Ensuring Transparency and Quality of Clinical Trial Reporting in Clinical Pharmacology & Therapeutics: Prospective Trial Registration and Compliance with Reporting Guidelines Are Required for all Clinical Trials

Author:

Smith D. Max12ORCID,Minichmayr Iris K.3ORCID,Standing Joseph F.45ORCID,Giacomini Kathleen M.6ORCID,van der Graaf Piet H.78,Peck Richard W.910ORCID

Affiliation:

1. MedStar Health Columbia Maryland USA

2. Department of Oncology Georgetown University Medical Center Washington DC USA

3. Department of Clinical Pharmacology Medical University of Vienna Vienna Austria

4. Great Ormond Street Institute of Child Health University College London London UK

5. Department of Pharmacy Great Ormond Street Hospital for Children London UK

6. Department of Bioengineering and Therapeutic Sciences University of California San Francisco San Francisco California USA

7. Certara Canterbury UK

8. University of Leiden Leiden The Netherlands

9. Department of Pharmacology & Therapeutics University of Liverpool Liverpool UK

10. Pharma Research & Development (pRED) Roche innovation Center Basel Switzerland

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Reference21 articles.

1. Outcome pre-specification requires sufficient detail to guard against outcome switching in clinical trials: a case study

2. Clinical trial registration: a statement from the International Committee of Medical Journal Editors (accessed Sep 19 2023).

3. Recommendations for the Conduct Reporting Editing and Publication of Scholarly Work in Medical Journals (accessed Sep 19 2023).

4. Clinical Trials Registration: Frequently asked questions (accessed Sep 19 2023).

5. World Health Organization – International Clinical Trials Registry Platform (ICTRP) (accessed Sep 19 2023).

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