Nicholas Harrison

Nicholas Harrison
Duke University | DU · Margolis Center for Health Policy

Master of Public Health

About

6
Publications
275
Reads
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126
Citations
Additional affiliations
March 2018 - present
Duke University
Position
  • Research Assistant
September 2016 - January 2018
Boston University
Position
  • MPH Candidate; Health Policy & Law and Pharmaceuticals
September 2013 - June 2015
Boston University
Position
  • Graduate Student, Pharmacology

Publications

Publications (6)
Article
The US Food and Drug Administration (FDA) Biosimilars Guidance describes how biosimilars may be approved based on clinical pharmacokinetic (PK) and pharmacodynamic (PD) biomarker data, without comparative clinical studies with efficacy endpoints. This type of clinical development program, however, has only been implemented for a small number of FDA...
Article
Elevated blood pressure increases the risk of adverse cardiovascular events and death. Accordingly, characterizing the off-target blood pressure effects of drugs is an important component of regulatory benefit-risk assessment and post-marketing clinical decision-making. The U.S. Food and Drug Administration (FDA) released draft guidance in May 2018...
Chapter
Insights concerning leukemic pathophysiology have been acquired in various animal models and further efforts to understand the mechanisms underlying leukemic treatment resistance and disease relapse promise to improve therapeutic strategies. The zebrafish (Danio rerio) is a vertebrate organism with a conserved hematopoietic program and unique exper...
Article
Full-text available
Ethanol abuse during adolescence may significantly alter development of the prefrontal cortex which continues to undergo structural remodeling into adulthood. Glutamatergic neurotransmission plays an important role during these brain maturation processes and is modulated by ethanol. In this study, we investigated glutamate dynamics in the medial pr...
Article
Full-text available
Accumulating evidence indicates that human natural killer (NK) cells develop in secondary lymphoid tissue (SLT) through a so-called "stage 3" developmental intermediate minimally characterized by a CD34(-)CD117(+)CD94(-) immunophenotype that lacks mature NK cell function. This stage 3 population is heterogeneous, potentially composed of functionall...

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