The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
The potential impact of moxidectin on onchocerciasis elimination in Africa: an economic evaluation based on the Phase II clinical trial data
Open accessAbstract
BACKGROUND: Spurred by success in several foci, onchocerciasis control policy in Africa has shifted from morbidity control to elimination of infection. Clinical trials have demonstrated that moxidectin is substantially more efficacious than ivermectin in effecting sustained reductions in skin microfilarial load and, therefore, may accelerate progress towards elimination. We compare the potential cost-effectiveness of annual moxidectin with annual and biannual ivermectin treatment. METHODS: Data from the first clinical study of moxidectin were used to parameterise the onchocerciasis transmission model EPIONCHO to investigate, for different epidemiological and programmatic scenarios in African savannah settings, the number of years and in-country costs necessary to reach the operational thresholds for cessation of treatment, comparing annual and biannual ivermectin with annual moxidectin treatment. RESULTS: Annual moxidectin and biannual ivermectin treatment would achieve similar reductions in programme duration relative to annual ivermectin treatment. Unlike biannual ivermectin treatment, annual moxidectin treatment would not incur a considerable increase in programmatic costs and, therefore, would generate sizeable in-country cost savings (assuming the drug is donated). Furthermore, the impact of moxidectin, unlike ivermectin, was not substantively influenced by the timing of treatment relative to seasonal patterns of transmission. CONCLUSIONS: Moxidectin is a promising new drug for the control and elimination of onchocerciasis. It has high programmatic value particularly when resource limitation prevents a biannual treatment strategy, or optimal timing of treatment relative to peak transmission season is not feasible.
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Cites
Lymphatic filariasis and onchocerciasis
Taylor, M. J., Hoerauf, A., & Bockarie, M. (2010) · The Lancet · doi:10.1016/s0140-6736(10)60586-7 · Cited by 686 · cited 2×
“This highlights the need for drugs without microfilaricidal activity [24-26] and complementary vector control strategies for L.”
BackgroundMoxidectin and the avermectins: Consanguinity but not identity
Prichard, R., Ménez, C., & Lespine, A. (2012) · International Journal for Parasitology: Drugs and Drug Resistance · doi:10.1016/j.ijpddr.2012.04.001 · Cited by 439
Cited by
Mechanical Strain and Bone Cell Function: A Review
Ehrlich, P. J., & Lanyon, L. E. (2002) · Osteoporosis International · doi:10.1007/s001980200095 · Cited by 512
Opoku, N. O., Bakajika, D. K., Kanza, E. M., Howard, H., Mambandu, G. L., Nyathirombo, A., Nigo, M. M., Kasonia, K., Masembe, S. L., Mumbere, M., et al. (2018) · The Lancet · doi:10.1016/s0140-6736(17)32844-1 · Cited by 304
Self-citationMoxidectin: an oral treatment for human onchocerciasis
Milton, P., Hamley, J. I. D., Walker, M., & Basáñez, M.-G. (2020) · Expert Review of Anti-infective Therapy · doi:10.1080/14787210.2020.1792772 · Cited by 211
Batsa Debrah, L., Klarmann-Schulz, U., Osei-Mensah, J., Dubben, B., Fischer, K., Mubarik, Y., Ayisi-Boateng, N. K., Ricchiuto, A., Fimmers, R., Konadu, P., et al. (2020) · Clinical Infectious Diseases · doi:10.1093/cid/ciz889 · Cited by 28
Metadata
- Authors
- Turner, H. C., Walker, M., Attah, S. K., Opoku, N. O., Awadzi, K., Kuesel, A. C., & Basáñez, M.-G.
- Venue
- Parasites & Vectors
- Published
- 2015-03-19
- Volume
- 8
- Issue
- 1
- Pages
- 167-167
- ISSN
- 1756-3305 (ISSN-L)
- OpenAlex
- W2004422663
- Cited by
- 194
- References
- 2
- FWCI
- 12.29
- Type
- journal article
- Language
- en
- Open access
- gold
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- Turner, H. C., Walker, M., Attah, S. K., Opoku, N. O., Awadzi, K., Kuesel, A. C., & Basáñez, M.-G. (2015). The potential impact of moxidectin on onchocerciasis elimination in Africa: an economic evaluation based on the Phase II clinical trial data. Parasites & Vectors. https://doi.org/10.1186/s13071-015-0779-4
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