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Clinical Endpoint Bioequivalence Study
2014The goal of the clinical endpoint bioequivalence study is to perform a comparison of clinical effects of a test and reference drug in order to infer bioequivalence. The clinical endpoint bioequivalence study is a complex compromise method of determining bioequivalence of products that cannot be evaluated by means of a pharmacokinetic or pharmacodynamic
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Surrogate Endpoints in Clinical Trials
Drug Information Journal, 1996Surrogate endpoints are used to document treatment effects more easily and rapidly, yet controversies arise in their use.
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Clinical Trials: New Endpoints
1999Background. The Western community is currently increasingly involved in the problems of patients with chronic diseases. The wish to deal with such problems gives rise to new endpoints in medical research.
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[Intermediate endpoints in clinical research].
Nederlands tijdschrift voor geneeskunde, 2014An intermediate variable such as blood pressure is part of the causal pathway of mechanisms to a clinical outcome, e.g. myocardial infarction. An intervention affects a clinical outcome through its effect on that intermediate variable. In studies designed to assess the effects of interventions an intermediate variable may be used as surrogate for ...
Sanne A E, Peters +2 more
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Composite endpoints in clinical trials
Οι κλινικές δοκιμές αποτελούν μια θεμελιώδη διαδικασία για την αξιολόγηση της αποτελεσματικότητας νέων θεραπειών. Ωστόσο, σε πολλές περιπτώσεις, ένα μόνο πρωτεύον τελικό σημείο δεν επαρκεί για την πλήρη καταγραφή του θεραπευτικού οφέλους, ειδικά όταν τα κλινικά συμβάντα είναι σπάνια, απαιτούν παρατεταμένη παρακολούθηση ή αποτυπώνουν μόνο ένα μέρος του ...Kanellakopoulou, Adamantia +1 more
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Surrogate endpoints in clinical trials
Controlled Clinical Trials, 1985Lawrence Friedman, Salim Yusuf
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Compound endpoints in clinical trials
Controlled Clinical Trials, 1986Michael Terrin, Sandra Forman
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