Trial Design & Conduct Apps
Contact
- Biostatistics Education irvinginst_berd_edu@cumc.columbia.edu
The trial and conduct apps allow users to upload a dataset and assign the next dose or determine the maximum tolerated dose. The apps contain descriptions of the required data as well as sample datasets.
CRM Conduct
- Assign next dose and estimate MTD using CRM
The Continual Reassessment Method (CRM) is a model-based design for phase I trials which aims to find the maximum tolerated dose of a new therapy.

PRO-CRM Conduct
- Assign next dose and estimate MTD using PRO-CRM
Patient-Reported Outcomes Continual Reassessment Method (PRO-CRM) incorporates both clinician and patient perspective to estimate the maximum tolerated dose.

TiTE-CRM Conduct
- Assign next dose and estimate MTD using TiTE-CRM
Time-to-Event Continual Reassessment Method (TiTE-CRM) accounts for the timing of late-onset toxicities and results in shorter trial duration.

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If your research has benefited from one or more Irving Institute resources, please remember to:
- Cite our CTSA grant in any relevant publications, abstracts, chapters, and/or posters.
- Submit your publications to PubMed Central (PMC) for compliance with the NIH Public Access Policy.
- Share your research updates with us by sending an email to: irving_institute@cumc.columbia.edu


