 registered studies
- LorlatinibExisting use: Cancer, Lymphoma, Neoplasm and 1 more63.1% AI-predicted activityagainst MRSA50+ registered studies
- Alectinib HydrochlorideExisting use: Cancer, Neoplasm, Non-small cell lung carcinoma63.0% AI-predicted activityagainst MRSA13 registered studies
- AlpelisibExisting use: Breast cancer, Breast carcinoma, Breast neoplasm and 2 more63.0% AI-predicted activityagainst MRSA50+ registered studies
- Histrelin AcetateExisting use: Neoplasm, Prostate adenocarcinoma, Prostate cancer62.9% AI-predicted activityagainst MRSA13 registered studies
- Degarelix AcetateExisting use: Prostate adenocarcinoma, Prostate cancer, Prostate carcinoma62.9% AI-predicted activityagainst MRSA50+ registered studies
- Lasmiditan SuccinateExisting use: Migraine disorder62.8% AI-predicted activityagainst MRSANo documented evidence found
- TacrolimusExisting use: Atopic eczema, Delayed Graft Function, Eczematoid dermatitis and 3 more62.5% AI-predicted activityagainst MRSA50+ registered studies
- Rezafungin AcetateExisting use: Candidemia, Candidiasis, Candidiasis, Invasive62.4% AI-predicted activityagainst MRSA5 registered studies
- AvapritinibExisting use: Cancer, Gastrointestinal stromal tumor, Neoplasm62.2% AI-predicted activityagainst MRSA30 registered studies
- Ceruletide DiethylamineExisting use: Tests for bile duct patency62.2% AI-predicted activityagainst MRSANo documented evidence found
Registered studies
A registration describes a study; it does not establish a positive result.
Repeated Doses of Praziquantel in Schistosomiasis Treatment (RePST)
NCT02868385 · start 2018-10-01
Registered record
- Registry ID
- NCT02868385
- Conditions
- Schistosomiasis
- Interventions
- 4x Praziquantel; 1x Praziquantel
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2018-10-01
- Completion
- 2019-01-14
- Enrolment
- 167
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchistosomiasisIntervention4x Praziquantel; 1x PraziquantelPhasePhase 3Registry statusCompletedPraziquantel Bioequivalence Study
NCT03437447 · start 2018-06-18
Registered record
- Registry ID
- NCT03437447
- Conditions
- Healthy
- Interventions
- Cisticid; Biltricide
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2018-06-18
- Completion
- 2018-07-06
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionCisticid; BiltricidePhasePhase 1Registry statusCompletedRelative Bioavailability Study of Emodepside IR-tablets and Solution
NCT03383523 · start 2017-10-26
Registered record
- Registry ID
- NCT03383523
- Conditions
- Filariasis
- Interventions
- Emodepside (BAY 44-4400)
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2017-10-26
- Completion
- 2018-03-26
- Enrolment
- 77
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionFilariasisInterventionEmodepside (BAY 44-4400)PhasePhase 1Registry statusCompletedThe Chinese-made Praziquantel for Treatment of Schistosoma Haematobium
NCT03133832 · start 2017-04-10
Registered record
- Registry ID
- NCT03133832
- Conditions
- Schistosomiasis Haematobia
- Interventions
- Companion Tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Unknown
- Start
- 2017-04-10
- Completion
- 2017-07-10
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchistosomiasis HaematobiaInterventionCompanion TabletPhasePhase 3Registry statusUnknownStudy of Safety and Immune Response of the Sm14 Vaccine in Adults of Endemic Regions
NCT03041766 · start 2016-12-06
Registered record
- Registry ID
- NCT03041766
- Conditions
- Schistosomiasis
- Interventions
- Sm14; GLA-SE solution
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2016-12-06
- Completion
- 2017-06-02
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchistosomiasisInterventionSm14; GLA-SE solutionPhasePhase 2Registry statusCompletedSub Arachnoid Neurocysticercosis Treatment Outcome (SANTO)
NCT02947581 · start 2016-11-14
Registered record
- Registry ID
- NCT02947581
- Conditions
- Neurocysticercosis
- Interventions
- Albendazole and praziquantel; Albendazole and praziquantel placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Terminated
- Start
- 2016-11-14
- Completion
- 2021-02-27
- Enrolment
- 107
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionNeurocysticercosisInterventionAlbendazole and praziquantel; Albendazole and praziquantel placeboPhasePhase 3Registry statusTerminatedEffect of Concomitant Mansonella Perstans Microfilaremia on Immune Responses Following Single Dose Praziquantel in People With Schistosomiasis
NCT02734186 · start 2016-04-06
Registered record
- Registry ID
- NCT02734186
- Conditions
- Schistosomiasis
- Interventions
- Praziquantel
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Withdrawn
- Start
- 2016-04-06
- Completion
- 2018-12-14
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchistosomiasisInterventionPraziquantelPhasePhase 4Registry statusWithdrawnAssessing the Effect of Neglected Tropical Diseases on Plasmodium Falciparum Transmission in an Area of Co-endemicity
NCT02769013 · start 2016-04
Registered record
- Registry ID
- NCT02769013
- Conditions
- Malaria Transmission
- Interventions
- Pre-treatment follow up; S. haematobium treatment; Post treatment follow up; Olfactometer experiment
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2016-04
- Completion
- 2020-10
- Enrolment
- 380
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMalaria TransmissionInterventionPre-treatment follow up; S. haematobium treatment; Post treatment follow up; Olfactometer experimentPhaseNot recordedRegistry statusCompletedTaenia Solium Elimination Versus Control: What is the Best Way Forward for Sub-Saharan Africa?
