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Study identifier: NCT06350851 Synced from ClinicalTrials.gov · July 29, 2026
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Development of a New Rapid Diagnostic Test to Support Onchocerciasis Elimination

Condition: Onchocerciasis · Loiasis · Mansonelliasis  ·  Sponsor: Bioaster

PhaseNA
Planned participants400
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

Onchocerciasis, also known as river blindness, is one of the disease targeted for elimination by the World Health Organization (WHO) in the group of Neglected Tropical Diseases. Existing diagnostic tools for onchocerciasis have limitations that make mapping, epidemiological assessments and verification of elimination of onchocerciasis difficult. It is in this context that WHO, in its 2021-2030 roadmap for onchocerciasis, has identified the development of new diagnostic tests, or the improvement of existing diagnostic tests, as a critical condition for achieving the goal of eliminating onchocerciasis transmission. To this end, a series of cross-sectional studies will be carried out in Cameroun over a one year period to collect and characterize biological samples for the development and evaluation of a new rapid diagnostic test for onchocerciasis. The study will target individuals aged 18 and over, mono-infected with one of the filarial species Onchocerca volvulus, Loa loa or Mansonella perstans; and non-infected. At the end of this study, data on the endemicity of onchocerciasis, loiasis and mansonellosis in the selected communities will be updated. More importantly, a new rapid diagnostic test will be developed, which can then be used to monitor the activities of onchocerciasis control programs.

This description comes directly from the study's public registry record.

Talk to the study team

Marie KOENIG  ·  +33634452334  ·  marie.koenig@bioaster.org

Marion DARNAUD  ·  +33481111002  ·  marion.darnaud@bioaster.org

Always discuss trial participation with your own doctor first.

Locations (1)

Higher Institute for Scientific and Medical ResearchYaoundé, CameroonRecruiting

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Source record: clinicaltrials.gov/study/NCT06350851