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Pharmacokinetics of oral pridinol: Results of a randomized, crossover bioequivalence trial in healthy subjects
Objectives: To establish the relative bioavailability and to assess bioequivalence of oral, immediate-release tablets containing pridinol and to determine the pharmacokinetic properties of the compound. Methods and materials: In this single-center, open-label, randomized, crossover trial, healthy ma...
Uloženo v:
| Vydáno v: | Int J Clin Pharmacol Ther |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Dustri-Verlag Dr. Karl Feistle
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8167741/ https://ncbi.nlm.nih.gov/pubmed/33835016 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5414/CP203900 |
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