NCT02612896 · start 2016-03
Registered record
- Registry ID
- NCT02612896
- Conditions
- Taenia Solium Infection
- Interventions
- Mass drug administration, praziquantel 10mg/kg; Health education
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2016-03
- Completion
- 2022-02
- Enrolment
- 2,900
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTaenia Solium InfectionInterventionMass drug administration, praziquantel 10mg/kg; Health educationPhaseNot applicableRegistry statusCompletedCross-over Study to Evaluate the Palatability of New Orally Disintegrating Tablets (ODTs) of Praziquantel (PZQ) and L-PZQ Versus Current PZQ Tablets in African Children Age 6-11 Years
NCT02315352 · start 2015-04
Registered record
- Registry ID
- NCT02315352
- Conditions
- Healthy
- Interventions
- L-PZQ ODT; Rac-PZQ ODT; L-PZQ ODT; Rac-PZQ ODT; Cesol®
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2015-04
- Completion
- 2015-05
- Enrolment
- 48
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionL-PZQ ODT; Rac-PZQ ODT; L-PZQ ODT; Rac-PZQ ODT +1 morePhasePhase 1Registry statusCompletedRelative Bioavailability Trial of Oral Dispersible Praziquantel Tablets in Healthy Volunteers
NCT02325713 · start 2015-01
Registered record
- Registry ID
- NCT02325713
- Conditions
- Healthy
- Interventions
- Oral dispersible tablet of praziquantel (ODT-PZQ); Cysticide; ODT-PZQ; ODT-PZQ; ODT-PZQ; Cysticide
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2015-01
- Completion
- 2015-03
- Enrolment
- 32
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionOral dispersible tablet of praziquantel (ODT-PZQ); Cysticide; ODT-PZQ; ODT-PZQ +2 morePhasePhase 1Registry statusCompletedRelative Bioavailability Trial of L-Praziquantel in Healthy Volunteers
NCT02271984 · start 2014-10-31
Registered record
- Registry ID
- NCT02271984
- Conditions
- Healthy
- Interventions
- MSC2499550A; Cysticide; MSC2499550A; MSC2499550A; MSC2499550A; MSC2499550A
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2014-10-31
- Completion
- 2014-12-31
- Enrolment
- 36
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionMSC2499550A; Cysticide; MSC2499550A; MSC2499550A +2 morePhasePhase 1Registry statusCompletedArachidonic Acid Treatment Against Schistosomiasis Infection in Children
NCT02144389 · start 2013-01
Registered record
- Registry ID
- NCT02144389
- Conditions
- Schistosomiasis; Bilharzia
- Interventions
- Praziquantel (PZQ); Arachidonic acid (ARA); PZQ+ARA
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2013-01
- Completion
- 2014-01
- Enrolment
- 335
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchistosomiasis; BilharziaInterventionPraziquantel (PZQ); Arachidonic acid (ARA); PZQ+ARAPhaseNot applicableRegistry statusCompletedSchistosoma Mansoni Morbidity in Children Aged 1-5 Years
NCT01901484 · start 2012-12
Registered record
- Registry ID
- NCT01901484
- Conditions
- Intestinal Schistosomiasis
- Interventions
- Praziquantel
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2012-12
- Completion
- 2014-02
- Enrolment
- 800
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionIntestinal SchistosomiasisInterventionPraziquantelPhasePhase 2Registry statusCompletedImpact IPT With Sulfadoxine-pyrimethamine or Sulfadoxine-pyrimethamine Plus Piperaquine in Schoolchildren
NCT01722539 · start 2012-11
Registered record
- Registry ID
- NCT01722539
- Conditions
- Healthy
- Interventions
- Sulfadoxine-pyrimethamine; Piperaquine; Albendazole; Praziquantel
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2012-11
- Completion
- 2013-11
- Enrolment
- 616
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionSulfadoxine-pyrimethamine; Piperaquine; Albendazole; PraziquantelPhasePhase 3Registry statusCompleted