Experiment 445740

Details

PropertyValue
Pharmacology
Administration routeIV INFUSION
OrganismEmpty organism
CitationBLANEY,SM: BALIS,FM: COLE,DE: CRAIG,C: REID,JM: AMES,MM: KRAILO,M: REAMAN,G: HAMMOND,D: POPLACK,DG:. (1993). PEDIATRIC PHASE I TRIAL AND PHARMACOKINETIC STUDY OF TOPOTECAN ADMINISTERED AS A 24-HOUR CONTINUOUS INFUSION.. 53(5)
Amount utilized
Compound isolated
Disease29 PEDIATRIC PATIENTS WITH REFRACTORY MALIGNANCIES WERE USED IN THIS PHASE 1 STUDY. PATIENTS WERE GIVEN DOSES RANGING FROM 2.0 TO 7.5 MG/SQ.M. EVERY 21 DAYS. THE PATIENTS EXPERIENCED DOSE LIMITING THROMBOCYTOPENIA AND NEUTROPENIA. NO OTHER DOSE LIMITING TOXICITIES WERE OBSERVED. NAUSEA AND VOMITING WERE MILD AND OCCURED IN <20% AND 10% OF PATIENTS RESPECTIVELY. NO OBJECTIVE RESPONSES WERE OBSERVED.
Dose amountVAR
Number1
Qualitative result.
AnimalHUMAN ADULT
Dose expressionDOSE