Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Nancy Wainman"'
Autor:
C. A. Capier, John Lyons, Karen A. Gelmon, Kim N. Chi, Lesley Seymour, Nancy Wainman, Derek J. Jonker, Susan Dent, Eric X. Chen
Publikováno v:
Investigational New Drugs. 31:1522-1529
Purpose AT9283 is a potent inhibitor of the mitotic regulators, Aurora-kinases A and B, and has shown anti-tumor activity in patients with solid and haematological malignancies. This phase I study assessed safety, tolerability, pharmacokinetic and ph
Autor:
Mark L. Bernstein, Sylvain Baruchel, Darcy Nicksy, Yvan Samson, Elizabeth Eisenhauer, Alexandra P. Zorzi, Nancy Wainman, Sunil Desai, Donna A. Wall
Publikováno v:
Pediatric Blood & Cancer. 60:1868-1874
Background Pracinostat (SB939) is a potent oral inhibitor of class 1, 2, and 4 histone deacetylases (HDAC). The adult recommended phase II dose (RP2D) is 60 mg po three times per week (t.i.w.) for 3 weeks every 4 weeks. This study assessed the toxici
Phase II Trial of SarCNU in Malignant Glioma: Unexpected Pulmonary Toxicity with a Novel Nitrosourea
Autor:
James Perry, Stan Gertler, Gregory Cairncross, Marc Webster, Elizabeth Eisenhauer, Nancy Wainman
Publikováno v:
Investigational New Drugs. 23:591-596
A multi-centre phase II study of SarCNU-a novel chloroethylnitrosourea (CNU)-in patients with recurrent malignant glioma to assess response rate, survival and effects of treatment.Ten patients with histologically proven malignant glioma (seven with g
Autor:
Ian Quirt, Reinhard Lohmann, Elizabeth Eisenhauer, Wendy Walsh, Richard Tozer, Susan Burdette-Radoux, Nancy Wainman, A. Dimitrios Colevas, D. Scott Ernst
Publikováno v:
Investigational New Drugs. 22:315-322
Purpose: To test the activity of the cyclin dependent kinase (cdk) inhibitor flavopiridol in malignant melanoma, a disease with frequent abnormalities of the cyclin dependent kinase system. Patients and methods: Patients had histologically proven, un
Autor:
Nancy Wainman, Gregory Cairncross, Karl Belanger, Samuel K. Ludwin, Elizabeth Eisenhauer, David R. Macdonald, Stan Z. Gertler, Peter A. Forsyth, Susan Burdette-Radoux, Julie Bergeron, Denis Soulières
Publikováno v:
Investigational New Drugs. 21:473-480
To determine the efficacy and toxicity of a novel chemotherapeutic approach with topotecan, a camptothecin analog, for progressive or recurring anaplastic oligodendroglioma or mixed oligoastrocytoma.Patients from seven centers with recurrent or progr
Autor:
M. Maclean, Nisha Mistry, J. M. Besterman, Debbie Ayers, Susan D'Aloisio, Carolyn D. Britten, Nancy Wainman, Elizabeth Eisenhauer, Henry Klamut, Malcolm J. Moore, Patricia S. Firby, Lillian L. Siu, Alison Davis, Karen A. Gelmon, Gregory K. Reid
Publikováno v:
Investigational New Drugs. 21:85-97
Purpose: MG98 is a second generation phosphorothioate antisense oligodeoxynucleotide which is a highly specific inhibitor of translation of the mRNA for human DNA MeTase I (DNMT 1). This phase I study examined the toxicity and pharmacologic profile o
Autor:
Vincent Young, William Steward, Nancy Wainman, Elizabeth Eisenhauer, Reinhard Lohmann, Karl Belanger, Ian Quirt, James J. Rusthoven, Audley Bodurtha
Publikováno v:
Investigational New Drugs. 20:431-437
To determine the tolerability and efficacy of daily oral marimastat (BB-2516 in patients with metastatic melanoma and to determine the matrix metalloproteinase (MMP) activity, tumour necrosis, peri- and intra-tumoral fibrosis and tumor inflammation i
Autor:
Alexandra P, Zorzi, Mark, Bernstein, Yvan, Samson, Donna A, Wall, Sunil, Desai, Darcy, Nicksy, Nancy, Wainman, Elizabeth, Eisenhauer, Sylvain, Baruchel
Publikováno v:
Pediatric bloodcancer. 60(11)
Pracinostat (SB939) is a potent oral inhibitor of class 1, 2, and 4 histone deacetylases (HDAC). The adult recommended phase II dose (RP2D) is 60 mg po three times per week (t.i.w.) for 3 weeks every 4 weeks. This study assessed the toxicities and ph
Autor:
Antonio Grillo-Lopez, Lloyd R. Whitfield, Jacques Jolivet, Karl Belanger, David J. Stewart, Jean A. Maroun, Nancy Wainman, Elizabeth Eisenhauer
Publikováno v:
Investigational New Drugs. 11:301-308
DUP-937 is a new anthrapyrazole intercalator that inhibits DNA synthesis. A phase I trial was conducted in which DUP-937 was given in an intravenous bolus weekly for 3 weeks. Cycles were repeated every 5 weeks. Twenty men and 13 women with median ECO
Autor:
Ron Feld, C. Cripps, James Joseph Biagi, Timothy W. Synold, Jennifer J. Knox, Lesley Seymour, Pierre Major, Sharlene Gill, Nancy Wainman, Elizabeth Eisenhauer
Publikováno v:
Investigational new drugs. 26(3)
Hepatocellular carcinoma (HCC) remains a lethal treatment-resistant cancer with a median survival of