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Characterization of the pharmacokinetics of bisantrene (NSC-337766)

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Summary

The pharmacokinetics of bisantrene, 9,10-anthracenedicarboxaldehyde bis ((4,5-dihydro-1 H-imidazol-2-yl) hydrazone) dihydrochloride were evaluated during a Phase I clinical investigation. Bisantrene at doses of 20 to 280 mg/m2 was administered by variable infusion rates to nine patients with advanced metastatic cancer. Bisantrene's plasma clearance followed a triexponential pattern with a harmonic mean terminal half-life (t1/2 γ) of 26 h. The steady state volume of distribution (Vd ss ) was large, averaging 627 l/m2. Plasma clearance averaged 42.6±6.7 l/h/m2. The cumulative urinary excretion of bisantrene was 3.6±1.6% at 48 h.

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Kuhn, J.G., Ludden, T.M., Myers, J.W. et al. Characterization of the pharmacokinetics of bisantrene (NSC-337766). Invest New Drugs 1, 253–258 (1983). https://doi.org/10.1007/BF00208899

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