Literature DB >> 7640143

Pharmacokinetics and pharmacodynamics of tucaresol, an antisickling agent, in healthy volunteers.

P E Rolan1, A J Mercer, R Wootton, J Posner.   

Abstract

1. Tucaresol is an orally administered antisickling agent which increases 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 haemoglobin to a high affinity form (%MOD). 4. Mean peak %MOD was 34%. Mean Cmax values in plasma and erythrocytes were 81.4 and 1459 micrograms ml-1, respectively. 5. Heart rate, compared with baseline, increased in the tucaresol group with the greatest changes at the highest %MOD and workload. There were no differences between groups in psychometric test performance. 6. Three volunteers on active drug developed fever, rash and tender 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 utility of tucaresol in the management of sickle cell disease will depend on the identification of a dosing regimen with a lower incidence of drug allergy.

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Year:  1995        PMID: 7640143      PMCID: PMC1365124          DOI: 10.1111/j.1365-2125.1995.tb04465.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  18 in total

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2.  Is there treatment for sickle cell anemia?

Authors:  O S Platt
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Authors:  G Borg
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5.  Effect of BW12C on oxygen affinity of haemoglobin in sickle-cell disease.

Authors:  A J Keidan; I M Franklin; R D White; M Joy; E R Huehns; J Stuart
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6.  The pharmacokinetics, tolerability and pharmacodynamics of tucaresol (589C80; 4[2-formyl-3-hydroxyphenoxymethyl] benzoic acid), a potential anti-sickling agent, following oral administration to healthy subjects.

Authors:  P E Rolan; J E Parker; S J Gray; B C Weatherley; J Ingram; W Leavens; R Wootton; J Posner
Journal:  Br J Clin Pharmacol       Date:  1993-04       Impact factor: 4.335

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Authors:  K Schaffler; W Klausnitzer
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8.  Characterization of the binding of the anti-sickling compound, BW12C, to haemoglobin.

Authors:  M Merrett; D K Stammers; R D White; R Wootton; G Kneen
Journal:  Biochem J       Date:  1986-10-15       Impact factor: 3.857

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7.  Design, Synthesis, and Biological Evaluation of Ester and Ether Derivatives of Antisickling Agent 5-HMF for the Treatment of Sickle Cell Disease.

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Review 8.  New developments in anti-sickling agents: can drugs directly prevent the polymerization of sickle haemoglobin in vivo?

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