|1.||Sloan, Jeff A: 1 article (01/2003)|
|2.||Alberts, Steven R: 1 article (01/2003)|
|3.||Dorr, F Andrew: 1 article (01/2003)|
|4.||Dy, Grace K: 1 article (01/2003)|
|5.||Pitot, Henry C: 1 article (01/2003)|
|6.||Adjei, Alex A: 1 article (01/2003)|
|7.||Holmlund, Jon: 1 article (01/2003)|
|8.||Hanson, Lorelei J: 1 article (01/2003)|
|9.||Goldberg, Richard M: 1 article (01/2003)|
|10.||Erlichman, Charles: 1 article (01/2003)|
09/01/2001 - "ISIS 2503 is a 20-base antisense phosphorothioate oligodeoxyribonucleotide that specifically downregulates H-ras expression and inhibits tumor cell growth in preclinical studies. "
09/01/2001 - "Several patients had stabilization of disease, suggesting that ISIS 2503 had some tumor growth inhibitory effects and future trials of ISIS 2503 in combination with chemotherapy should be considered."
09/01/2001 - "Here, the authors report an initial clinical study of the safety and tolerability of an intravenous infusion of ISIS 2503 in patients with advanced cancer. "
09/01/2001 - "A continuous intravenous infusion of ISIS 2503 was administered for 14 days every 3 weeks to 23 patients with a variety of solid tumors refractory to standard therapy. "
01/01/2003 - "The purpose of this study was to define the toxicity, pharmacokinetics, and clinical activity of the combination of ISIS 2503, an oligodeoxynucleotide antisense inhibitor of H-ras, and gemcitabine in patients with advanced solid tumors. "
09/01/2001 - "A Phase I trial of H-ras antisense oligonucleotide ISIS 2503 administered as a continuous intravenous infusion in patients with advanced carcinoma."
11/08/1996 - "Gene-specific oligonucleotides (oligos) against c-Ki-RAS (ISIS 6957), c-Ha-RAS (ISIS 2503), and oncogenic Ha-RAS (ISIS 2570) were used to analyze the requirement for individual RAS proteins in the proliferation of diploid human lung fibroblasts (MRC-5), and human bladder carcinoma cell lines with (T24) or without (J-82) a RAS mutation. "
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|2.||Drug Therapy (Chemotherapy)