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Published on: August 16, 2011
Praziquantel: a new schistosomicide against Schistosoma haematobium
Insights
Praziquantel is a highly effective new schistosomicide for treating Schistosoma haematobium in African schoolchildren, with few side effects. Further research is needed to determine the optimal dose for children with high initial worm egg counts.
Area of Science:
- * Tropical Medicine
- * Infectious Diseases
- * Pharmacology
Background:
- * Schistosomiasis haematobium is a significant parasitic disease affecting schoolchildren in many parts of Africa.
- * The development of effective and safe treatments is crucial for controlling this neglected tropical disease.
Purpose of the Study:
- * To evaluate the efficacy and safety of praziquantel in treating Schistosoma haematobium infection in African schoolchildren.
- * To compare different praziquantel dosing regimens: single doses (30 and 40 mg/kg) and a split dose (2 x 20 mg/kg).
Main Methods:
- * African schoolchildren with Schistosoma haematobium infection were enrolled.
- * Participants were stratified by infection severity and randomly assigned to one of three praziquantel treatment groups.
- * Treatment outcomes and side effects were monitored.
Main Results:
- * All three praziquantel regimens demonstrated high effectiveness in treating Schistosoma haematobium.
- * The drug exhibited a favorable safety profile with minimal side effects across all tested doses.
- * Children with very high pretreatment egg loads showed a less robust therapeutic response, suggesting a need for dose optimization.
Conclusions:
- * Praziquantel is a highly effective and safe schistosomicide for Schistosoma haematobium infections in children.
- * Single-dose regimens are effective, but optimal dosing may need adjustment for individuals with high initial parasite burdens.
- * Praziquantel shows promise as an ideal treatment for schistosomiasis due to its efficacy, safety, and ease of administration.
Abstract:
The effectiveness of the new schistosomicide praziquantel was assessed in African schoolchildren infected with Schistosoma haematobium. They were stratified according to the severity of their infection and were then randomly allocated to treatment with two single-dose regimens (30 and 40 mg/kg) and a split regimen of two doses of 20 mg/kg given four hours apart. All three regimens were highly effective and produced few side effects. Children who initially had very high pretreatment egg loads showed a poorer therapeutic response at all dose levels, and further investigations are necessary to find the optimum dose. Because of its effectiveness in a single dose and lack of toxicity, praziquantel may prove to be the ideal schistosomicide.
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