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Complete
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the following procedure for a Complete trial if it includes an Investigational New Drug (IND) or Investigational Device Exemption (IDE) as per US Food and Drug Administration regulations. If the trial was registered without IND/IDE information, you can provide it here. IND/IND information is optional for Abbreviated trials.
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The choice of values for some fields in this section depend on values that you have selected in preceding fields. For example, if the IND/IDE Type is "IND", the Grantor must be either "CDER" or "CBER". Further, if the Grantor is either "CDER" or "CBER", and the Holder type is anything other than "NIH" or "NCI", NIH Institution / NCI Division/Program names are not available for selection.
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Before you begin abstracting or validating any trial, be sure you check it out first. Otherwise you will not be able to modify any trial data. |
How to Abstract IND/IDE Information
Search for the trial of interest. For instructions, refer to Searching for Trials in PA.
In the search results, click the NCI Trial Identifier link for that trial. The Trial Identification page appears.
On the Trial Identification page, check out the trial. For instructions, refer to Checking In and Checking Out Trials. (This checkout step is optional for Super Abstractors.)
On the Administrative Data menu, under Regulatory Information, click Trial IND/IDE. The Trial IND/IDE page appears. The IND/IDE Information section lists any IND/IDE records for the trial.
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To add an IND/IDE record
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:
Click Add. The Add IND/IDE section displays IND/IDE data fields.
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In the drop-down lists and text fields, select or enter the appropriate information. The following table describes the fields. An asterisk (*) indicates a required field.
Field Label
Description/Instructions
IND/IDE Type*
Indicate the type of protocol.
Number*
Type the IND/IDE number.
Grantor*
Select the grantor from the drop-down list.
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- If you selected IND, valid values are as follows:
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- CDER – Center for Drug Evaluation and Research
- CBER – Center for Biologics Evaluation and Research
- If you selected IDE, valid values are as follows:
- CDRH – Center for Devices and Radiological Health
- CBER – Center for Biologics Evaluation and Research
Holder Type*
Select the holder type from the drop-down list.
- Do one of the following:
- If you selected
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- either NIH or NCI for the Holder Type, proceed to the next step.
In the drop-down lists and text fields, select or enter the appropriate information. The following table describes the fields. An asterisk (*) indicates a required field.
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Field Label
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Description/Instructions
- Otherwise, skip the next step.
In the NIH Institution / NCI Division/Program
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list, select an appropriate value:
If the holder type is NIH, select the associated NIH institution. For a list of valid values,
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refer to NIH Institution Code Values.
Anchor indcode indcode If the holder type is NCI, select the associated NCI Division
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/Program. For a list of valid values,
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refer to NCI Division
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In the drop-down lists and text fields, select or enter the appropriate information. The following table describes the fields. An asterisk (*) indicates a required field.
Field Label
Description/Instructions
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Availability of Expanded Access*
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Indicate whether or not the drug or device is available outside any clinical trial protocol.
Include Page IND IDE Availability of Expanded Access field - Include 20170414 IND IDE Availability of Expanded Access field - Include 20170414 Expanded Access Record
Include Page IND IDE Expanded Access Record field - Include 20170414 IND IDE Expanded Access Record field - Include 20170414
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Expanded Access Record*
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- Click Save. The system adds the IND/IDE record
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- to the list of existing records.
- To make changes to a record, click the Edit (pencil) icon in the Edit column next to the record you want to modify, and make changes in the Add IND/IDE
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- section.
- To delete
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- one or more records:
- Select the record or records you want to delete (click the check box in the Delete column
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- or click Select All).
- Click Delete
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- .