Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Richard S. Ungerleider"'
Autor:
Richard S. Ungerleider, Elisabeth I. Heath, Amy Weise, Ulka N. Vaishampayan, Yasuo Urata, Dailan Danforth
Publikováno v:
Investigational New Drugs. 40:300-307
Background Dysregulation of histone deacetylases (HDACs) is common in cancer and is critical to the development and progression of the majority of tumors. This first-in-human Phase Ia study assessed the safety, efficacy, and pharmacokinetics (PK) of
Autor:
Vincent Chung, Henry J. Durivage, Fadi Braiteh, Donald A. Richards, Francis Johnson, John S. Kovach, Richard S. Ungerleider, Aaron S. Mansfield
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 23(13)
Purpose: To determine the MTD and to assess the safety, tolerability, and potential activity of LB-100, a first-in-class small-molecule inhibitor of protein phosphatase 2A (PP2A) in adult patients with progressive solid tumors. Experimental Design: L
Autor:
Richard S. Ungerleider, Rogerio I. Neves, John T. Vetto, Maki Tanaka, Matthew H. Taylor, Robert H.I. Andtbacka, Sanjiv S. Agarwala, Adil Daud, Merrick I. Ross, Hung T. Khong
Publikováno v:
Journal of Clinical Oncology. 36:9541-9541
9541Background: HF10, a bioselected replication-competent oncolytic virus derived from HSV-1, has been evaluated in combination with ipilimumab (ipi) in a Phase II trial (NCT02272855) in unresectab...
Publikováno v:
Wiley StatsRef: Statistics Reference
The clinical trials cooperative group program was established by the US National Cancer Institute in 1955. The number of groups increased to 18 by 1985 and then decreased to 11. This article describes the work of the groups since the mid-1980s. It co
Autor:
Adil Daud, Matthew H. Taylor, John T. Vetto, Robert H.I. Andtbacka, Kenneth F. Grossmann, Hung Thieu Khong, Rogerio I. Neves, Merrick I. Ross, Maki Tanaka, Richard S. Ungerleider, Sanjiv S. Agarwala
Publikováno v:
Annals of Oncology. 28:x113
Autor:
Hung T. Khong, Richard S. Ungerleider, Sanjiv S. Agarwala, Robert H.I. Andtbacka, Adil Daud, Kenneth F. Grossmann, Merrick I. Ross, John T. Vetto, Matthew H. Taylor, Maki Tanaka, Rogerio I. Neves
Publikováno v:
Journal of Clinical Oncology. 35:9510-9510
9510 Background: HF10 is a bioselected replication-competent oncolytic virus derived from HSV-1. Herein, we report the safety and efficacy data of HF10 + ipilimumab (ipi) combination treatment in a Phase II trial in melanoma. Methods: Key entry crite
Publikováno v:
Journal of Clinical Oncology. 15:2736-2743
PURPOSE To describe the rationale for independent data monitoring committees (DMCs) for National Cancer Institute (NCI)-sponsored phase III cooperative group clinical trials. DESIGN We review the necessity for interim monitoring of outcome data durin
Publikováno v:
The Oncologist. 1:293-304
Since the formulation of the “dose-intensity” concept of anticancer therapy in the mid-1980s, the concept that “more is better” has gained general acceptance among pediatric oncologists. However, recently published clinical trials results for
Autor:
Diane C. Arthur, David G. Tubergen, G Reamon, Michael P. Link, Stephen E. Sallan, Harland N. Sather, Jonathan J. Shuster, Bruce M. Camitta, Andrew J. Carroll, Richard M. Simon, Fatih M. Uckun, Richard D. Gelber, Nyla A. Heerema, Sharon E. Murphy, C H Pui, Paul S. Gaynon, Michael E. Trigg, Richard S. Ungerleider, Edward L. Korn, M Smith, J Pullen, W M Crist
Publikováno v:
Journal of Clinical Oncology. 14:18-24
PURPOSE To define more uniform criteria for risk-based treatment assignment for children with acute lymphoblastic leukemia (ALL), the Cancer Therapy Evaluation Program (CTEP) of the National Cancer Institute (NCI) sponsored a workshop in September 19