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Jennifer E. Miller

Researcher at Yale University

Publications -  20
Citations -  153

Jennifer E. Miller is an academic researcher from Yale University. The author has contributed to research in topics: Medicine & Clinical trial. The author has an hindex of 3, co-authored 14 publications receiving 44 citations.

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Registration, results reporting, and publication bias of clinical trials supporting FDA approval of neuropsychiatric drugs before and after FDAAA: a retrospective cohort study.

TL;DR: The enactment of FDAAA was followed by significantly higher proportions of trials that were registered and reporting results on ClinicalTrials.gov and significantly lower degrees of publication bias among trials supporting recent FDA approval of drugs for neuropsychiatric indications.

Access to COVID-19 Vaccines in High-, Middle-, and Low-Income Countries Hosting Clinical Trials.

TL;DR: In this article, the authors conducted a cross-sectional study examining the authorization or approval and delivery for COVID-19 vaccines recommended by the World Health Organization (WHO) in the countries where they were tested.
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Racial Privilege and Medical Student Awards: Addressing Racial Disparities in Alpha Omega Alpha Honor Society Membership.

TL;DR: Because of the importance placed on AOAmembership, racial/ethnic membership imbalances could represent a form of structural racism and have profound implications for students, patients, medical research, and the diversity of the healthcare workforce.
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Evaluation of Drug Trials in High-, Middle-, and Low-Income Countries and Local Commercial Availability of Newly Approved Drugs.

TL;DR: In this article, a cross-sectional analysis of trials supporting FDA approval of novel drugs in 2012 and 2014, sponsored by large drug companies, did not involve human participants, and the settings were the countries hosting trials supporting US drug approval.
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Reporting of Study Participant Demographic Characteristics and Demographic Representation in Premarketing and Postmarketing Studies of Novel Cancer Therapeutics.

TL;DR: In this paper, the authors compared the reporting of demographic data and the representation of individuals by sex, age, and race in premarketing and post-marketing studies used by the Food and Drug Administration (FDA) to evaluate novel cancer therapeutics.