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Comment: For CTRPMICRO-91, revised based on review feedback from Michael Izbicki.

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If you import an Expanded Access trial from ClinicalTrials.gov (whether via the Registration or PA web application), the system automatically sets this value to Yes. Otherwise, the default is No. The system does not include this attribute in the TSR, in the XML output to ClinicalTrials.gov, in the trial data sent to Cancer.gov, or in the set of trials provided to the NCI Clinical Trials API. 

When a trial has trial is listed as Expanded Access at the trial level in CTRP, the Expanded Access use of the drug/device will most likely require be required by another interventional trial with an IND/IDE that is Available for Expanded Access. For instructions on configuring the separate Expanded Access fields for the trial with an as part of the IND/IDE for a trial, refer to to Abstracting INDs and IDEs. Consider also Also, consider specifying each of these trials as an Associated Trial for the other. For instructions, refer to Associating Trials.