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In Silico Clinical Trials for Cardiovascular Disease
Published on: May 27, 2022
Clinical trials in jeopardy
G C J M Cleophas1, T J Cleophas
1Faculty of Law, Department of Health Affairs, Erasmus University, Rotterdam, Netherlands. cleophas@frg.eur.nl
Background:
The controlled clinical trial, the gold standard for clinical research, is in jeopardy. The pharmaceutical industry is rapidly expanding its command over clinical trials but scientific rigor requires independence and objectivity. Safeguarding such criteria is hard because industrial sponsors, benefit directly from favorable results and are virtually in complete control.
Objective:
To review flawed procedures jeopardizing the credibility of trials and to look for possible solutions to the conflict between sponsored industry and scientific independence.
Results:
Flawed procedures jeopardizing current clinical trials can be listed as follows. Industries, at least in Europe, are allowed to choose their own independent protocol review board prior for approval. The independent protocol review board approves protocols even when the research is beyond the scope of its expertise. Health institutions hosting multicenter trials are requested to refrain from scientific or ethic assessment of the trial. Trial monitors are often employees of industry. Data control is predominantly in the hands of the sponsor. Interim analyses are rarely performed by independent groups. The scientific committee of the trial consists largely of prominent but otherwise uninvolved physicians attached to the study. The analysis and report of the trial is generally provided by clinical associates of the pharmaceutical companies and, after a brief review, co-signed by prominent physicians attached to the study. POSSIBLE SOLUTIONS: Possible solutions to the conflict between sponsored industry and scientific independence could include the following. Surveillance by independent observers during each stage of the trial is desirable. In contrast, tight control of study data, analysis, and interpretation by the commercial sponsor is undesirable. If, instead, the pharmaceutical industry allows the profession to more actively participate in different stages of the trial, scientific research will be better served, reasonable biological questions will be better answered, and, because the profession will be more convinced of the objective character of the research, it will not be counterproductive to the sales.
Insights
Pharmaceutical industry influence threatens clinical trial integrity. Solutions involve greater physician participation and independent oversight to ensure objective research and reliable results.
Area of Science:
- Clinical research methodology
- Pharmaceutical industry influence
- Scientific integrity
Background:
- Controlled clinical trials are crucial for medical research but face threats to their objectivity.
- The pharmaceutical industry's increasing control over trials raises concerns about scientific rigor and independence.
- Sponsorship bias is a significant challenge due to industry's direct benefit from favorable outcomes.
Purpose of the Study:
- To identify flawed procedures that compromise clinical trial credibility.
- To explore solutions for balancing industry sponsorship with scientific independence.
Main Methods:
- Review of current practices in clinical trial management and oversight.
- Analysis of potential conflicts of interest in industry-sponsored research.
- Identification of procedural vulnerabilities in protocol review, data control, and reporting.
Main Results:
- Flawed procedures include industry selection of review boards, limited institutional ethical assessment, industry-employed monitors, and sponsor control over data.
- Independent interim analyses and objective reporting are infrequent.
- Scientific committees often lack deep involvement, and trial reports may be influenced by industry associates.
Conclusions:
- Greater physician involvement in all trial stages can enhance research objectivity and credibility.
- Independent oversight and data control are essential to mitigate bias.
- Collaborative approaches benefit scientific advancement and public trust in pharmaceutical research.
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