COVID-19: How EMA fast-tracks development support and approval of medicines and vaccinesAlahari, AnuradhaBenstetter, MonikaMedical Writing
Despite its long history, targeted radionuclide therapy (TRT) has only recently attracted attention as a main contributor to cancer therapy. The recent USA Food and Drug Administration and European Medicines Agency approval of two new innovative TRTs was based on phase 3 clinical trial data that de...
All authors take responsibility for the scientific integrity of the work. All authors have read the final version of the manuscript and agreed to the decision to publish. Corresponding author Correspondence to Najia Ahmadi. Ethics declarations Ethics approval and consent to participate The SATURN ...
2023), and does not take into consideration the role of the real cultural context in which individuals live. This paper, however, expands the framework of MOA by incorporating face consciousness—a characteristic of Chinese culture—as an important moderating variable. By doing so, this paper not...
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In case of long-lived proteins, the use of an mRNA expression platform has no apparent impact on the duration of the therapeutic effect, but mRNA half-life does contribute to peak levels expression. Also the size of the antibody molecule restricts its applicability in mRNA form. For example,...
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The same quantity is used by the European Medicines Agency (EMA) as is target threshold. Other sources propose using a limit of 1.5 µg per day.11, 12Quality Control in an E&L StudyStringent quality control measures should be used to confirm the reliability and accuracy of an E&L study....
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“I think of myself as someone who generally thinks carefully about the health consequences of my food choices”, and “I think of myself as someone who generally thinks carefully about the long-term effects of my food choices” (7-point Likert scale from ‘Strongly disagree’ to ‘Strongly...