Laboratory data in healthy volunteers: reference values, reference changes, screening and laboratory adverse event limits in Phase I clinical trials-Reference-Cited by-同舟云学术

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Laboratory data in healthy volunteers: reference values, reference changes, screening and laboratory adverse event limits in Phase I clinical trials

Published:1999-03-17 Issue:1 Volume:55 Page:13-19
ISSN:0031-6970
Container-title:European Journal of Clinical Pharmacology
language:
Short-container-title:European Journal of Clinical Pharmacology

Author:

Sibille M.,Deigat N.,Durieu I.,Guillaumont M.,Morel D.,Bienvenu J.,Massignon D.,Vital Durand D.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s002280050586.pdf

Cited by 13 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Data driven evaluation of healthy volunteer characteristics at screening for phase I clinical trials to inform on study design and optimize screening processes;Clinical and Translational Science;2021-08-11

2. Hypokalzämie, Hypophosphatämie und Hypomagnesiämie;Journal für Gynäkologische Endokrinologie/Schweiz;2021-03-23

3. Consensus Guidelines: Best Practices for Detection, Assessment and Management of Suspected Acute Drug-Induced Liver Injury During Clinical Trials in Adults with Chronic Viral Hepatitis and Adults with Cirrhosis Secondary to Hepatitis B, C and Nonalcoholic Steatohepatitis;Drug Safety;2020-11-03

4. Establishment of reference intervals of biochemical analytes for healthy Chinese volunteers during the screening process in clinical pharmacology trials;European Journal of Clinical Pharmacology;2020-06-03

5. EASL Clinical Practice Guidelines: Drug-induced liver injury;Journal of Hepatology;2019-06

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