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Updated: Jun 2, 2025

Generation of Comprehensive Thoracic Oncology Database - Tool for Translational Research
Published on: January 22, 2011
Development, Review, and Activation of Thoracic Oncology Investigator-Initiated Trials
David E Gerber1, Claire R Wynters2, Tanushree Prasad1
1Harold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, Texas.
Purpose:
Investigator-initiated trials (IIT) may address important biological and clinical questions that may not be prioritized by pharmaceutical sponsors. However, little is known about the process by which IIT proposals are evaluated and activated.
Experimental Design:
We performed a retrospective study of IIT concepts submitted through the Academic Thoracic Oncology Medical Investigators Consortium, which comprises 13 institutions in the United States and Canada, from consortium inception in 2014 to 2024. We compared approved and disapproved concepts using χ2 tests, Fisher exact tests, and Wilcoxon rank-sum tests.
Results:
Among 68 presented IIT concepts, 60 (88%) received consortium approval a median of 30 days (IQR, 31-59 days) after submission. Concepts submitted by junior faculty were more likely to be approved than those from full professors (P = 0.003). Of the 60 concepts subsequently submitted to pharmaceutical sponsors, 15 (25%) were approved, 43 (72%) were disapproved, and 2 (3%) remain under review. The median time between concept submission to a sponsor and the sponsor's decision was 61 days (IQR, 31-183 days). Concepts with shorter projected durations were more likely to be approved by the pharmaceutical sponsor (P = 0.05). For sponsor-approved IIT concepts, the median overall time from initial submission to trial activation was 18 months.
Conclusions:
Only a small proportion of proposed investigator-initiated cancer clinical trials are successfully activated following a prolonged development process. Given the importance of IITs in addressing real-world, practical questions and the growing professional challenges facing clinical research physician faculty, further attention to IIT development facilitators and barriers is warranted.
Insights
Investigator-initiated trials (IITs) face activation challenges. While consortium approval is high, pharmaceutical sponsor approval is low, leading to prolonged development times for cancer clinical trials.
Area of Science:
- Oncology
- Clinical Trials
- Investigator-Initiated Trials
Background:
- Investigator-initiated trials (IITs) address critical research questions often not prioritized by pharmaceutical sponsors.
- The evaluation and activation processes for IIT proposals are not well understood.
- IITs are vital for exploring practical, real-world clinical questions.
Purpose of the Study:
- To evaluate the process of IIT concept evaluation and activation.
- To identify factors influencing the approval of IIT proposals by a consortium and pharmaceutical sponsors.
Main Methods:
- Retrospective study of 68 IIT concepts submitted to the Academic Thoracic Oncology Medical Investigators Consortium (2014-2024).
- Comparison of approved vs. disapproved concepts using statistical tests (χ2, Fisher exact, Wilcoxon rank-sum).
- Analysis of subsequent pharmaceutical sponsor review outcomes and activation timelines.
Main Results:
- 88% of IIT concepts received consortium approval within a median of 30 days.
- Concepts from junior faculty were more likely to be approved by the consortium.
- Only 25% of consortium-approved concepts were subsequently approved by pharmaceutical sponsors, with a median decision time of 61 days.
- Shorter projected trial durations correlated with higher sponsor approval rates.
- Median time from initial submission to trial activation was 18 months for sponsor-approved IITs.
Conclusions:
- A small fraction of proposed investigator-initiated cancer clinical trials are successfully activated.
- The IIT development process is lengthy and presents challenges.
- Further research into facilitators and barriers for IIT development is warranted.
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