Experiment 421145

Details

PropertyValue
Pharmacology
Administration routeIP
OrganismEmpty organism
CitationMARKMAN,M: ROWINSKY,E: HAKES,T: REICHMAN,B: JONES,W: LEWIS JR,JL: RUBIN,S: CURTIN,J: BARAKAT,R: PHILLIPS,M: HUROWITZ,L: ALMADRONES,L: HOSKINS,W:. (1992). PHASE I TRIAL OF INTRAPERITONEAL TAXOL: A GYNECOLOIC ONCOLOGY GROUP STUDY.. 10(9)
Amount utilized
Compound isolated
Disease25 PATIENTS WERE ENTERED INTO THIS PHASE ONE STUDY. 24 PATIENTS HAD OVARIAN CANCER AND 1 PATIENT HAD BREAST CANCER. PATIENTS WERE DOSED EVERY 3-4 WEEKS. TOXICITIES INCLUDED BONE MARROW SUPPRESSION, WBC COUNT DECREASE, NEUTROPENIC FEVERS, SKIN RASHES WITH DOSE LIMITING TOXICITY OF ABDOMINAL PAIN. 2 PATIENTS EXHIBITED COMPLETE DISAPPEARANCE OF SIGNIFICANT PRETREATMENT ASCITES. 6 PATIENTS HAD SIGNIFICANT REDUCTIONS IN SERUM CA-125 ANTIGEN.
Dose amount>175 MG
Number1
Qualitative result.
AnimalHUMAN ADULT
Per unitSQ M
Dose expressionDOSE