Pe. Rolan et al., PHARMACOKINETICS AND PHARMACODYNAMICS OF TUCARESOL, AN ANTISICKLING AGENT, IN HEALTHY-VOLUNTEERS, British journal of clinical pharmacology, 39(4), 1995, pp. 375-380
1 Tucaresol is an orally administered antisickling agent which increas
es the oxygen affinity of haemoglobin. 2 The pharmacokinetics, effects
on moderate graded exercise and psychometric performance of tucaresol
were examined in a double-blind, placebo-controlled, parallel groups
study in 12 healthy men. 3 Three doses of tucaresol were given at 48 h
intervals intended to modify 15, 25 and 32.5% of a subject's haemoglo
bin to a high affinity form (%MOD). 4 Mean peak %MOD was 34%. Mean C-m
ax values in plasma and erythrocytes were 81.4 and 1459 mu g ml(-1), r
espectively. 5 Heart rate, compared with baseline, increased in the tu
caresol group with the greatest changes at the highest %MOD and worklo
ad. There were no differences between groups in psychometric test perf
ormance. 6 Three volunteers on active drug developed fever, rash and t
ender cervical lymphadenopathy with onset 7-10 days from the start of
dosing, suggesting an immune mechanism. 7 The acute increase in oxygen
affinity with tucaresol is physiologically well-tolerated, but the ut
ility of tucaresol in the management of sickle cell disease will depen
d on the identification of a dosing regimen with a lower incidence of
drug allergy.