Table 3. Immediate research priorities.
| Disease | Research Goal | Feasibility (0–10a: 0, Impossible; 10, Inevitable) | Impact if Achieved (0–10a: 0, None; 10, Massive) | 
| Lymphatic filariasis | Development of antigen tests to usable/reliable format | 9 | 8 if ≤USD 0.50 | 
| Development and validation of tests (e.g., IgG4-subclass antibody detection tests using recombinant Bm14, BmR1, WbSXP, and W. bancrofti-specific antigens [20] or PCR-based detection of parasite DNA in homogenised mosquitoes [21]) useful for post-elimination surveillance, with accompanying standardised survey methodologies | 9 | 8 if ≤USD 0.50 | |
| Trachoma | Development of a test for ocular C. trachomatis infection [22] able to maintain specificity at high temperatures and low humidity [23] | 9 | 8 if ≤USD 0.50 | 
| Development of eye/nose swab-, saliva-, or blood-based anti-C. trachomatis antibody test and exploration of the impact of successful trachoma control on antibody profiles in endemic populations | 3 | 5 | |
| Development and validation of a school-based survey protocol (need threshold minimum school attendance) | 7 | 8 | |
| Schistosomiasis | Development of antigen [24] or antibody [25] isotype combination(s) useful in high and low transmission intensity environments, able to distinguish current from past infection | 8 | 9 | 
| Development of antigen or antibody isotype combination(s) to distinguish between different species | 8 | 4 | |
| Development of serum markers of morbidity | 6 | 8 | |
| Soil-transmitted helminthiases | Development of reliable blood- or urine-based assays for detection of current infection | 4 | 9 | 
| Development of serum markers of morbidity | 6 | 8 | |
| Onchocerciasis | Development of a quantitative antigen test for use in endemic areas in Africa and validation of Ov16 antibody test for demonstrating interruption of transmission in Africa | 5 | 8 | 
| Development of a test for loaiasis | 5 | 9 | 
Determined by expert consensus.