Related Experiment Video
Updated: Aug 15, 2026

Reduced Itraconazole Concentration and Durations Are Successful in Treating Batrachochytrium dendrobatidis Infection in Amphibians
Published on: March 14, 2014
Ivermectin: a long-acting microfilaricidal agent
E I Ette1, W O Thomas, J I Achumba
1University of Lagos, Nigeria.
Abstract:
Ivermectin is a macrocyclic lactone (fermentation) product and actinomycete (Streptomyces avermitilis) that possesses an unusually broad spectrum of potent activity against several species of nematodes, arachnids, and insects that parasitize domestic animals. From clinical trials in humans it has been found to be microfilaricidal, killing microfilariae of Onchocerca volvulus (the parasite causing onchocerciasis), and interrupting its transmission by the black fly vector. Dermal microfilariae density in patients are reduced to near zero levels for 6-12 months after a single oral dose of ivermectin 0.15-0.2 mg/kg. Its precise mechanism of action is unknown. It has a time to maximum concentration of 2.7-4.3 h, and an elimination half-life of 28 +/- 10 h. When compared with an oral solution the tablet dosage form has a relative bioavailability of approximately 60 percent. Not much is known about its metabolism in humans, and the unchanged drug is not detected in the urine. Controlled clinical trials have shown ivermectin to be associated with milder side effects than diethylcarbamazine, the current drug of choice for onchocerciasis therapy. It does not cause the severe Mazzoti-type (anaphylactoid) reactions that are associated with diethylcarbamazine use. Ivermectin is effective, safer, and more tolerable than diethylcarbamazine. It should, therefore, replace diethylcarbamazine as the drug of choice for onchocerciasis therapy.
Insights
Ivermectin effectively kills Onchocerca volvulus microfilariae, reducing transmission and offering a safer alternative to diethylcarbamazine for onchocerciasis treatment.
Area of Science:
- Pharmacology
- Parasitology
- Tropical Medicine
Background:
- Ivermectin is a potent macrocyclic lactone with broad-spectrum activity against parasites.
- Onchocerciasis, caused by Onchocerca volvulus, is a significant public health concern transmitted by black flies.
- Diethylcarbamazine is the current standard treatment but is associated with severe Mazzoti-type reactions.
Purpose of the Study:
- To evaluate the efficacy and safety of ivermectin in treating onchocerciasis.
- To compare ivermectin's side effect profile with diethylcarbamazine.
Main Methods:
- Clinical trials involving oral administration of ivermectin (0.15-0.2 mg/kg).
- Assessment of microfilaricidal activity and reduction in dermal microfilariae density.
- Comparison of adverse event profiles between ivermectin and diethylcarbamazine.
Main Results:
- Ivermectin demonstrated significant microfilaricidal activity, reducing dermal microfilariae density to near zero for 6-12 months post-dose.
- The drug exhibited a favorable pharmacokinetic profile with a rapid time to maximum concentration and a defined elimination half-life.
- Controlled trials indicated ivermectin is associated with milder side effects compared to diethylcarbamazine, notably lacking severe Mazzoti-type reactions.
Conclusions:
- Ivermectin is an effective and safer alternative for onchocerciasis therapy.
- The drug's superior tolerability profile warrants its adoption as the preferred treatment over diethylcarbamazine.
Related Concept Videos
Rocky Mountain Spotted Fever
American Trypanosomiasis
Giardiasis
Antifungal Agents
Anthelminthic Agents
Antiprotozoal Agents

