Epidemic and endemic meningitis caused by group A Neisseria meningitidis remains a problem in subSaharan Africa. Although group A meningococcal capsular polysaccharide (GAMP) vaccine confers immunity at all ages, the improved immunogenicity of a conjugate and its compatibility with the World Health Organization's Extended Program on Immunization offers advantages over GAMP alone. Conjugates of GAMP bound to bovine serum albumin (BSA) were synthesized, characterized, and evaluated for their immunogenicities in mice. Two methods, involving adipic acid dihydrazide (ADH) as a linker, were used. First, ADH was bound to GAMP activated with cyanogen bromide (CNBr) or with 1-cyano-4(dimethylamino)-pyridinium tetrafluoroborate (CDAP) to form GAMP CNBr AH and GAMP CDAP AH. These derivatives were bound to BSA by 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) to form GAMP CNBr AH-BSA and GAMP CDAP AH-BSA. Second, ADH was bound to BSA with EDC to form AHBSA. AHBSA was bound to activated GAMP to form GAMP CNBr -AHBSA and GAMP CDAP -AHBSA. The yield of GAMP CDAP -AHBSA (35 to 40%) was higher than those of the other conjugates (5 to 20%). GAMP conjugates elicited immunoglobulin G (IgG) anti-GAMP in all mice after three injections of 2.5 or 5.0 g of GAMP: the geometric mean (GM) was highest in recipients of GAMP CDAP -AHBSA (11.40 enzyme-linked immunosorbent assay units). Although the difference was not statistically significant, the 5.0-g dose elicited a higher GM IgG anti-GAMP than the 2.5-g dose. Low levels of anti-GAMP were elicited by GAMP alone. GAMP CDAP -AHBSA elicited bactericidal activity roughly proportional to the level of IgG anti-GAMP.