Strategies for Derisking Translational Processes for Biomedical Technologies.
暂无分享,去创建一个
Georg N Duda | David W Grainger | Mohamed Abou-El-Enein | Elliott A Gruskin | D. Grainger | G. Duda | M. Abou-el-Enein
[1] Chi-Ping Day,et al. Preclinical Mouse Cancer Models: A Maze of Opportunities and Challenges , 2015, Cell.
[2] Shein-Chung Chow,et al. Adaptive clinical trial design. , 2014, Annual review of medicine.
[3] Andrew L. Kung,et al. A murine lung cancer co-clinical trial identifies genetic modifiers of therapeutic response , 2012, Nature.
[4] Richard Simon,et al. Genomic biomarkers in predictive medicine. An interim analysis , 2011, EMBO molecular medicine.
[5] Larry Rubinstein,et al. Phase 0 Clinical Trials: Conceptions and Misconceptions , 2008, Cancer journal.
[6] Georg N Duda,et al. Qualifying stem cell sources: how to overcome potential pitfalls in regenerative medicine? , 2016, Journal of tissue engineering and regenerative medicine.
[7] Christie M. Ballantyne,et al. Lipid lowering with PCSK9 inhibitors , 2014, Nature Reviews Cardiology.
[8] Janet Woodcock,et al. Expediting drug development--the FDA's new "breakthrough therapy" designation. , 2013, The New England journal of medicine.
[9] C. Mehta,et al. The future of drug development: advancing clinical trial design , 2009, Nature Reviews Drug Discovery.
[10] Jong-Myon Bae,et al. Value-based medicine: concepts and application , 2015, Epidemiology and health.
[11] M Liebsch,et al. Lessons learned from validation of in vitro toxicity test: from failure to acceptance into regulatory practice. , 2001, Toxicology in vitro : an international journal published in association with BIBRA.
[12] Ulrich Dirnagl,et al. Distinguishing between Exploratory and Confirmatory Preclinical Research Will Improve Translation , 2014, PLoS biology.
[13] Petra Reinke,et al. Gene therapy: a possible future standard for HIV care. , 2015, Trends in biotechnology.
[14] B. Ruggeri,et al. Animal models of disease: pre-clinical animal models of cancer and their applications and utility in drug discovery. , 2014, Biochemical pharmacology.
[15] Petra Reinke,et al. Putting a price tag on novel autologous cellular therapies. , 2016, Cytotherapy.
[16] U. Dirnagl,et al. Biomedical research: increasing value, reducing waste , 2014, The Lancet.
[17] Brian D. Wright,et al. Patents versus patenting: implications of intellectual property protection for biological research , 2009, Nature Biotechnology.
[18] Gopi Shankar,et al. A risk-based bioanalytical strategy for the assessment of antibody immune responses against biological drugs , 2007, Nature Biotechnology.
[19] V. Drozdoff,et al. Licensing biotech intellectual property in university-industry partnerships. , 2015, Cold Spring Harbor perspectives in medicine.
[20] Kwok-Kin Wong,et al. New cast for a new era: preclinical cancer drug development revisited. , 2013, The Journal of clinical investigation.
[21] Petra Reinke,et al. The business case for cell and gene therapies , 2014, Nature Biotechnology.
[22] Marcus J Schultz,et al. Critical factors in the translation of improved antimicrobial strategies for medical implants and devices. , 2013, Biomaterials.
[23] Mohamed Abou-El-Enein,et al. Deciphering the EU clinical trials regulation , 2016, Nature Biotechnology.
[24] Jacqueline Corrigan-Curay,et al. Genome Editing Technologies: Defining a Path to Clinic: Genomic Editing: Establishing Preclinical Toxicology Standards, Bethesda, Maryland 10 June 2014. , 2015, Molecular therapy : the journal of the American Society of Gene Therapy.
[25] Marcus J Schultz,et al. Biomaterial-Associated Infection: Locating the Finish Line in the Race for the Surface , 2012, Science Translational Medicine.
[26] Brian A. Nosek,et al. Power failure: why small sample size undermines the reliability of neuroscience , 2013, Nature Reviews Neuroscience.
[27] Pamela A Shaw,et al. Chimeric antigen receptor T cells for sustained remissions in leukemia. , 2014, The New England journal of medicine.
[28] R G Richards,et al. Challenges in linking preclinical anti-microbial research strategies with clinical outcomes for device-associated infections. , 2014, European cells & materials.
[29] David W Grainger,et al. Critical analysis of 3-D organoid in vitro cell culture models for high-throughput drug candidate toxicity assessments. , 2014, Advanced drug delivery reviews.
[30] Petra Reinke,et al. A roadmap toward clinical translation of genetically-modified stem cells for treatment of HIV. , 2014, Trends in molecular medicine.
[31] Emil D Kakkis,et al. Accessing the accelerated approval pathway for rare disease therapeutics , 2016, Nature Biotechnology.
[32] S. Alzghari,et al. Meta-analysis of clinical and preclinical studies comparing the anticancer efficacy of liposomal versus conventional non-liposomal doxorubicin. , 2016, Journal of controlled release : official journal of the Controlled Release Society.
[33] Lee Harland,et al. Lowering industry firewalls: pre-competitive informatics initiatives in drug discovery , 2009, Nature Reviews Drug Discovery.
[34] Ivan Rusyn,et al. In vitro models for liver toxicity testing. , 2013, Toxicology research.
[35] Mark Kessel,et al. The problems with today's pharmaceutical business—an outsider's view , 2011, Nature Biotechnology.
[36] G. Vaidyanathan. Redefining Clinical Trials: The Age of Personalized Medicine , 2012, Cell.
[37] Stuart A. Lipton,et al. Partnering with Big Pharma—What Academics Need to Know , 2016, Cell.
[38] Sylvie Chabaud,et al. Experimental designs for small randomised clinical trials: an algorithm for choice , 2013, Orphanet Journal of Rare Diseases.
[39] Emily S. Sena,et al. Bringing rigour to translational medicine , 2014, Nature Reviews Neurology.
[40] Ali Khademhosseini,et al. Organs-on-a-chip: a new tool for drug discovery , 2014, Expert opinion on drug discovery.
[41] David W Grainger,et al. Cell-based drug testing; this world is not flat. , 2014, Advanced drug delivery reviews.