Search Results - "RUBIN, Eric H"

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    Drug development and clinical trials—the path to an approved cancer drug by Rubin, Eric H., Gilliland, D. Gary

    Published in Nature reviews. Clinical oncology (01-04-2012)
    “…The current system for the development of anticancer drugs is not fit for purpose. In this Review article, this system is examined from the perspective of the…”
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    Rendering the 3 + 3 Design to Rest: More Efficient Approaches to Oncology Dose-Finding Trials in the Era of Targeted Therapy by Nie, Lei, Rubin, Eric H, Mehrotra, Nitin, Pinheiro, José, Fernandes, Laura L, Roy, Amit, Bailey, Stuart, de Alwis, Dinesh P

    Published in Clinical cancer research (01-06-2016)
    “…Selection of the maximum tolerated dose (MTD) as the recommended dose for registration trials based on a dose-escalation trial using variations of an MTD/3 + 3…”
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    Epothilones: Mechanism of Action and Biologic Activity by GOODIN, Susan, KANE, Michael P, RUBIN, Eric H

    Published in Journal of clinical oncology (15-05-2004)
    “…Drugs that target microtubules are among the most commonly prescribed anticancer therapies. Although the mechanisms by which perturbation of microtubule…”
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    Phase I Study of Eribulin Mesylate Administered Once Every 21 Days in Patients with Advanced Solid Tumors by Tan, Antoinette R, Rubin, Eric H, Walton, Diana C, Shuster, Dale E, Wong, Y Nancy, Fang, Fang, Ashworth, Simon, Rosen, Lee S

    Published in Clinical cancer research (15-06-2009)
    “…Purpose: To evaluate the maximum tolerated dose (MTD), dose-limiting toxicities (DLT), and pharmacokinetics of eribulin mesylate (E7389), a halichondrin B…”
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    From Famine to Feast: Developing Early-Phase Combination Immunotherapy Trials Wisely by Day, Daphne, Monjazeb, Arta M, Sharon, Elad, Ivy, S Percy, Rubin, Eric H, Rosner, Gary L, Butler, Marcus O

    Published in Clinical cancer research (01-09-2017)
    “…Not until the turn of this century has immunotherapy become a fundamental component of cancer treatment. While monotherapy with immune modulators, such as…”
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    Clinical pharmacology profile of vorinostat, a histone deacetylase inhibitor by Iwamoto, Marian, Friedman, Evan J., Sandhu, Punam, Agrawal, Nancy G. B., Rubin, Eric H., Wagner, John A.

    Published in Cancer chemotherapy and pharmacology (01-09-2013)
    “…Purpose Vorinostat is a histone deacetylase inhibitor that has demonstrated preclinical activity in numerous cancer models. Clinical activity has been…”
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    Mechanisms of resistance to topoisomerase I-targeting drugs by Rasheed, Zeshaan A, Rubin, Eric H

    Published in Oncogene (20-10-2003)
    “…DNA topoisomerases are a class of enzymes that alter the topology of DNA and are targets of several anticancer drugs. Camptothecins (CPTs) are a relatively new…”
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    Topors Functions as an E3 Ubiquitin Ligase with Specific E2 Enzymes and Ubiquitinates p53 by Rajendra, Rajeev, Malegaonkar, Diptee, Pungaliya, Pooja, Marshall, Henderson, Rasheed, Zeshaan, Brownell, James, Liu, Leroy F, Lutzker, Stuart, Saleem, Ahamed, Rubin, Eric H

    Published in The Journal of biological chemistry (27-08-2004)
    “…The human topoisomerase I- and p53-binding protein topors contains a highly conserved, N-terminal C3HC4-type RING domain that is homologous to the RING domains…”
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    Pharmacokinetics of Cetuximab After Administration of Escalating Single Dosing and Weekly Fixed Dosing in Patients with Solid Tumors by TAN, Antoinette R, MOORE, Dirk F, HIDALGO, Manuel, DOROSHOW, James H, POPLIN, Elizabeth A, GOODIN, Susan, MAURO, David, RUBIN, Eric H

    Published in Clinical cancer research (01-11-2006)
    “…Purpose: Previous studies of cetuximab pharmacokinetics did not fully characterize its elimination phase. The purpose of this trial was to evaluate the…”
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    A Single Supratherapeutic Dose of Vorinostat Does Not Prolong the QTc Interval in Patients with Advanced Cancer by Munster, Pamela N, Rubin, Eric H, Van Belle, Simon, Friedman, Evan, Patterson, Jaclyn K, Van Dyck, Kristien, Li, Xiadong, Comisar, Wendy, Chodakewitz, Jeffery A, Wagner, John A, Iwamoto, Marian

    Published in Clinical cancer research (15-11-2009)
    “…Purpose: This dedicated QTc phase I study, conducted in advanced-stage cancer patients, assessed the effect of a single supratherapeutic dose (800 mg) of…”
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    Phase I Dose-Finding Study of Weekly Single-Agent Patupilone in Patients With Advanced Solid Tumors by RUBIN, Eric H, ROTHERMEL, John, TESFAYE, Fisseha, TIANLING CHEN, HUBERT, Martine, HO, Yu-Yun, HSU, Chyi-Hung, OZA, Amit M

    Published in Journal of clinical oncology (20-12-2005)
    “…To evaluate the safety and maximum-tolerated dose (MTD) of weekly patupilone, a natural epothilone B, in patients with advanced solid tumors. Patients were…”
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    The BATTLE trial: a bold step toward improving the efficiency of biomarker-based drug development by Rubin, Eric H, Anderson, Keaven M, Gause, Christine K

    Published in Cancer discovery (01-06-2011)
    “…Successful completion of the Biomarker-integrated Approaches of Targeted Therapy for Lung Cancer Elimination (BATTLE) trial, reported in this issue of Cancer…”
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    Adaptive phase 2/3 designs for oncology drug development – Time to hedge by Chen, Cong, Rubin, Eric H.

    Published in Contemporary clinical trials (01-02-2023)
    “…Randomized-controlled Phase 2 trials are routinely skipped in oncology drug development in favor of directly going to confirmatory Phase 3 after…”
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    Ubiquitination by TOPORS Regulates the Prostate Tumor Suppressor NKX3.1 by Guan, Bin, Pungaliya, Pooja, Li, Xiang, Uquillas, Carlos, Mutton, Laura N., Rubin, Eric H., Bieberich, Charles J.

    Published in The Journal of biological chemistry (22-02-2008)
    “…The NKX3.1 gene located at 8p21.2 encodes a homeodomain-containing transcription factor that acts as a haploinsufficient tumor suppressor in prostate cancer…”
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    Finding the Right Dose for Cancer Therapeutics—Can We Do Better? by Rubin, Eric H, Anderson, Keaven M

    Published in Clinical cancer research (15-02-2010)
    “…Unlike other diseases, dose-selection for cancer therapeutics is often based on the maximum-tolerated dose in phase 1 studies involving relatively few…”
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