Streamlining and cycle time reduction of the startup phase of clinical trials

Author:

Abu-Shaheen Amani,Al Badr Ahmad,Al Fayyad Isamme,Al Qutub Adel,Faqeih Eissa Ali,Al-Tannir Mohamad

Abstract

Abstract Objective The startup phase of a clinical trial (CT) plays a vital role in the execution of new drug development. Hence, the aim of this study is to identify the factors responsible for delaying the CT startup phase. Further, it focuses on streamlining and reducing the cycle time of the startup phase of newly sponsored CTs. Methods Thirteen sponsored CTs conducted between 2016 and 2017 at the Clinical Research Department of King Fahad Medical City, Riyadh, Saudi Arabia, were considered for this study. Eight trials were analyzed to identify the data specific to startup metrics using the FOCUS–PDCA cycle (Find an improvement area–Organize a team–Clarify current practices–Understand the source of variation/problem–Select a Strategy–Plan–Do–Check–Act). Six measures incorporated in the metrics were (1) date of initial contact with site to the signing of confidentiality agreement, (2) date of receiving questionnaire from sponsor to date of its completion, (4) time taken to review protocol and approve investigational drug service form, and (5) time taken to study protocol and approve pharmacy and pathology and clinical laboratory medicine form and date of receipt of institutional review board (IRB) submission package to final IRB approval. Fishbone analysis was used to understand the potential causes of process variation. Mean (SD) time was calculated for each metric before and after implementation of the intervention protocol to analyze and compare percentage reduction in the mean cycle time of CTs. Data were represented as mean (SD), and the P value was calculated for each metric. The significance level was set at P < 0.05. Results Of the various potential factors of delay identified through fishbone analysis, the two major ones were lack of a well-defined timeline for approval and review of the study protocol and inconsistent IRB meetings. After introduction of the new intervention protocol, the entire CT life cycle was reduced by 45.6% (mean [SD], 24.8 [8.2] weeks vs. 13.5 [11.6] weeks before and after the intervention, respectively). Conclusion Various factors are responsible for the delay of the startup phase of CTs, and understanding the impact of each element allows for optimization and faster execution of the startup phase of CTs.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Medicine (miscellaneous)

Reference17 articles.

1. Novitzke JM. The significance of clinical trials. J Vasc Interv Neurol. 2008;1:31.

2. Toerien M, Brookes ST, Metcalfe C. A review of reporting of participant recruitment and retention in RCTs in six major journals. Trials. 2009;10:52.

3. Giffin RB, Lebovitz Y, English RA, editors. Transforming clinical research in the United States: challenges and opportunities: workshop summary. Washington, DC: National Academies Press; 2010.

4. Abozguia K, Phan TT, Shivu GN, Maher A, Ahmed I, et al. Insights into how to conduct a clinical trial in the UK. J R Soc Med. 2007;100:469–72.

5. Schimanski C. Streamline and improve study start-up. Appl Clin Trials. 2013;22:22–5.

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