PHARMACOKINETICS AND PHARMACODYNAMICS OF TUCARESOL, AN ANTISICKLING AGENT, IN HEALTHY-VOLUNTEERS

Citation
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
Citations number
24
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
03065251
Volume
39
Issue
4
Year of publication
1995
Pages
375 - 380
Database
ISI
SICI code
0306-5251(1995)39:4<375:PAPOTA>2.0.ZU;2-O
Abstract
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.