Experiment 891539

Details

PropertyValue
Pharmacology
Administration routeIV INFUSION
OrganismEmpty organism
CitationKUHN,JG: VON HOFF,DD: HERSH,M: MELINK,T: CLARK,GM: WEISS,GR: COLTMAN,CA:. (1989). PHASE I TRIAL OF ECHINOMYCIN (NSC 526417), A BIFUNCTIONAL INTERCALATING AGENT,S ADMINISTERED BY 24-HOUR CONTINUOUS INFUSION.. 25(5)
Amount utilized
Compound isolated
Disease43 PATIENTS WITH ADVANCED CANCER WERE STUDIED. THE DOSE-LIMITING TOXICITIES OF THE DRUG ADMINISTERED AS A 24 HR CONTINUOUS INFUSION EVERY 28 DAYS WERE NAUSEA AND VOMITING BEGINNING AT THE END OF THE 24 HR INFUSION AND LASTING FROM 3 TO 8 DAYS. OTHER TOXICITIES INCLUDED SPORADIC THROMOBOCYTOPENIA AND BIOCHEMICAL EVIDENCE OF LIVER DYSFUNCTION CHARACTERIZED BY ELEVATION IN SGOT. PERIPHERAL VEIN PHLEBITIS WAS NOTED IN 100% OF PATIENTS, AND WATERY DIARRHEA OF 24-48 HR DURATION WAS NOTED IN 7% OF PATIENTS.
Dose amount2.13 MG
Number1
Qualitative resultACTIVE
AnimalHUMAN ADULT
Per unitSQ M BODY SURFACE
Dose expressionMAXIMUM TOLERATED DOSE