[5] The interoperability between the Spanish version of the International Classification of Diseases and ORPHAcodes: towards better identification of rare diseases. Rico J, Echevarría-González de Garibay LJ, García-López M, Guardiola-Vilarroig S, Maceda-Roldán LA, Zurriaga Ó, Cavero-Carbonell...
Both EMA and its U.S. equivalent, the FDA, mention on Wegovy's label that semaglutide causes thyroid tumours in rodents but say the effects on humans are unknown. The FDA advises against taking Wegovy if the patient has a family history of thyroid cancer. ...
Another common misconception is that AI models are continuously retrained in real-time based on user interactions and feedback. In practice, this is quite limited. AI algorithms are typically deployed in specific versions that are periodically updated. A hospital may receive a new version of the ...
MS, MN, JWW, DE, and DFW drafted the first version of the manuscript. All authors contributed intellectually to data interpretation, finalized and approved the manuscript for publication. JWW and DFW secured funding for the study. Corresponding author Correspondence to Julia W. Wu....
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Overall survival was defined as the interval from the date of initial surgical resection to the date of death. The mean follow-up duration of the patients was 34.2 months. All statistical analyses were performed using the SPSS software (version 21.0; IBM Statistics, Armonk, NY). All ...
For more information, see the Summary of Product Characteristics (also part of the EPAR).How does Yondelis work? The active substance in Yondelis, trabectedin, is an anticancer medicine. It is a synthetic version of a substance that was originally extracted from a species of tunicate or ‘sea...
The statistical analysis and visualization were carried out primarily using R (version 4.2.2), and some statistical analyses were carried out using by GraphPad Prism 9 software (GraphPad Software, Inc.). Enumeration data was analyzed by Chi-square test or Fisher’s precision probability test. The...
“Achieving another key regulatory milestone so soon after theU.S.FDA’s acceptance of our New Drug Applications for lenacapavir for PrEP underscores the great interest in how this medication, if approved, could help transform efforts to end the HIV epidemic globally,” saidDietmar Berger...
Will they still be valid and can one still compare them to the results obtained with the new version of the algorithm? Usability and integration How can the application be integrated into your clinical workflow? Ideally, the data processing should take place in the background and be fast ...